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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
031458 Machine Tender (N) (Open)
Job Description:
Key Responsibilities
* Routinely clean and lubricate equipment, maintain a manufacturing area free from debris and dirt, ready or put away tools as assigned.
* Closely follows directions to operate machinery, hold or supply routine materials and tools, and load or unload items on machinery and assembly lines.
* Performs routine property care activities.
* Performs any non-technical routine tasks at the plant.
* Routine quality checks on finished products.
* Reports any issues to supervisor or higher-level colleague.
* Follow safety regulations.
* Performs other duties as assigned.
Education and Experience
* Typically possesses a high school diploma (or equivalent).
Knowledge and Skills
* Basic verbal and written communication skills.
* Ability to listen, understand, and follow directions.
* Ability to work in a variety of roles.
Compensation Range:
The pay range for this position is $15.77 - $26.83.
Typically, a competitive wage for new hires will fall between $15.80 to $15.80.
Offers for this position may vary based on market data and other factors such as job-related knowledge, skills, experience, and geographic location.
If the competitive wage is equal in both fields, the starting rate is the same for all applicants that apply for this role.
The starting rate is not representative of future compensation increases.
The position may also be eligible for a short-term incentive.
Benefits Statement:
Greif offers a comprehensive benefits package, including medical, dental, paid time off, and other competitive benefits which are available for eligible colleagues effective day one.
Protect Yourself From Scams: We value the integrity of our recruitment process and prioritize the well-being of our candidates.
While you may find Greif job postings on various platforms, all legitimate opportunities can be verified on our official Careers page at www.greif.com.
All communication from Greif regarding job opportunities will also come from an @greif.com email address.
If you have concerns about the legitimacy of a job posting, receive an unsolicited job offer or suspect fraudulent activity, please contact us for verification via this link Contact Us - Greif.
EEO Statement:
https://www.greif.com/wp-content/uploads/2023/04/HR-101-Equal-Employment-Opportunity-Policy-English.pdf
We offer a competitive salary, excellent benefits and opportunity for growth.
Greif is an equal opportunity employer.
We will not discriminate against any applicant or employee on the basis of sex, race, religion, age, national origin, color, disability, veteran status or any other any other legally protected characteristic.
For more information read Greif’s Equal Opportunity Policy.
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Type: Permanent Location: Winnipeg, CA-MB
Salary / Rate: Not Specified
Posted: 2025-07-14 08:05:06
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Historically, the role of IT has been to provide a reliable ecosystem to run the business, drive efficiencies and reduce costs.
These areas remain integral, however, driven by the quickening pace of innovation, IT must evolve, proactively partnering with the business to enable new digital business models that power new types of customer engagement.
At Elanco, our engineer roles bring adaptive set of skills covering Software-as-a-Service (SaaS), Commercial-of-the-Shelf (CotS) and/or Custom Developed applications.
The role is part of our software engineering team established to deliver Engineering expertise to business facing products and services.
As an Engineer you will be deployed into a multi-disciplined product team applying your software engineering talent to Elanco’s biggest opportunities.
To be successful in an engineering role in Elanco requires a highly motivated individual, with an innovative mindset and a willingness to drive tangible outcomes.
The individual must be able to articulate complex technical topics and collaborate with the internal engineering organisation to improve engineering across the enterprise.
Your Responsibilities:
Engineering
* Join a diverse engineering organisation and contribute to growing our engineering capabilities across Software, and Platform Engineering.
* Develop full-stack solutions, building highly scalable distributed solutions that enable positive user experiences and measurable business growth.
* Implement and support modern digital products that are technologically sound, avoid technical debt, guarantee compliance, and enable the required business outcome.
* Collaborate with Platform Engineering team to provide input to shaping their products allowing software engineers to deliver business value faster than ever before.
* Look for continuous improvement opportunities in our core ecosystem identifying new ways to enhance application team and developer experience.
* Embed security, privacy, data protection and quality assurance across all digital solutions.
* Build and...
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Type: Permanent Location: Hook, GB-HAM
Salary / Rate: 84000
Posted: 2025-07-14 08:03:06
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What your impact will be:
* Will be responsible for doing all the technical implementations (design, creation, and deployment) for different AWS resources in an automated fashion, using the best practices of security, monitoring, & cost optimization.
* Will be responsible for AWS related solutions, architecture decisions and designing the platform components as well as implementing them
* Will be responsible for writing and deploying these solutions using IaC methodology
* Build and implement a continuous integration and continuous deployment platform
* Automate system, application deployment and management processes - aiming for efficiency!
* Create and maintain alert and monitoring solution to promptly identify and escalate unexpected issues
* Will be responsible for creating documentation for everything Cloud DevSecOps in Confluence
* Must be a self-driven, individual contributor, aware of Agile scrum methodology to participate in project activities.
Daily Task
* Check system monitoring tools for alerts or issues
* Track the status of AWS resources and services
* Review daily AWS cost reports for any unusual spikes
* Fix any issues with AWS Glue jobs or other services
* Write or update Python scripts for automation or data tasks
* Build and maintain AWS infrastructure (servers, storage, etc.)
* Monitor and manage AWS Lambda functions linked to Snowflake
* Manage user access using AWS SSO (add/remove users, update roles)
* Attend daily team meetings and give updates
* Update task trackers like Jira with progress.
