-
Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!t
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire an Analytical Sciences Specialist to join our Analytical Sciences team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Analytical Sciences Specialist is responsible for supporting projects by developing and maintaining documentation and tasks required to fulfill project needs as well as auditing.
This Specialist will work alongside Analytical Scientists to drive activities, accelerate timelines, offer ideas to implement future enhancements and efficiencies, and provide adequate quality oversight and expertise for the creation and review of internal quality documents.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
Lab Project Coordination
* Coordinate with the team across multiple projects to ensure that the timelines are met by communicating milestones and other deadlines within the projects.
* Implement procedural changes to existing internal systems to gain efficiencies to get products to clinical trial status earlier by working with Quality Assurance as well as other departments to implement change (i.e., participates in continuous improvement activities within the group).
Data Auditing Support
* Audit laboratory data for correctness, completeness, and compliance with cGMPs and the company’s internal quality standards (i.e., auditing laboratory data for early through late phase CTM and Registration batches).
* As part of the stability program, audit laboratory stability data and coordinate with the Stability Department to manage the stability testing schedule.
* Follow-up with Quality Assurance and Analytical Sciences staff to facilitate any corrections to data as required.
Lab Compliance Support
* Contribute to the creation and/or review of Quality and Regulatory documents, as needed.
* Managing the action items assigned to the group in various compliance documents (e.g., Change Controls, CAPAs, and Investigations). These ac...
....Read more...
Type: Permanent Location: Vandalia, US-OH
Salary / Rate: 76500
Posted: 2025-09-10 08:25:22
-
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:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
Johnson & Johnson is currently recruiting for a Data Analyst Intern, from January to early May 2026, located in Manila, Philippines.
The Data Transformation & Business Intelligence team within Data & Artificial Intelligence (Data & AI) provides delivery of Data transformation tools, process, management, and creation of different business intelligent tools & automation processing tools across Global Services.
The intern will be responsible to create and help the team improves data process documentation that includes, data elements identification, lineage, usage/consumption as well as the different tools and its usage.
The intern will also assist with the successful creation and delivery of a single tool to be used to onboard newbies of the team.
The intern will be engaging continuously with other Visualization Analyst, Reporting and Analytics team, Data Scientist and Data Engineers across the organization to execute on the different requirements and will ensure efficient data delivery design documentation and process flow consistent throughout ongoing projects.
Major Duties & Responsibilities
* Develop a tool to be used to onboard newbies of the team
* Document data process, data elements, data collection process, transformation logics and usages into different business intelligence tools
* Ensures standards and outstanding practices are established and met for consistent and accurate use.
* Work closely with data and analytics specialists to strive for greater functionality in our data systems.
* Contribute creative and innovative ideas to the team
* Perform other work-related duties as assigned.
Qualifications
* Currently pursuing a degree in the field of Data Science, Data Management, Computer Information Technology, Statistics, or any related field
* Knowledge in Tableau, PowerBI or any related visualization tool.
As well as knowledge on data management is an advantage.
With familiarity of databases like Alteryx, Google, Domino, Databricks, VBA, SQL, and similar tool sets
* Excellent communication skills in English – written and verbal
* Proactive, results-driven, and detail oriented
* Strong analytical...
....Read more...
Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-09-10 08:23:12
-
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:
Market Access
Job Sub Function:
Reimbursement
Job Category:
People Leader
All Job Posting Locations:
Cleveland, Ohio, United States, Michigan (Any City)
Job Description:
We are searching for the best talent for a Therapy Access Manager in our Cleveland, OH territory.
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
Johnson & Johnson Innovative Medicine’s Patient Engagement and Customer Solutions (PECS) team is recruiting for a Therapy Access Manager which will be a field-based position.
PECS is committed to setting the standard on Patient Experience (Px), building more personalized, seamless, and supportive experiences to help patients start and stay on treatments across the portfolio.
An important aspect of patient unmet need includes helping them start and stay on their medicine for the best chance at treatment success.
The Patient Engagement and Customer Solutions (PECS) organization serves patients, during their treatment journey with Janssen therapies, to help overcome challenges to fulfillment, on-boarding, and adherence.
The Therapy Access Manager (TAM) is responsible for serving as the primary field-based lead for education, assistance, and issue resolution with healthcare providers (HCPs), and their office staff, with respect to patient access to J&J Pulmonary Hypertension therapies. This role involves investing time (up to 75%) on-site with HCPs, assessing their education needs and facilitating collaboration with various stakeholders.
A Day in the Life
Every patient’s healthcare experience is unique - shaped by personal experiences and beliefs, the presence or absence of support networks, provider and payer dynamics, and socioeconomic factors.
For many patients, the decision to start or stop a treatment is overwhelming.
J&J recognizes this, and wants to create an experience that is personalized, helpful, and hopeful.
Primary Responsibilities:
Primary responsibilities include the following.
Other duties may be assigned.
* Equip HCPs and their staff, through education, ...