Minimum Qualifications:
* 5-7 years’ experience with AWS core (VPC, EC2, S3, IAM, RDS); AWS serverless (API gateway, Lambda, DynamoDB)
* 5-7 years’ experience with big data managed services (Snowflake, Redshift, Data Pipelines, EMR, Step Functions)
* 3+ years’ experience with Control Tower, Landing Zones, Core Services, Service Catalog, Code Commit or other GIT source control, Code Pipeline or Terraform, ECS, EKS, IAM, Jenkins, Ansible, Docker, Terraform/CloudFormation, Amazon ECS/EKS, CloudWatch, Lambda, Route 53, EMR, AWS Glue
* 4+ years’ experience working with containers and container orchestration
* 4+ years’ experience designing CI/CD pipelines
* 3+ years’ experience supporting PostgreSQL or similar relational database technologies
* Must have experience with security tools like Crowdstrike Falcon, Prisma Cloud and Fortigate
* Must have good knowledge of Python and shell scripting
* Must have good knowledge of Networking and Security Concepts
* AWS Certified Solutions Architect
* Must be well versed with Infrastructure solutioning
Additional Qualifications/Bonus:
* Specialized experience with security and compliance, especially with HIPAA, HITRUST, GDPR, CCPA, CPRA
* Healthcare experience would be plus.
Soft Skills
* Good Communication and C...
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Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: 145833.33
Posted: 2025-07-14 08:03:04
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Your Job
Georgia-Pacific Consumer Manufacturing Group is seeking qualified professionals to be considered for our Pulp Processing Engineer role supporting the Consumer Products Group Operations located in Muskogee, OK.
The Muskogee facility uses integrated technology to manufacture tissue, paper towel and napkin products in a progressive production environment.
As a Pulp Processing Process Engineer at Georgia-Pacific, a leading subsidiary of Koch Industries, you would be responsible for optimizing the production processes within pulp and paper manufacturing facilities.
Your role would involve ensuring efficient, safe, and cost-effective operations while maintaining high quality standards.
Our Team
The Muskogee Plant is part of the tissue, towel, and napkin paper products manufacturing operation.
We are proud to safely manufacture quality products that have a competitive advantage and solid growth within the marketplace.
We create a work environment that attracts, engages, and retains the best people.
Our technology is state of the art, and we will bring the best team together to deliver for our customers, Georgia-Pacific, and the Muskogee community.
What You Will Do
* Embrace influential leadership to support the organization while advancing our Principle-Based Management (PBM) culture
* Analyze and improve existing pulp processing operations to increase efficiency, reduce waste, and enhance product quality
* Implement process control strategies and technologies to optimize production
* Lead and support projects aimed at process improvement, equipment upgrades, and new technology implementations
* Collaborate with cross-functional teams to ensure projects are completed on time and within budget
* Gather and analyze process data to identify trends, variances, and areas for improvement
* Prepare detailed reports and present findings to management and other stakeholders
* Ensure all operations comply with environmental, health, and safety regulations
* Develop and implement safety procedures and protocols to prevent accidents and incidents
* Investigate and resolve production issues, implementing corrective actions to prevent recurrence
* Work closely with maintenance teams to minimize downtime and equipment failures
* Promote a culture of continuous improvement by identifying and implementing lean manufacturing and Six Sigma principles
* Train and mentor team members on best practices and new technologies
* Partner with R&D, quality assurance, and other departments to develop new products and improve existing ones
* Engage with suppliers and vendors to negotiate equipment purchases and upgrades
* Learn necessary computer and process control skills related to the processes (PC's, PI data and SAP
Who You Are (Basic Qualifications)
* Experience in a pulp/paper or similar manufacturing environment
* Understanding of pulp and paper processes, equipment, ...
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Type: Permanent Location: Muskogee, US-OK
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:50
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Your Job
Molex is seeking an experienced Senior Automation Controls Project Engineer who will be responsible for the design and development of new High-Speed Custom Automation Electrical Control Systems, Machine Software, and User Interface.
The project engineer's creativity is key to producing easy-to-operate, safe, on-time equipment that will give Molex a competitive advantage in the marketplace.
Our Team
Molex creates connections for life by enabling technologies that transform the future and improve lives.
With a presence in more than 40 countries, Molex offers a complete range of connectivity products, services and solutions for the data communications, medical, industrial, automotive and consumer electronics industries.
Our Datacom and Specialty Solutions (DSS) team designs an extensive product line serving customers in telecommunications, datacom, hyperscalers, cloud, data center and storage applications.
You can check out a highlight of our custom automation team's capabilities here: https://www.youtube.com/watch?v=0gxNyypfzGU
What You Will Do
* Provides controls feasibility and equipment cost estimates to automation development team.
* Works with mechanical engineering department to determine design complete dates.
Prioritizes work to fulfill deadlines.
* Specifies control hardware and generates Bills of Material, designs control panels and enclosures, creates electrical & pneumatic schematics.
* Assists in executing the machine debug, qualification, and installation
* Writes and modifies machine code and builds the HMI to function for plant needs globally.
* Provides technical support for the launch of equipment produced by the DSS tool engineering Team.
Responsibilities will include traveling to mass production facilities for machine installation & qualification, training of technicians and operators to ensure the proper and safe operation of equipment and support any software changes in the field.
* Attends Design Reviews and PFMEA's while working with mechanical engineers to improve current and future designs of automation.
* Tracks projects using internal methods for summarizing component cost, labor, and lead time.
Develops accurate, up-to-date BOM's and Spare Parts Lists
* Performs other related duties as assigned by management.
* International Travel: Up to 15% per year.
Who You Are (Basic Qualifications)
* Associate's degree in electrical engineering or electrical engineering technology
* 7+ years' experience in control panel design
* 7+ years' experience in PLC Programming
* Proficient in Ladder Logic & Motion PLC Programming
* Experience in generating industrial electrical schematics including safety guarding standards
* Experience with high speed synchronous, asynchronous, flexible (robotics) assembly systems.
* Expertise in the design and documentation of machine controls.
* Proven ability to effectively collaborate in a global...
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Type: Permanent Location: Conway, US-AR
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:49
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Molex possesses a rich heritage in the optical industry.
We provide the highest performing field-proven wavelength management solutions from components to modules and integrated line-cards.
Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplifier technology and comprehensive optical, mechanical, electrical and software integration capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks.
Our Optical Solutions team is seekin g a skilled and motivated Product Engineer to join our team and contribute to the design, development, and lifecycle management of optical transceivers.
This role will bridge the gap between R&D, manufacturing, quality, and product management, ensuring high performance, reliability, and manufacturability of optical communication components.
Some travel is expected in this role.
What You Will Do
* Support the development and launch of high-speed optical transceivers (e.g., QSFP, SFP, OSFP) from concept through production.
* Collaborate with cross-functional teams including design, test, process, and reliability engineers to ensure product readiness.
* Define product specifications, support qualification plans, and conduct performance evaluations.
* Interface with manufacturing teams to ensure design for manufacturability (DFM) and resolve production issues.
* Analyze data to monitor product yields, reliability trends, and customer feedback
* Drive root cause analysis and corrective actions for product-related issues.
* Contribute to continuous improvement initiatives for product quality, cost, and performance.
* Provide technical support to customers, sales, and field application engineers.
Who You Are (Basic Qualifications)
* Bachelor's degree in Electrical Engineering, Optical Engineering, Physics, or a related field
* 3+ years of experience in optical transceiver design, testing, or product engineering.
* Strong understanding of optical communication principles, such as modulation formats, link budgets, and fiber optics.
* Experience with high-speed electrical and optical testing (e.g., eye diagrams, jitter, BER testing).
* Familiarity with industry standards (e.g., IEEE 802.3, MSA specs for SFP/QSFP).
* Hands-on experience with lab equipment (oscilloscopes, bit error rate testers, optical spectrum analyzers).
* Solid analytical and problem-solving skills.
* Excellent communication and project management abilities.
* Proficient in data analysis.
* Experience with manufacturing processes and quality systems.
What Will Put You Ahead
* Master's degree in Electrical Engineering, Optical Engineering, Physics, or a related field
For this role, we anticipate paying $130,000- $155,000 per year.
This role is eligible for variable pay, issued as a monetary bonus or in another form.
At Koch companies, ...
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Type: Permanent Location: Fremont, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:49
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Your Job
Georgia-Pacific is currently recruiting for a Large Capital Projects Controls Lead to support the Project Services team for the Corporate Projects and Engineering Group.
This group consists of individuals across the United States working with our manufacturing facilities on capital project execution.
The Large Capital Projects Controls Lead will be responsible for the overall success of the project controls and other services on projects they are assigned.
They will be leading estimating, cost management, overall project reporting, scheduling, risk management, document control, change management, and project best practices.
This person will be a leader that will drive the project controls.
This position is a remote position with travel involved.
The amount of travel would be at least 50% dependent on business needs.
Our Team
Our team is made up of individuals with diverse backgrounds supporting project services capabilities across the Georgia Pacific Organization.
The project Services team builds and strengthens relationships with industry wide partners to successfully execute projects throughout the United States.
Our team comprised of project controls leads and capability leaders supporting project proven practices during front end load through closeout.
What You Will Do
* Lead Project Controls capability on a group of projects in Georgia-Pacific to achieve superior project results
* Responsible to manage the development and implementation of an effective Project Controls capability on a group of projects to support capital project execution, including developing and executing the plan for estimating, scheduling, cost engineering, metrics, reporting, workload resource planning, risk management, document controls, and facilitate best practices sessions.
* Responsible for identifying and implementing project controls tools and enablers, by partnering with the project team
* Responsible for providing change management tools and processes for capital project teams, and additionally supporting the review process of project changes
* Partner with Sourcing to implement strategies and manage relationships with contractors and 3rd party providers of project controls resources
* Ensure project controls talent is sufficient on each project to ensure successful implementation of the Project Controls Plan
* Knowledge share with other leaders across the business to benchmark, identify, and implement innovation opportunities in project controls
* Perform project controls functions during front end loading, including schedule creation, establishing the work breakdown structure, establishing the risk log, ensuring document control structures are established, and facilitating best practice meetings.
* Travel up to 50% of the time to lead and participate in project meetings onsite, in engineering offices, key OEM & Contractor locations, and GP locations.
Who You Are (Basic Qualifications)
* Seven...
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Type: Permanent Location: Green Bay, US-WI
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:47
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Your Job
Georgia-Pacific is currently recruiting for a Large Capital Projects Controls Lead to support the Project Services team for the Corporate Projects and Engineering Group.
This group consists of individuals across the United States working with our manufacturing facilities on capital project execution.
The Large Capital Projects Controls Lead will be responsible for the overall success of the project controls and other services on projects they are assigned.
They will be leading estimating, cost management, overall project reporting, scheduling, risk management, document control, change management, and project best practices.
This person will be a leader that will drive the project controls.
This position is a remote position with travel involved.
The amount of travel would be at least 50% dependent on business needs.
Our Team
Our team is made up of individuals with diverse backgrounds supporting project services capabilities across the Georgia Pacific Organization.
The project Services team builds and strengthens relationships with industry wide partners to successfully execute projects throughout the United States.
Our team comprised of project controls leads and capability leaders supporting project proven practices during front end load through closeout.
What You Will Do
* Lead Project Controls capability on a group of projects in Georgia-Pacific to achieve superior project results
* Responsible to manage the development and implementation of an effective Project Controls capability on a group of projects to support capital project execution, including developing and executing the plan for estimating, scheduling, cost engineering, metrics, reporting, workload resource planning, risk management, document controls, and facilitate best practices sessions.
* Responsible for identifying and implementing project controls tools and enablers, by partnering with the project team
* Responsible for providing change management tools and processes for capital project teams, and additionally supporting the review process of project changes
* Partner with Sourcing to implement strategies and manage relationships with contractors and 3rd party providers of project controls resources
* Ensure project controls talent is sufficient on each project to ensure successful implementation of the Project Controls Plan
* Knowledge share with other leaders across the business to benchmark, identify, and implement innovation opportunities in project controls
* Perform project controls functions during front end loading, including schedule creation, establishing the work breakdown structure, establishing the risk log, ensuring document control structures are established, and facilitating best practice meetings.