....Read more...
Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:36
-
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:
Product Safety
Job Sub Function:
Product Safety Risk Management
Job Category:
Scientific/Technology
All Job Posting Locations:
Horsham, Pennsylvania, 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/.
Johnson & Johnson Innovative Medicine is recruiting for a Global Safety Strategy & Risk Management (GSSRM) Pharm.D.
Fellow, located in Horsham, PA.
The GSSRM Pharm.D.
Fellowship is a postgraduate training program designed to prepare the Fellow to become proficient at safety analyses and ad hoc report writing.
The Fellow, in partnership with the Medical Safety Officer (MSO) and under the mentorship and support from the preceptor, is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
The Fellow will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.
The Fellow will gain a high-level understanding of case processing, safety surveillance, and review of medical literature and clinical trial data.
The Fellow will function under the guidance/support from the preceptor, and other team members, be able to link discussions to content, and deliver quality results with guidance from the preceptor and the team.
Key Responsibilities:
* Support safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.
* With mentorship from the preceptor and/or Safety Anal...
....Read more...
Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:34
-
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 Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
A Lead, Local Trial Manager is considered as a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
This role is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
The Lead, Local Trial Manager is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents.
The Lead, Local Trial Manager is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
The Lead, Local Trial Manager actively leads or contributes to process improvement; training and mentoring of other LTMs and Site Managers (SM).
Compared to Associate, Local Trial Manager and Senior, Local Trial Manager roles, a Lead, Local Trial Manager is often assigned to more complex protocols and can work across Phase 1 – 3 studies in multiple therapeutic areas as needed to drive business needs.
The Lead, Local Trial Manager may also perform the role of Trial Delivery Manager (TDM)/Trial Delivery Leader (TDL) for single country as described in GCO procedural documents.
Principal Responsibilities:
1 May be delegated by Functional Manager (FM)/Clinical Research Manager (CRM) to lead country protocol feasibility (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and TDM/TDL.
Implements any local criteria for site selection.
Ensure consistent conduct of Site Qualification Visits and instruct teams on appropriate follow-up of Site Qualification Visit report and country feasibility report.
Recommends suitable sites for selection to participate in trial.
2 Collaborates with the Program Delivery Leader (PDL), TDM/TDL, local management/Country Head and other study team member to select final site list.
3 Contributes input to the study management documents at a country level or initiates development o...
....Read more...
Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:33
-
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:
Project/Program Management Group
Job Sub Function:
Project/Program Management
Job Category:
People Leader
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Raritan, New Jersey, United States of America
Job Description:
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
Johnson & Johnson MedTech Customer Engagement Platform Team is recruiting a Sr.
Manager, MedTech Global Business Product Owner (Duration role- 2 years).
The Business Product Owner in partnership with key business stakeholders and alignment with leadership will drive innovative strategic business solutions.
The Business Product Owner will focus on leading and successfully executing CRM, Pricing & Contracting, Order Management & several other capability offerings.
This BPO is responsible for the success and sustainability of multiple product capabilities and for building strong partnership and collaboration with various teams to address business needs and long-term strategies.
Responsibilities:
Under limited supervision and general direction, and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines, this position with work in the following primary areas:
* Ownership of product solution success, ensuring product investments are secured & deliver value throughout product lifecycle.
* Understand the business impact of different solutions and the ability to assess the tradeoffs between business needs, technology requirements, and costs.
* Collaborate with leaders and team members to ensure successful market launch and continuous improvement across the product lifecycle.
* Demonstrate and understand critical project and program management considerations.
* Possess a detailed understanding of business processes and data within and across areas.
* Provide project/process reviews and implement enhancements based on feedback from business stakeholders.
* Demonstrate experience working with internal and external customers in a coordinating role and gathering requirements and needs based assessments.
* Analyze the business value of potential process changes, identify, define, and...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:29
-
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:
Supply Chain Manufacturing
Job Sub Function:
Plant Management
Job Category:
People Leader
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 a Manager, Cryopreservation Operations Growth & Partnerships to join our Team in Raritan, NJ.
Summary:
The Cryo Ops Growth and Partnership Manager will be responsible for base business supply of commercial cryopreserved starting material for CAR-T, Advanced Therapies.
The role manages cryopreservation centers (CPCs) to ensure that starting apheresis material meets customer needs, provides the highest quality at the lowest total cost of ownership, and achieve maximum relationship value through accelerated innovation, supplier integration, process improvements, and collaboration.
The external require extensive interaction with key business functions, critical supplier leadership, and other segment/functional leadership.
The role acts as Virtual GM for assigned relationships, providing oversight for all activities and leads Virtual Management teams (VMTs) including Quality, Technical, Procurement, Planning and Finance to drive high performing sites.
The role will shape external cryopreservation network strategy to drive innovative solutions that allow for growth and scale.
Key Responsibilities
* Deeply understand and communicate evolving market opportunities.