* Travel up to 50% of the time to lead and participate in project meetings onsite, in engineering offices, key OEM & Contractor locations, and GP locations.
Who You Are (Basic Qualifications)
* Seven...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:47
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Your Job
Georgia-Pacific Consumer Products Operation is currently seeking a highly motivated and talented individual to join our Muskogee, Oklahoma team as a Process Improvement Engineer role supporting the Consumer Products Group Operations located in Muskogee, OK.
In this role, as a part of our Mill Process Improvement Team, you will have the opportunity to analyze operational processes, identify and lead overall improvement strategies.
Our Process Improvement Engineer at Georgia-Pacific typically focuses on enhancing manufacturing processes to increase efficiency, reduce waste, and improve product quality.
You will work closely with Mill area resources as well as ensure alignment with mill priorities.
If you have a passion for driving process optimization, process waste elimination, manufacturing engineering, cost analysis, process safety, and a curiosity to understand manufacturing and business processes then we invite you to apply for this exciting opportunity.
Our Team
The Muskogee facility is part of the tissue, towel, and napkin paper products manufacturing operation.
We are proud to safely manufacture quality products that have a competitive advantage and solid growth within the marketplace.
We create a work environment that attracts, engages, and retains the best people.
Our employees help other's and the business reach their full potential, promoting our Principle-Based Management culture to the work they do every day.
Our technology is state of the art, and we will bring the best team together to deliver for our customers, Georgia-Pacific, and the Muskogee community.
What You Will Do
* Embrace influential leadership to support the organization while advancing our Principle-Based Management (PBM) culture
* Be an active member of the Mill Process Improvement Team creating a competitive advantage within our facility through execution of Disciplined Operational Processes around:
* Management Systems
* Organization & Talent
* Asset Care
* Operations
Analyze data to identify trends, variances, and opportunities for process improvement, waste reduction and competitive cost opportunities
Facilitate and lead cross-functional teams to identify, develop and implement best practices and process improvements to enhance operational efficiency and effectiveness
Collaborate with mill and/or corporate resources to ensure initiatives are aligned with mill priorities, goals, and objectives
Implement, monitor, and communicate key performance indicators (KPIs) with the Leadership and manufacturing teams
Provide guidance, training, and support to ensure team members achieve their full potential and align with organizational goals
Build tools to support and simplify the mill performance tracking, monitoring, and reporting
Support the financial aspects of manufacturing processes, including budgeting, cost control, and financial analysis
Periodically serve as "Operations Support on call" on a r...
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Type: Permanent Location: Muskogee, US-OK
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:46
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Molex possesses a rich heritage in the optical industry.
We provide the highest performing field-proven wavelength management solutions from components to modules and integrated line-cards.
Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplifier technology and comprehensive optical, mechanical, electrical and software integration capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks.
In Bridgewater NJ, we serve large, global clients in telecom and datacom industries in providing next generation optical modules to support the growing need for data and communications.
We are developing optical connectivity solutions, optoelectronic solutions, Wavelength Selective Solutions assembly and fiber optic assemblies and arrays.
We are looking for a Optical Engineering Manager with a focus on holistic viewpoint of optical systems.
The Optical Engineering Manager leads development of complex free-space optical systems by, generating optical design concept, considering the entire product from optical point of view, solving design issues, optimizing the system design in terms of performance, cost and schedule.
This person must have strong understanding of optical principles and extensive experience in various fields including physics, electronics, mechanical, software, reliability and project management to lead the optical product development effort.
As a principal member of the team, this position is responsible for all the optical aspects of a new product development as well as new technology development activities.
This expertise will lead to the advancement of our products and services in the fields of optical communication.
What You Will Do
* Innovation of optical system design of Molex free space optical systems
* Manage a team of optical engineers for new product development, R&D, manufacturing supports
* Mentor other engineers and cross functional groups on optical engineering
* Conduct thorough analysis of products' optical requirements and specifications
* Plan and manage optical system engineering for product development which requires collaboration with electrical, mechanical, SW, reliability engineering teams
* Monitor and R&D for new technologies and components we can utilize in our products
* Work with marketing team to generate technology development strategy for future product applications
Who You Are (Basic Qualifications)
* Master's degree in Engineering, Physics, Photonics or related technical field.
PhD.
is plus
* At least 15 years of industry experience with free-space optical systems
* Experienced in leading the development of free space optical systems
* Experience in managing a team of engineers
* Familiarity with project management methodologies
* Excellent understanding and experience with optical simulation tools such as Zemax...
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Type: Permanent Location: Bridgewater, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:45
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Molex possesses a rich heritage in the optical industry.
We provide the highest performing field-proven wavelength management solutions from components to modules and integrated line-cards.
Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplifier technology and comprehensive optical, mechanical, electrical and software integration capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks.
In Bridgewater NJ, we serve large, global clients in telecom and datacom industries in providing next generation optical modules to support the growing need for data and communications.
We are developing optical connectivity solutions, optoelectronic solutions, Wavelength Selective Solutions assembly and fiber optic assemblies and arrays.
We are looking for a Principal Optical Engineer with a strong focus on innovative design of optical systems.
The Principal Optical Engineer leads development of complex free-space optical systems by, generating optical design concept, guiding optical engineers, solving design issues, optimizing the design processes.
This person must have strong understanding of optical principles and extensive Zemax experience to lead the optical design effort.
As a principal member of the team and a lead optical designer, this position is responsible for all the optical aspects of a new product development as well as new technology development activities.
This expertise will lead to the advancement of our products and services in the fields of optical communication.