* Lead partner assessment and new product implementation in coordination with cross-functional partners (MSAT, Quality, Planning, etc.), including site visits.
* Define tech transfer expectations and supply strategy with partners.
* Serve Virtual General Managers with external partners and lead JNJ team in partner management, providing oversight of all activities and financials.
* Establish and maintain performance metrics and targets with the goal of improving supply, processes, and systems
* Partner with procurement in agreement negotiations and ensure prope...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:27
-
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:
Technology Product & Platform Management
Job Sub Function:
Technology Operations Support
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Latina, Italy
Job Description:
Job Description:
J&J Innovative Medicines is recruiting a Formulation Scientist.
MSAT Small Molecule Drug Product is accountable for capturing and intensifying the scientific cornerstones for our innovative formulations and leading productivity, compliance, and sustainability throughout their commercial lifecycle.
You will be responsible for scientific assessment and optimization of formulation & process robustness, enhance product quality, and ensure regulatory compliance in the domain of liquid and/or solid dosage forms.
The ideal candidate will have a strong background in pharmaceutical development and tech transfer with a passion for innovation and problem-solving.
Responsibilities
* Provide technical support for technical transfer, PPQ, and commercial manufacturing operations, including sensitivity analysis, root cause analysis, and impact assessments.
* Plan, design, execute, and document lab and plant studies related to formulation, and process optimization in support of commercialization and lifecycle management.
* Write, review, and approve protocols, reports, and regulatory submissions, and monitor market trends, competitive landscapes, and emerging regulations to inform strategic decision-making.
* Provide subject matter expertise (SME) to prepare and support technical project reviews and operational excellence initiatives, and support or lead initiatives for compliance, resilience, formulation and process robustness optimization.
* Collaborate with expert communities in development and supply chain to establish, maintain, and deploy best practices for formulation and process development and intensification, advancing the scientific foundations in Supply Chain.
* Leverage networking and influencing skills to ensure effective collaboration with partners in R&D and Supply Chain, and prepare and review relevant technical documents, such as risk assessments, change controls, regulatory submissions, deviations, validations, protocols, procedures, ...
Requirements
* Advanced degree in Pharmaceutics, Biotechnology, Engineering, Physics, or related area
* Min 3 years of experience in development and tech transfer of solid dosage forms
...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:25
-
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:
Medical Affairs Group
Job Sub Function:
Medical Writing
Job Category:
People Leader
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicines is recruiting for an Associate Director, Medical Information Scientific Engagement (MISE) located in Titusville, NJ.
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
The Associate Director, Medical Information Scientific Engagement (MISE) is responsible for leading a team of highly skilled healthcare professionals who are experts in providing accurate, timely, balanced and up-to-date medical and scientific information to healthcare professionals (HCPs), patients, and healthcare decision makers across all Johnson & Johnson Innovative Medicine (JJIM) products and therapeutic areas within Scientific Affairs.
This individual is responsible for the organizational effectiveness, management and continuous optimization of the customer experience and engagement strategies within given therapeutic areas.
The Associate Director will lead and foster a culture of customer excellence, innovation, accountability and high performance.
This customer and compliance focused position ensures excellence in customer experience, management of service levels, handling of product events, continuous business processes, uninterrupted provision of services across omni-channel access to medical information support and accurate review of scientific responses.
This individual is responsible for the development of all direct reports by supporting the development of Human Resources Planning (HRP) programs including management development and training to meet current and future business needs while providing an environment which encourages, values, and lives the company’s commitment to equal employment and diversity, equity, and inclusion (DE&I).
Key Responsibilities:
* Provide manager review for, but not limited to, patient scientific responses and US escalation one-off responses for medical accuracy, fair balance and co...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:24
-
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:
Jacksonville, Florida, United States of America
Job Description:
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 looking for the best talent in Materials Engineering.
Materials Engineering CO-OP helps deliver a wide range of raw material characterization and qualification projects by performing a variety of engineering and research assignments.
Additionally, the CO-OP will have the opportunity to work with Global Material Suppliers and Teams both domestically and internationally.
You will be responsible for:
* The CO-OP reviews the progress and evaluates the data and presents the results of multiple projects across various functional groups.
* The CO-OP coordinates raw material and contact lens testing and protocol requirements as necessary to achieve project completion.
* The CO-OP facilitates and conducts engineering assignments involving business continuity and cost improvement projects.
* The CO-OP acts as an advocate for the continuous improvement of technology and processes.
* The CO-OP adheres to environmental policy and procedures and supports department environmental objectives.
* The position gives students multiple opportunities to work with both internal multi-functional teams as well as interact with the external partners and raw material suppliers.
Qualifications:
* Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.
* Currently pursuing a University degree, completing minimum undergraduate sophomore year prior to internship or co-op start date.
* Availability to work on site if the position requires it.
* Availability to work full time (40 h/w) for the entire co-op or internship.
* Having a graduation date after the contrac...
....Read more...
Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:11
-
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, Mexico
Job Description:
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 Quality Engineer to be in Juarez City.
You will be responsible for:
* Revision / analysis of the effectiveness of problem resolution techniques such as (PCDA), Six Sigma, Kaizen, Lean Techniques and other tools and improvement programs.
* Compliance / Regulatory
* Revises / analyzes if the current products and processes (including taken actions or decisions) comply with the regulations, such as QSRs, ISO 13485, etc.
including providing support during scheduled internal and external audits.
* Participates in quality readiness and in activities for/or interactions with regulatory agencies (FDA, JJRC, BSI, etc.).
* Responds to internal or external audit observations related to the function of quality engineering.
* Establishes and properly maintains the required documentation of quality engineering activities and/or quality systems.
* Performs periodical audits of the line to evaluate GMPs, production controls, lot segregation and process audit according to JJPS.
Checks the audits results of the area ton ensure that the corrective and preventive actions are adequate
* approves, executes IQ, OQ, PQ, TMV or Software Validation.
* Maintains and periodically revises the CTQs in the manufacturing process to guarantee the continuous satisfaction of the customer.
* Provides support in the revision and maintenance of PEMEAs, Quality control plans, process instructions and additional manufacturing documents.
* Develops, interprets and properly implements process monitoring and control methods consistent with the process/product risk level.
* Evaluates and interprets common variation causes vs special in the manufacturing process and determine the adequacy of the current process limits.
* Evaluates the needs of risk mitigation techniques given the classification of the product, potential types of defects, defect frequency, severity, risk to the patient, process capacity, process control, etc.
...
....Read more...
Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-09-10 08:22:06
-
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:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for Principal Scientist, Biostatistician to be in Spring House, PA.
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
Purpose:
The Principal Scientist, Biostatistician, has established experience working in the pharmaceutical industry, capable of independently performing and leading statistical work within a project.
This individual provides statistical support to immunology early development projects including study design, analysis planning and execution, modeling, interpretation, and communication of trial results, and is key member and statistical methodology expert in the compound team.
You will be responsible for:
The Principal Scientist, Biostatistician works as a lead statistician to provide statistical thinking and contributions to the delivery of studies, development plans, regulatory strategy, high-quality decision support to enable informed compound development decision making.
This individual is accountable for execution of individual project responsibilities, including meetings with necessary project team members, reporting activities, data analyses, and support publications for individual clinical trials/projects.
In addition, s/he investigates and applies novel statistical approaches for relevant statistical issues including modeling and simulation; contribute to or lead the improvement of processes, standards and best practices within the statistical department; and interact with external scientists and represent J&J via publications and presentations on novel statistical approaches and best practices.
Qualifications / Requirements:
* PhD in Statistics with a minimum of 2 years relevant experience or Master’s in Statistics with commensurate years of relevant experience
* Proficiency in SAS or R or other relevant computational tools
* Excellent communication sk...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:21:50
-
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:
Biological Research
Job Category:
People Leader
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
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
Johnson & Johnson Innovative Medicine (J&J IM) is recruiting for the role of Director, In Silico Discovery, Protein Therapeutics/Computational Antibody Design within our In Silico Discovery Team. The preferred location for this position is Spring House, PA. Consideration will also be given for individuals to be located in San Diego, CA and Cambridge, MA.
We are seeking creative, self-motivated leader to join our In Silico Discovery Protein Therapeutics team.
We are expanding our AI/ML capabilities across antibody design and multifunctional molecule optimization and are seeking a visionary leader to drive this initiative.
The candidate will be a highly collaborative leader interested in impacting biologics design and development using computational techniques.
This is an exciting opportunity to join an enthusiastic, diverse, and global community of in silico scientists committed to bringing innovative new medicines to patients.
The Director will lead a core group of scientists and data scientists and will be responsible for setting and executing the strategy for internal and external innovation in evolving areas of antibody design and multifunctional molecule optimization.
This will include working with other teams within In Silico Discovery and Biologics Discovery to lead in the establishment and execution of strategic initiatives in computational design and AI/ML within this biologics space.
Significant time will be spent engaged in collaborations, change management, external engagement, and keeping in the forefront of this evolving area.
This role will report to the Senior Director of In Silico Discovery, Protein Therapeutics.
Primary Responsibilities
...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:21:42
-
Description sommaire :
En tant que gestionnaire de produit, vous définirez les exigences de notre logiciel GPRH en collaborant directement avec nos clients, et ce, afin d’assurer la satisfaction des utilisateurs.
Étant un expert du marché, vous occuperez un rôle stratégique qui nous permettra d’accroître notre position compétitive.
Dans ce rôle, vous devrez être à l’affût du marché et de son évolution en identifiant les opportunités qui répondent aux besoins des clients.
Vous êtes reconnu pour votre vision globale et stratégique, votre orientation client, votre créativité, votre capacité d’analyse, vos habiletés de communication et votre aisance à gérer les priorités? Une place au sein de notre équipe vous attend.