What You Will Do
* Innovation of optical design/architecture of Molex free space optical systems
* Conduct thorough analysis of optical system requirements and specifications
* Create, design and analyze optical architectures in Zemax
* Plan and manage prototyping and characterization of optical designs including DOE plan, alignment plan, test coordination, data analysis
* Utilize advanced simulation tools and modeling techniques to evaluate and optimization the performance of free-space optical systems
* Conduct experimental testing and validation of optical components, including spectral analysis
* Generate technology development ideas for future product applications
* Collaborate with multi-disciplinary design teams to integrate optical systems with other hardware, materials and electrical and mechanical components
* Mentor other engineers and cross functional groups on optical design and engineering
* Develop new tools and techniques as needed to continuously improve our ability to model and understand optical designs accurately
Who You Are (Basic Qualifications)
* Master's degree in Engineering, Physics, Photonics or related technical field.
PhD.
is plus
* At least 15 years of industry experience with free-space optical design
* Experienced in leading the development of fre...
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Type: Permanent Location: Bridgewater, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:45
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We are expanding our in-house Engineering team and are on the lookout for a skilled High-Current Terminal and Cavity Design Engineer to join us.
If you're eager to fast-track your career and become a part of an exceptional company, this opportunity might be perfect for you.
As a High-Current Terminal and Cavity Design Engineer, you will spearhead the development of new terminal and connector products for the automotive industry, guiding them through all stages of the product development lifecycle to transition concepts into production.
Additionally, you will assist with modifications and extension work for existing products and contribute to research and development initiatives within the High-Current automotive sector.
What You Will Do
* Lead automotive High-Current terminal and cavity concept development activities with minimal guidance from the Engineering Manager.
* Collaborate with design engineers to develop 3D models and drawings that adhere to Molex standards and GD&T methodology.
* Plan and lead DFMEAs, FEAs, tolerance analysis, and other theoretical studies.
Develop mitigation plans for areas of risk.
* Direct documentation of the project scope, requirements, feasibility, and engineering work plan.
* Manage material selection and justification, focusing on resins for plastic injection molding and metals for stamping components.
* Develop High-Current Terminal/cavity test plans (DVP&Rs) and evaluate results using statistical methods.
Lead failure analysis using structured problem-solving methods.
* Act as the engineering voice to cross-functional teams and customers, ensuring design objectives are met and identifying/directing R&D opportunities in High-Current connectors.
Who You Are
* Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a related field
* 5 years of product design experience with a depth of knowledge in material, mechanics, manufacturing processes, & engineering processes/tools.
* Experience in managing multiple projects simultaneously.
What Puts You Ahead
* terminal/cavity design and knowledge of resins, metals, engineering tools and processes, and manufacturing processes (injection molding, stamping, plating, assembly).
* 1 or more years in a mentoring role to other design engineers
* Experience with DFMEA, FEA, Tolerance Analysis, GD&T, and other theoretical studies.
* Experience developing test plans (DVP&Rs) and analyzing test results using statistical methods.
Demonstrated ability to follow structured problem-solving methods (8D, 5 Why, Fishbone, etc.) to root cause issues.
* Proven ability to manage project scopes, requirements, and engineering work plans.
At Koch Companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value, and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market da...
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Type: Permanent Location: Rochester Hills, US-MI
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:43
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Your Job
Molex possesses a rich heritage in the optical industry.
We provide the highest performing and field-proven wavelength management solutions from components, modules to integrated line-cards.
Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplification technology and comprehensive optical, mechanical, electrical and software design capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks of telecom, datacom, hyperscale datacenter and supercomputing.
Located in Fremont, California, we are looking for a talented Thermal Mechanical Simulation Engineer to join our team.
The engineer for this position will work with a global multi-disciplined team, including mechanical, electrical, optical, reliability, and production line teams.
What You Will Do
* Do thermal mechanical simulation to support multiple product development in either module or component level.
The simulation includes predictions of temperature and airflow distributions as well as thus induced thermal stress and deformation and provide guidelines for optimization of product designs to meet spec and avoid any reliability issues in terms of temperature, deformation, stress, humidity, electrical force, etc.
* Do static structural simulation to analyze deformation and stress induced by either external forces or environmental temperature changes to guide product design and pass all tests.
* Do other simulations such as seam seal, laser welding, soldering, fatigue, MEMS chip's mechanical performance simulation, opto-mechanical integrated simulation by working together with optical simulation engineers, etc.
* Work with mechanical and electrical design engineers to modify and optimize mechanical layout and electrical PCB layout designs as well as choose proper materials (metal, non-mental, ceramic, glass, epoxy, etc.) to minimize deformation and stress and meet manufacture requirements and the spec.
* Work with reliability engineers to design various reliability tests, verify the reliability performance of product, and pass test for product delivery.
* Help develop new simulation capabilities requested from product developments to solve the issues and problems newly encountered in production.
Who You Are (Basic Qualifications)
* Master or Ph.D.
degree in mechanical engineering or related technical fields or discipline with strong analytical capabilities.
* Solid fundamentals in heat transfer and fluid mechanics.
* At least 2 years working experience in telecommunication industry or other related industries; OR experience in a PhD or Master's Degree program focused on simulation and modeling.
* Proficient in using ANSYS Mechanics, Icepak, Solidworks or SpaceClaim, etc.
* Familiar with mechanical design and be able to create and read 2D/3D model and drawing.
* Eager to learn and have strong ...
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Type: Permanent Location: Fremont, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-14 08:02:13
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Geel, Antwerp, Belgium
Job Description:
Wij zijn opzoek naar het beste talent voor Operator Poeder Unit in Geel, Belgie! (3 ploegen V/L/N 27% premie)
De Geel site is de enige vestiging in het wereldwijde J&J netwerk die een Lanceer- en Groei opdracht heeft, wat maakt dat er boeiende nieuwe producten en technologieën elke dag op de agenda staan.
Bij J&J speelt elke collega een vitale rol en zijn er trots op dat ze het verschil maken voor de wereldwijde volksgezondheid.
Zelf krijgen ze daarbij de kans om initiatief te nemen en hun vaardigheden te ontplooien.
U bent verantwoordelijk voor:
* Bedienen en reinigen van apparatuur (voor breken, malen, zeven, homogeniseren en afvullen) volgens de geldende werkmethodes en procedures, teneinde de poeders correct fysisch te bewerken tot de gewenste korrelgrootte.
* Correct demonteren en monteren (precisiemontages) van apparatuur volgens de geldende werkmethodes en procedures.
* Zorgen voor veiligheid, kwaliteit en milieu op de werkplek en de nodige acties nemen bij onveilige situaties.
* Toepassen van alle procedures inzake regelgeving en controles (bvb.
werken met actieve stoffen, werken met narcotica, …).
Kwalificaties/Vereisten:
* Je hebt een A2 diploma in een technische richting of bent gelijkwaardig door ervaring.
Technisch inzicht, logisch redeneren en continu verbeteren is jouw ding.
Ervaring in chemische of farmaceutische sector en kennis van het werken onder GMP-richtlijnen is een pluspunt
* Je bent een echte teamspeler en communiceert helder, oprecht en respectvol met je collega’s en leidinggevende. Je bent iemand die veiligheid en kwaliteit bovenaan zet.
Je kan nauwkeurig werken volgens GMP met oog voor detail.
* Je bezit de basisvaardigheden om met een computer te werken en kan werken met digitale toepassingen.
* Volledige beheersing van de Nederlandse taal vereist.
Deze functie start met twee opeenvolgende contracten van 6 maanden.
Bij goed functioneren volgt daarna mogelijk een vast dienstverband.
We kijken uit naar uw kandidatuur!
#RPOAMS
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Type: Permanent Location: Geel, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-14 08:00:20
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Marketing
Job Sub Function:
Product Management
Job Category:
Professional
All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Warsaw, Indiana, United States of America
Job Description:
Johnson & Johnson MedTech, we are searching for the best talent for a Marketing Manager, Global Growth Marketing Knees to be in the Palm Beach Gardens, Florida or Warsaw, Indiana.
About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
The Marketing Manager will be responsible for the formulation and execution of global marketing strategies contributing to the profitability and market penetration of Johnson & Johnson MedTech Knee Products.
The Marketing Manager will be focused on downstream marketing for the Primary Knee portfolio.
You will be responsible for:
* Commercial leadership within the Knee business.
* Firm understanding of market needs.
* Aligning customer insights with product capabilities and messaging.
* Collaborate with internal and external partners to ensure alignment between demand and supply.
* Extend a high performing culture that encourages collaboration and inclusiveness within the team, and across stakeholder groups.
Commercial Results
* Achieve business plan objectives of sales, net income, gross profit, inventory and price on an annual basis.
* Manage expenses within budget.
* Increase company’s leadership position in the Knee market.
Product Launches
* Responsible for leading and executing impactful product launches.
* Specific responsibilities include the development of the brand strategy, marketing materials for all key customer groups, pricing strategy, promotional plans, product training plans (sale...
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Type: Permanent Location: Palm Beach Gardens, US-FL
Salary / Rate: Not Specified
Posted: 2025-07-14 08:00:08
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Automation Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Cornelia, Georgia, United States of America
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for Automation Engineer II to be in Cornelia, GA.
The Automation Engineer II is responsible for leading or supporting design, installation, and qualification of new manufacturing equipment and improvement/optimization of existing manufacturing equipment.
The engineer in this role will also provide technical expertise to resolve manufacturing equipment and automation issues.
The role of Automation Engineer II will support Suture Materials Manufacturing in the Ethicon MedTech manufacturing facility in Cornelia, Georgia.
Key Responsibilities:
* Collaborates with other plant functions and external vendors to support design of new manufacturing equipment or modify existing manufacturing equipment in accordance with regulatory, industry, and J&J standards.
* Effectively and safely manages or supports projects to meet business objectives, including quality, financial, EH&S, and performance goals.
* Supports qualification coordination and execution of new and/or improved manufacturing equipment and automation systems.
* Leads or supports quality and safety investigations related to equipment.
Achieves timely closure of corrective actions.
* Supports evaluations of new technologies to improve process safety, quality, reliability, and efficiency.
* Prepares oral and written technical reports and project updates
* Coordinates training of personnel on equipment operation and maintenance
* Analyzes maintenance trends in area of responsibility to support asset investment strategy
* Organizes and presents Capital Appropriation Requests (CAR) for project scope and funding.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
* Adheres to J...
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Type: Permanent Location: Cornelia, US-GA
Salary / Rate: Not Specified
Posted: 2025-07-14 08:00:06
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Anasco, Puerto Rico, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Finance Coop to be in Anasco, PR.
* The typical Co-op term is from August, 2025 to August, 2026
* Full time requirement (40 hours per week)
Purpose:
Students with interest in the areas of finance and accounting on a medical device manufacturing environment can gain broad exposure to our processes in J&J Surgical Vision.
Our Coop Roles encourage college students to explore their professional interests while working on real business projects.
Our goal is to bring Accounting students topics to their professional life.
Providing an opportunity to see what job opportunities are possible, have on hands experience and prepare each student for a potential full-time position after graduation into one of our challenging leadership programs or direct hire roles.
Experienced leaders mentor student contributions and support their technical and professional development during coop/internships.
In addition to valuable work experience, students can also have the opportunity to build leadership and functional skills through leadership exposure, on the job training, presentation skills, communicating in the workplace at different levels and other enriching topics.
You will be responsible for:
Supports accounting tasks such as:
* Capital appropriation requests
* Project expenses monitoring
* Business Partnering
* Cost improvement projects monitoring
* Month c...