Description de tâches :
Ce que vous apporterez à l’équipe
* Votre rigueur à acquérir, compiler et analyser l'information du marché afin de permettre l'évolution du logiciel, et ce, en anticipant les bouleversements et en saisissant les opportunités ;
* Votre participation à la conception et l’évolution du produit en validant le besoin auprès des partenaires d’affaires et des utilisateurs finaux ;
* Votre ouverture à collaborer, conseiller et apporter le besoin fonctionnel avec nos différentes équipes de développement, de ventes et de services professionnelles ;
* Votre facilité à construire et alimenter un réseau de contact dans le domaine des affaires;
* Votre facilité à démontrer les logiciels;
* Votre implication dans la validation du produit final ainsi que dans son lancement, et ce, tout en prenant les actions nécessaires pour le bon déroulement des opérations rattachées à ce produit.
Ce qu’il vous faut
* Une expérience dans un logiciel de paie ou de ressources humaines;
* Une expérience à titre de gestionnaire de produit, formateur ou toute autre combinaison d’expérience pertinente;
* Une bonne maîtrise du français est requise;
* Une expérience dans le domaine de la santé du Québec (un atout);
* Une connaissance de base de l’anglais est requise, car nous avons des clients, des partenaires et fournisseurs anglophones, et le titulaire du poste peut avoir à l’occasion à communiquer dans cette langue.
MédiSolution, c’est aussi d’excellents avantages comme
* Des assurances collectives payées par l’employeur;
* 3 semaines de vacances payées dès la première année, une 4e semaine après 3 ans et une 5e semaine après 7 années de service dans l’entreprise;
* 5 jours de congés personnels par année;
* Un programme de REER avec participation de l’employeur;
* Un programme de reconnaissance de vie active (prime annuelle);
* Le télétravail et les horaires flexibles.
Si vous êtes convaincu d’être le collaborateur qu’on recherche et que vous souhaitez vous joindre à nous à long terme, il ne vous reste plus qu’à poser votre candidature pou...
....Read more...
Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-09-09 08:27:05
-
Lead the R&D organization for ServiceLink, a workforce management platform for utilities that is experiencing rapid growth — 36% last year and trending toward 25% in 2025.
You’ll guide a talented, motivated engineering team, set a clear product vision and roadmap, stay close to the code, and turn real customer problems into high-quality, on-time releases.
With the launch of a modern new interface in Q3 2025 and cutting-edge AI capabilities for image capture and automated form completion, ServiceLink is delivering one of the most exciting solutions in the industry.
This role combines strategic product leadership with hands-on technical depth, solution design, and close collaboration with customers — and offers the opportunity to be part of a fast-growing, innovative, and fun team.
This is a remote position open to any candidate in US or Canada.
Responsibilities:
1.
Product Vision & Strategy
* Define a 12–24 month product vision aligned to company goals and translate it into measurable quarterly roadmaps.
* Incorporate UX best practices and solution architecture principles into long-term planning.
* Own build-vs-integrate decisions and apply financial principles to R&D budget and ROI assessments.
2.
Customer & Market Discovery
* Engage frequently with utility customers and end users through interviews, betas, and discovery workshops.
* Translate customer insights into clear product requirements, specifications, and designs that balance value with feasibility.
* Partner cross-functionally with Product, Design, Sales, Support, and Partners to align delivery with market needs.
3.
Technical Leadership & Delivery Excellence
* Provide architecture direction across web, mobile, APIs, integrations, data, and security.
* Review critical designs and code, prototype solutions, and guide troubleshooting and optimization.
* Ensure predictable, high-quality delivery through strong planning, CI/CD, testing, performance, security, accessibility, and observability standards.
4.
People & Team Leadership
* Hire, coach, and develop engineers and technical leads; raise the bar on engineering and design excellence.
* Create clear career growth paths and foster a culture of engagement, accountability, and innovation.
* Lead with hands-on involvement and inspire a high-performing, motivated R&D organization.
Minimum Qualifications (Must-Haves)
* 10+ years in software development, 5+ years leading engineering teams (B2B SaaS or enterprise preferred).
* Proven hands-on skills (able to read/author production code and give concrete technical guidance).
* Architecture leadership across web, mobile, backend, integrations, and security.
* Product management experience: backlog ownership, prioritization, PRDs, data-driven decisions.
* Strong customer orientation: frequent client interaction, requirements discovery, and solution design.
* Track record of on-time ...
....Read more...
Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-09 08:27:02
-
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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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!
Your Role: Jr.
Animal Care Technician , 7am-3:30pm (rotating weekends)
The Junior Animal Care Technician is responsible for handling, restraining, feeding, and otherwise caring for Production, Quality Control, and Research animals. Must be able to perform proper documentation and proceed independently in the care and husbandry of all animals on site in accordance with Standard Operating Procedures.
Your Responsibilites:
* Preparing for incoming animals (power washing, disinfecting, facility set-up) and perform daily observation of animals, animal handling and reporting any abnormalities
* Assist in animal conditioning (vaccinations, deworming, etc.) and administer treatments prescribed by the veterinarian for livestock, companion, and laboratory animals.
* Proper operation of sterilizers, cage washers, and other equipment and proper operation of large equipment (snow removal equipment, farm machinery, fork truck, etc.)
* The ability to work in adverse outdoor conditions
* Must be able to properly document work and observations performed with strict adherence to GXP documentation
* Knowledge of proper sanitization techniques and ability to properly perform and follow rules of these techniques
What You Need to Succeed (Minimum Qualifications):
* High school diploma or equivalent
* AALAS certification at the ALAT level, or ability to obtain within 16 months of employment
* Must be able to follow verbal and written instructions and exhibit interpersonal skills that are conducive to effective communication and that contribute to a congenial teamwork environment
* The ability to work in adverse outdoor conditions
What Will Give You the Competitive Edge (Preferred Qualifications):
* Additional Education and/or Equivalent Experience
* Successful completion of National Career Readiness Work Keys assessment
* Two (2) years of related animal experience as described above
Additional Information:
* Work around high noise levels, chemicals, biological agents, and animals, requiring hearing protection...
....Read more...
Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-09-09 08:27:01
-
? À propos de CTI Santé
CTI Santé est une entreprise innovante spécialisée dans le développement et la mise en œuvre de solutions technologiques au service des professionnels de santé.
Basée à Hossegor, elle accompagne ses clients sur tout le territoire avec une approche humaine, sécurisée et performante de la donnée médicale.
La société a rejoint le Groupe HARRIS Computer en avril 2025, renforçant ainsi son positionnement et son rayonnement à l’échelle internationale.
? Vos missions
Rattaché(e) au directeur du développement, vous interviendrez sur trois grands axes :
? 1.
Gestion du parc matériel interne
* Suivi des postes en collaboration avec l'équipe Harris (ordinateurs, téléphones, accessoires)
* Accompagnement des utilisateurs internes
?️ 2.
Infrastructure et sécurité interne
* Supervision et maintenance des serveurs physiques et virtuels
* Gestion des comptes et authentification centralisée (Keycloak)
* Mise à jour des outils internes (Docker, Debian, Windows)
* Suivi des sauvegardes, journaux et sécurité
? 3.
Environnements clients
* Installation, maintenance et suppression de la solution CTI
* Communication avec les équipes techniques clients
* Mise en place des connexions aux sources de données clients
* Gestion des accès distants, licences, certificats de sécurité
?️ Environnement technique
* Jira, Jenkins, Docker, ElasticSearch (Kibana, Fleet)
* Infomaniak (DNS, e-mails, newsletters)
* Windows / Windows Server (clients), Debian / Windows (interne)
* Bitwarden, Keycloak, RabbitMQ
? Profil recherché
* Formation Bac+2/+3 en informatique ou équivalent
* Expérience d'1 à 3 ans souhaitée en gestion d’infrastructure et support technique
* Autonomie, rigueur et bonne communication
* Sensibilité à la sécurité
? Avantages proposés
* Mutuelle prise en charge à 100%
* Tickets restaurant
* Un cadeau offert pour votre anniversaire ?
* Prime vacances
* Télétravail partiel sur conditions
✅ Pourquoi rejoindre CTI Santé ?
* Une entreprise à taille humaine et en pleine croissance
* Une ambiance de travail conviviale à deux pas de l’océan
* Des valeurs fortes : engagement, innovation, proximité
....Read more...
Type: Permanent Location: Paris, FR-75
Salary / Rate: 30000
Posted: 2025-09-09 08:26:56
-
About this role: As a Clinical Manager with Fresenius Medical Care, you will ensure that quality patient care is delivered while maintaining clinical operations. As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease.
Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers.
The curriculum will cover onboarding, essential functions, leading your business, and advanced leadership. As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role.
Our culture: We believe our employees are our most important asset — we value, care about, and support our people.
We are there when you may need us most, from tuition reimbursement to support your education goals, granting scholarships to family members, delivering relief when natural disasters strike, or providing financial support when personal hardship hits, we take care of our people.
Our focus on diversity: We have built a nurturing environment that welcomes every age, race, gender, sexual orientation, background, and cultural tradition.
We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.
Our diverse workforce and culture encourage opportunity, equity, and inclusion for all, which is a tremendous asset that sets us apart.
At Fresenius Medical Care, you will truly make a difference in the lives of people living with kidney disease.
If this sounds like the career and company you have been looking for, and you want to be a vital part of the future of healthcare, apply today.
PRINCIPAL RESPONSIBILITIES AND DUTIES
CLINIC OPERATIONS:
* Manages the operations of the clinic, including costs, processes, staffing, and quality standards.
* Provides leadership, coaching, and development plans for all direct reports.
* Partners with internal Human Resources, Quality, and Technical Services departments.