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Type: Permanent Location: Anasco, US-PR
Salary / Rate: Not Specified
Posted: 2025-07-14 08:00:00
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for an Associate Scientist, Cell Line Development to be located in Spring House, PA.
Purpose: The Therapeutics Development & Supply department of Johnson & Johnson Innovative Medicine is seeking an ambitious Associate Scientist to join the Cell Engineering and Analytical Sciences (CEAS) group located in Spring House, PA.
Our group specifically generates cell lines that produce large molecule therapeutics in support of the fast-growing pipeline for various therapeutic areas.
You will be responsible for:
* Developing mammalian cell lines secreting complex proteins, including transfection, clone characterization, and bioreactor evaluation.
* Evaluating and implementing cutting-edge technologies in cell biology, molecular biology, genome editing, or equipment to improve protein yields and shorten timelines.
* Employing cell & molecular biology techniques such as nucleic acid manipulation, ddPCR, Western blotting, and gene editing technologies for production of high-quality manufacturing cell lines for complex biologics.
* Interacting with peers from specialty areas and developing scientific expertise.
* Working independently to design experiments, analyze data, troubleshoot, and maintain detailed records for laboratory notebooks and other technical documents.
Qualifications / Requirements:
Education:
* A minimum of a Bachelor's degree in Biological Sciences, Biochemistry, Chemical Engineering or a related scientific field is required.
An advanced degree (Master's) is preferred.
Experience & Skills:
* A minimum of 1 year of relevant research experience in one of the following areas: protein expression, cell cultu...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:59
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Assembly
Job Category:
Non-Standard
All Job Posting Locations:
Limerick, Ireland
Job Description:
We are searching for the best talent for the Production Technician role to be in Limerick, Ireland.
About MedTech:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
As a Production Technician, you will:
* Update supervisor of work status or problems with recommendations for improvement or correction
* Assist in modifying procedures to improve equipment operation or processes
* Respond to basic system alarms and reset alarms as necessary
* Record assignments and prepare documentation concerning materials, parts used, concepts, designs, drawings, and processes
* Conduct testing protocols and document results
* Implement manufacturing phase-in of new products or product changes
* Identify safety issues and provide support in their resolution
* Participate in specialized studies or experiments as needed
Required Qualifications:
* A Leaving certificate or equivalent certificate
* Minimum 2 years’ experience in a production technician role or similar
* Experience working in the medical device environment (Pneumatic systems, PLCs, Machine Automation, Equipment Set up, Pick and Place Machinery)
Preferred Qualifications:
* Previous relevant experience in a production environment
* Ability to work on own initiative
* Attention to detail and flexible work ethic
* Training and experience in Packaging/print equipment, High volume manufacturing, Mechanical setup, Injection moulding, Electromechanical)
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs.
If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
Note:
Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description. QUMAS procedures will define responsibil...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:54
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Testing Coordinator to be based in Leiden, Netherlands.
“Caring for the world… one person at a time” inspires and unites the people of Johnson & Johnson.
We embrace research and science—bringing innovative ideas, products, and services to advance the health and well-being of people.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
This culture of caring is the focus of our corporate philosophy, anchored in the internationally applicable Credo.
You will be responsible for:
* Leading the coordination of all raw materials testing, ensuring on-time completion in line with production needs.
* Facilitating daily meetings with stakeholders to align processes and ensure seamless execution of testing activities.
* Reporting on project status and escalating any changes or constraints to the management team in a timely manner.
* Managing deviations in raw material testing, conducting investigations, and implementing corrective and preventive measures.
Qualifications/Requirements:
* A Bachelor’s degree (or equivalent) in a relevant field along with 2-5 years of experience in quality control and raw materials testing.
* In-depth knowledge of Good Manufacturing Practices (GMP) and proven experience in quality control environments.
* Strong verbal and written communication skills in English, with the ability to engage effectively with a diverse range of stakeholders.
* Proficient in eLIMS, SAP, and Excel for accurate data analysis, with a strong ability to adapt to shifting testing timelines and effectively prioritize urgent requests.
This is your opportunity to bring your expertise to a dynamic environment where innova...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:53
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Supplier Quality
Job Category:
Professional
All Job Posting Locations:
Shanghai, China
Job Description:
* In accordance with all applicable federal, state, and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Provide timely business support for the assigned Ethicon Source Quality Management (SQM) function globally.
* Lead, develop, and implement supplier/purchasing controls and associated activities including Approved Supplier List management.
* Participate in and/or lead the identification, selection, qualification, monitoring, and disengagement of suppliers for Source Quality Management.
* Collaborate with suppliers and business partners to ensure robust materials, products, processes, and systems.
* Partner with Procurement, R&D, Engineering/Technical Operations, Quality, Operations, and Suppliers in the timely investigation, resolution/prevention of supplier-related issues to minimize/prevent business disruptions.
* Monitor and analyze supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes.
* Implement supplier change management process including change notification, dissemination of information, impact assessment, approval of changes, and supports material/supplier qualifications.
* Own, drive, and lead the assigned Supplier Quality related projects, activities, initiatives with limited supervision.
* Utilize Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for SQM projects.
* Utilize analytical and problem-solving skills to develop and optimize supplier performance.
* Analyze quality data and identify trends impacting risk benefits requirements of product and quality systems for external suppliers.
Lead discussions to drive resolution.
* Collaborate with operations and franchise operations development on process/product improvement projects.
* Prepare Supplier Quality Agreements and drives discussion with supplier while consulting Source Quality Manager.
* Develop/execute Quality Risk Management process for supplier-related matters with partnerships of subject-matter experts.
* Own and lead the Source Quality Relationship Management (SQRM) process for the assigned suppliers (e.g.
L...
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:41
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Product Development
Job Sub Function:
R&D Mechanical Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Aachen, North Rhine-Westphalia, Germany
Job Description:
The Sr.