* Collaborates with or functions as the Home Therapies Program Manager to oversee the facility’s Home Therapies Program.
* Maintains integrity of medical and operations records and complies with all data collections and auditing activities.
* Accountable for completion of the Annual Standing Order Review and Internal Classification of Disease (ICD) coding.
* Manages clinic financials including efficient utilization of supplies or equipment and regular profits and loss review.
* Responsible for all required network reporting and on-site state or federal surveys.
PATIENT CARE:
* Coordinates all aspects of patient care with the appropriate staff ...
....Read more...
Type: Permanent Location: Terrell, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-09 08:25:46
-
Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the field of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
....Read more...
Type: Permanent Location: Rochester Hills, US-MI
Salary / Rate: Not Specified
Posted: 2025-09-09 08:25:13
-
Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the field of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
....Read more...
Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2025-09-09 08:25:12
-
What will your job look like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position is contingent on the award of contract.
Location: Concord, NC
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or G.E.D.
* Bachelor’s Degree (or equivalent combination of education and experience) in a related field
* Minimum 5 years of transit/paratransit safety management experience
* Previous management experience in a union environment
* Thorough knowledge of all applicable safety rules, regulations – ADA, FTA and DOT to include all corporate programs
* Must possess a valid driver’s license
* Must be able to pass a pre-employment drug test and DOT physical and maintain physical throughout employment
Skill...
....Read more...
Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-09 08:23:12
-
Your Job
The Mechanical Designer will add value by performing Computer Aided Design work to assist in the development of new or existing device and dispenser products.
This position will require the ideal candidate to possess knowledge of mechanical drafting and design principles, practices, and procedures to assist the design and development of new or improved products.
Under the direction of Engineers, they will design and commercialize new products using SolidWorks 3D design software along with SAP/Engineering Control Center PLM software.
This candidate will be required to design parts produced from various manufacturing processes including plastic Injection molding.
What You Will Do
* Using 3D CAD to transform concepts, sketches, or designs from the lead engineer into designs suitable for a specific manufacturing process.
* Actively design and detail products through various stages of the development cycle.
* Integrate electrical and mechanical components including wire harnesses, wire routing, PCB footprint.
* Interact regularly and collaboratively with Electrical, Mechanical, and Project Engineering.
* Manage and create BoMs.
Organize, and maintain engineering change information within SAP.
* Willingness to take ownership, learn from your peers, be personally accountable, and offer opinions.
* Other duties in support of Product Development may be assigned as recourse needs require, such as prototype and testing.
Who You Are (Basic Qualifications)
* A.S.
in Mechanical Design, or 5 years of Design Work Experience.
* 3+ years of 3D CAD experience
* Solid Works experience desired, however experience with similar 3D modeling software considered.
What Will Put You Ahead
* Expert knowledge of SolidWorks
* Knowledge of plastic part design and injection plastic molding
* Experience using SolidWorks Electrical/schematic
* Experience in wire harness design and wire routing
* Previous role as an CAD Admin
* SAP Engineering Control Center or other PDM
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 data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating va...
....Read more...
Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-09 08:17:01
-
Your Job
Are you passionate about driving efficiency, quality, and innovation in manufacturing? We're looking for a Process Improvement Specialist who will play a critical role in enhancing operations, supporting R&D initiatives, and ensuring product quality excellence.
In this role, you'll be at the center of continuous improvement, troubleshooting production challenges, implementing cost-saving solutions, maintaining product compliance, and training plant personnel on best practices.
Partnering closely with R&D, Quality, and Operations, you'll help bring new products to market, optimize processes, and deliver lasting value for both our team and customers.
Our Team
The GP Tolleson facility employs about 115 people and serves converting customers throughout the Southwest with sustainable packaging products.
This position provides opportunities for promotion within GP Tolleson, as well as many other Georgia-Pacific and Koch facilities across the country.
Come join our team!
What You Will Do
* Serve as the onsite Process Improvement Specialist to enhance operational efficiency
* Support R&D initiatives through technology implementation, raw material qualifications, and production line enhancements
* Troubleshoot issues and develop Design of Experiments (DOE) to identify and resolve recurring manufacturing challenges
* Identify and implement cost-saving opportunities after validation
* Assist with new product development and ensure compliance through the New Substance Request (NSR) process.
* Facilitate the Change Request process by receiving requests, uploading them to the PLEX change module, monitoring approvals, and collaborating with requesters to update SOPs on SharePoint
* Update customer specifications and establish product attribute limits
* Assist the Product Quality Supervisor by:
* Maintaining accurate BOMs and Specifications in PLEX and keeping SOPs and OPLs updated in SharePoint.
* Training new plant personnel on current Product Quality procedures and updating all personnel on revised procedures.
* Collaborating with the Quality Manager to maintain training logs.
* Providing timely recommendations (Release/Scrap/Rework) for products on "Hold" using a risk management approach and entering resolutions into Plex.
* Managing lab equipment calibration and ensuring the R&D lab adheres to 6S standards.
* Supporting customer complaint resolution through collaborative root cause analysis and documenting in Plex.
* Evaluating and testing incoming raw materials for specification adherence, documenting results, and facilitating early invoice payments for contractual price discounts.
Maintain regular structured and informal communication with Product Quality Specialists, the R&D team, Quality Manager, and Operations team
Who You Are (Basic Qualifications)
* Bachelor's degree in Science of Engineering OR 4 years of work experience in a quality or process imp...
....Read more...
Type: Permanent Location: TOLLESON, US-AZ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:17:01
-
Company
Federal Reserve Bank of New York
Federal Reserve Bank of New York
Working at the Federal Reserve Bank of New York positions you at the center of the financial world with a unique perspective on national and international markets and economies.
You will work in an environment with a diverse group of experienced professionals to foster and support the safety, soundness, and vitality of our economic and financial systems.
The Bank believes in work flexibility to balance the demands of work and life while also connecting and collaborating with our colleagues in person.
Employees can expect to be in the office a couple of days per week as needed for meetings and team collaboration and should live within a commutable distance.
What we do:
Economists provide analytic support for the New York Fed's core missions and engage in scholarly research on a broad range of topics.
They contribute to the formulation and implementation of monetary policy, the supervision of financial institutions, the smooth operations of the payments system, the analysis of the impact of policies on consumers and communities and the way in which the financial system supports economic growth using insights from macroeconomics, microeconomics asset pricing and corporate finance.
Areas of research include financial intermediation, monetary policy, household and public policy and financial stability.
As an Economist, you will:
* Conduct scholarly research for publication in high-quality, peer-reviewed academic journals.
* Provide rigorous analysis of policy issues related to the Bank’s mandate using advanced modeling and econometric techniques.
* Contribute analytical work and prepare technical memoranda and briefings for senior bank leaders in support of policy decisions.
* Collaborate with subject matter experts on model development, forecasts, and analysis.
* Engage in outreach to the academic and official sector research communities through participation in seminars and conferences, as well as technical working groups.
* Perform in accord with the Bank’s touchstone behaviors, as described below.
What we are looking for:
* PhD in Economics, Finance, or a related field preferred
Please visit our website to learn more and review the FAQs prior to submitting your application.
Please indicate your area of interest in your cover letter and/or application: Fields of interest:
C – Mathematical and Quantitative Methods
D – Microeconomics
E – Macroeconomics and Monetary Economics
F – International Economics
G – Financial Economics
H – Public Economics
J – Labor and Demographic Economics
L – Industrial Organization
R – Regional, Real Estate, and Transportation Economics
Salary Range: 160,000-217,600-275,200 / year
Touchstone Behaviors set clear expectations for leading with impact at every stage of our careers and aspire to achieve in our continued growth and development.
* Communicate Authentically...
....Read more...
Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-09-08 08:13:19
-
A division of Harris, Advanced Utility Systems is looking for a Project Manager.
As a Project Manager, this professional will be responsible for managing the customer relationship during implementations and ensuring a high degree of customer satisfaction.
They will collaborate with stakeholders and internal teams to deliver projects on schedule and within the budget while meeting scope requirements.
They will possess excellent communication skills and proven problem-solving skills.
This remote role welcomes candidates anywhere in Canada.
Must be legally eligible to travel to the United States and across Canada, with the ability to commit to up to 50 percent travel based on project activities and requirements.
What your impact will be:
* Manage the scope of the project and changes to the project deliverables, while ensuring customer satisfaction and profitability.
* Explain implications of changes to project scope and priorities to client and management to ensure changes are understood and approved.
* Manage project financials.
* Proactively resolve project issues to mitigate delays and reduce the impact on project timelines.
* Provide updates to the management team and coworkers on customer/project status.
AI Augmented Project Management:
* AI supported decision making – ability to interpret AI-generated recommendations, forecasts, and risk assessments to improve project velocity, quality and outcomes.
* Prompt Engineering – craft effective prompts to elicit accurate, context aware responses from AI project management, reporting, and ticket management tools.
* Collaborative AI Tool Use – intermediate level support for Copilot for Microsoft applications and Teams to support internal and client collaboration on projects.
What we are looking for:
* Education in Business Administration or related field.
* Experience in managing software development projects through all phases of the project life cycle.
* Understanding of software development processes and methodologies.
* Ability to communicate complex technical concepts to non-technical stakeholders.
* Proven leadership abilities and experience in leading cross-functional teams.
* Excellent analytical skills to assess project progress and make data-driven decisions.
What would make you stand out:
* Previous experience in professional services as a project manager.
* PMP certification.
* Experience in the utility industry.
* Fluent in French.
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About Harris:
Harris is a leading provider of mission critical software to the public sector in North America.
As a wholly owned subsidiary of Constellation Software Inc.
(“CS...
....Read more...
Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 130000
Posted: 2025-09-08 08:11:40