R&D Mechanical Engineer (m/f/d) ensures that relevant job related quality procedures are followed at all times.
Tasks and Responsibilities:
* On time CAD-modeling and designing of pump prototypes, parts fixtures and assemblies incl.
related shape and position tolerances
* Investigation into interferences of shape and position tolerances
* Comparison of real parts with CAD geometries and specifications
* Assistance for testing new parts with regards to fulfilling their specifications
* Documentation of parts, sub-assemblies, fixtures according to the needs of the quality system
* Identification of Drawings/Documentation improvement requirements
* Strong collaboration with simulation team with regards to design optimizations
* Providing and storing of test/measurement reports according to Abiomed-J&J standards and requirements
* CAD-modeling and drawing in Solid-Works: parts, sub-assemblies, fixtures
* Assistance in supplier qualification
* Assistance in introducing new parts (specification of critical dimensions, first article specs and investigation)
* Interface for supplier communication and alignment with regards to new designs
*
Education: Bachelor’s or master’s degree in Mechanical Engineering, Medical Engineering or alike or a qualification with comparable skills in combination with >5y work experience;
Working Experience:
* Senior Work Experience in 3D-CAD (Proven Works) including modelling, structuring of parts and assemblies, drawing extraction and data management in Proven Works EPDM
* Advanced knowledge of tolerances and fits including shape and position tolerances, as well as surface definitions (roughness & waviness) and related measurement technology
* Outstanding understanding of 3D-geometries
* Proficient in German and English language
* Hands on mentality;
* Experience in mechanical manufacturing (lathing, milling, drilling, grinding, tumbling, etc.)
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:36
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Automation Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
US014 MA Raynham - 325 Paramount Dr, US161 IN Warsaw - 700 Orthopaedic Dr
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Johnson and Johnson is recruiting for a Manufacturing Systems – BPO to be located in Warsaw, IN or Raynham, MA.
Johnson & Johnson Medtech is a leader in orthopedics, providing one of the most comprehensive portfolios in the industry.
Our Joints reconstruction manufacturing facilities are located globally, including sites in Raynham & Bridgewater, MA; Warsaw, IN; Cork, Ireland; Blackpool, UK; Leeds, UK; Suzhou, China; and a new site in Costa Rica.
Position Summary :
Reporting to the Joints Global Manufacturing Systems Standards lead, the MES/Low Code Business Product Owner will be responsible for the development, implementation, and maintenance of manufacturing systems and data, such as manufacturing execution systems (MES) and low-code development platforms.
This role will act as the liaison between business stakeholders (e.g.
Operations, Quality and Engineering) and the global product teams to ensure alignment with business objectives and drive innovative solutions.
Key Responsibilities :
• Product Vision: Define and communicate the product vision, strategy, and roadmap for Manufacturing Systems such as MES and low-code applications.
• Stakeholder Engagement: Collaborate with business stakeholders to gather requirements and translate them into functional specifications.
• Feature Prioritization: Working with the global product teams, prioritize product features and enhancements based on business impact, user feedback, and strategic alignment.
• Development Oversight: Work closely with development teams to ensure timely delivery of high-quality features.
• User Acceptance Testing: Faci...
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Type: Permanent Location: Warsaw, US-IN
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:29
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Ciudad Juarez, Chihuahua, Mexico, MX301 – Circuito Interior Norte - BWI
Job Description:
Purpose:
Under general supervision, participate in new and sustaining product/process teams to develop quality-engineered systems and products, lead and support design verification tests, process validations, quality processes to ensure compliance with the company’s Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO 13485, CMDCAS, PMDA and other worldwide regulatory agencies, Johnson & Johnson Environmental, Health & Safety Practices, and other applicable standards as pertains to medical devices.
Supports quality assurance activities intended to ensure effective product quality processes are in place and executed throughout lifecycle of product.
Will receive technical guidance on complex problems, but independently develops approaches and solutions.
Work is usually well defined and is checked for progress and reviewed for accuracy upon completion.
You will be responsible for:
In accordance with all applicable federal, state and local laws/regulations and Corporate
Johnson & Johnson, procedures and guidelines, this position:
* Primary responsibilities include assisting in a supporting role on new product development, sustaining and supply chain quality projects.
Assist in the development of effective quality control and associated risk management plans.
* Write process and product validation protocols and reports, equipment qualifications, engineering change orders.
* Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE).
* Help to ensure that development activities follow design control requirements, product is tested per applicable standards, European Essential Requirements are met per the MDR, and product is properly transferred to manufacturing.
* Provide support in quality improvement opportunities as appropriate to legacy products, continuous improvement, and customer satisfaction
* Assist in planning necessary to ensure effective product acceptance.
This includes, but is not limited to, inspection instructions, equipment and gage requirements, and sampling plans.
* Support vendor audits as technical lead as needed and support Supplier Quality...
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Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:26
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Assembly
Job Category:
Business Enablement/Support
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for CAR-T Manufacturing Operator to be in Raritan, NJ.
Purpose: This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment.
This position is responsible for quality and maintaining the highest standards in compliance with company policies, procedures, and all applicable regulations.
Responsible for fostering site pride and J&J citizenship.
You will be responsible for:
•Be part of the manufacturing operations team responsible for the production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.
•Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.
•Execute manufacturing activities common to cell culturing, purification, aseptic processing, and cryopreservation using appropriate techniques.
•Perform process unit operations according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP).
•Work in a team-based, cross-functional environment to complete production tasks required by shift schedule.
•Aid in the development of manufacturing processes including appropriate documentation.
•Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members.
•Handle human-derived materials in containment areas.
•Support schedule adjustments to meet production.
•Accurately complete documentation in SOP’s, logbooks, and other GMP documents.
•Demonstrate training progression throu...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-14 07:59:26
