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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research – Non-MD
Job Category:
People Leader
All Job Posting Locations:
Irvine, California, United States of America, Jacksonville, Florida, United States of America
Job Description:
We are searching for the best talent to join our Vision team as a Clinical Operations Manager located in Jacksonville, FL or Irvine, CA
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 on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose:
The Clinical Operations Manager develops strategies to address complex clinical issues.
He/she manages the strategic elements of study conduct, ensuring that operating procedures and company policies are followed.
Develops and manages timelines, resourcing and budget for all JJV clinical trials.
As spokesperson and technical expert for clinical operations, provides compelling rationale for decisions and presents complex strategies in a clear message.
You will be responsible for:
* Own processes and information required to execute and support the clinical trial including clinical trial project plan, project timelines, resourcing, budget plans, and statements of work
* Accountable for the preparation and finalization of key clinical documents which include the clinical protocol, informed consent, case report form, and other essential study documents
* Manage study conduct, ensuring that operating procedures and company policies are followed and that trials meet all applicable Regulations and Guidelines required to gain approval for JJV medical devices
* Responsible for the selection of Contract Resource Organizations (CRO) and oversight of contracts, timelines, and budgets, when applicable
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-26 08:17:29
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Istanbul, Turkey
Job Description:
The Commercial Quality Intern is responsible to support daily documentation activities and quality related activities for the elements applicable to the GMP/GDP activities the LOC undertakes.
Quality Assurance
* Support Good Documentation Practices and GxP related activities
* Support for preparation, update and approve local procedures in accordance with local GMP/GDP, BQM and J&J requirements
* Support for preparation and issue process of standard forms.
* Support for filing activities.
* Support for quality compliant process
* Support for system entries and perform updates in related systems
* Support for supplier Management Activities
* Support for all QMS Activities if needed.
Compliance with Company Procedures & Ethical Principles:
* Ensures compliance with relevant agreements, legal requirements, ethical standards, Corporate Business and Security Procedures and HCBI.
* Contributes to the LOC CQ Head and RM in terms of being ready for audit.
* Fulfills confidentiality principles.
Professional & Personal Development:
* Participates in training programs and applies newly acquired knowledge and skills.
* Work towards a solution via artificial intelligence, use new platforms.
* Understanding of the definition of the term; the implications for people, processes, and technology;
* Contributes to support the digital transformation efforts of the CQ and business and essential elements of data science, science applications and innovations and supports for creation a common data science vocabulary
Experience:
* Student in Chemistry / Pharmacy / Microbiology / Medicine or a related field.
* Full competency in local languages and advance level of English
* Knowledge on MS Office applications
* Analytical Thinking skills
* Result oriented
* Job tracking
* Candidates should be under "University Student" status between June 2025 - June 2026 as the contract will be for 1-year term.
Core proficiencies required for this role:
* Organized, and able to leadwork effectively with people within a complex social, cultural, and political environment.
* Must have good communication skills.
* Must have good collaboration.
* “Hands-on” ...
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Type: Contract Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-04-26 08:17:26
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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:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Under and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Monitor all FGQA quality assurance functions.
* Establish and maintain appropriate documentation as required for Quality Assurance activities and the Quality Documentation Systems.
* Develop statistical sampling plans and perform process capability studies.
* Implement process control systems and provide technical support to process validations.
* Finish new test method protocol and report.
* Provide QS support in Product transfers and new products development.
* Assist in training new engineers, train technician and supervisors in process changes.
* Perform Complaint analysis investigation as needed.
* Participate in process/quality improvement projects.
* Support COGs initiatives.
* Responsible for following and administering safety.
* Compliance with safety policies and procedures.
* Follow J &J and Ethicon Records Management Policies for Convenience information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and the third-party vendor if applicable.
* Assist, review & approve non-conformances investigations & non-conforming product dispositions.
* Provide as needed, subject matter expert feedback on manufacturing process changes.
* Responsible for communicating business related issues or opportunities to next management level.
* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
* Performs other duties assigned as needed.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-04-26 08:17:13
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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:
Quality
Job Sub Function:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
São Paulo, Brazil
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.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
COMMERCIAL QUALITY ANALYST - Surgical Vision - Fixed Period 5 months
Johnson & Johnson Vision is recruiting for a COMMERCIAL QUALITY ANALYST - Surgical Vision, located in Embu das Artes, São Paulo, Brazil - Fixed Period 9 months.
Performs and maintains quality assurance programs, supplier systems, procedures and controls, ensuring that performance parameters of both the products and quality system elements are continually measured to drive improvement initiatives.
Provides support for quality projects.
Ensures and maintains a state of inspection readiness to Johnson & Johnson Vision business.
Key Responsibilities:
Complies with company policies, procedures, and quality standards, as well as safety and environmental regulations.
Develops solutions basic scope and intermediate complexity.
Assists in writing standard operating procedures.
Performs and provides support for the product review and release functions.
Identifies significant trends.
Generates statistical summaries.
Participates in quality system improvement initiatives.
Provides support to Supply Chain in Quality related subjects.
Assists in the documentation of corrective action plans and monitors implementation and follows up on closure of corrective and preventive actions.
Coordinates the impact assessment of the regulatory requirements applicable to Distribution Center, when defined by the Commercial Quality Leader.
Support internal and external quality audits (Corporate J&J, VISA, CRF/CRQ relate...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-04-26 08:16:24
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Cambridge, Massachusetts, 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
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
In this role, you will work with colleagues in the JNJ Innovative Medicine R&D Data Science & Digital Health organization and partner with key businesses across JNJ Innovative Medicine (formerly Janssen) to apply advanced data science and analytics to answer key research questions. As an intern, you will get the opportunity to work on cutting-edge problems at the intersection of machine learning and drug discovery.
You will be a member of a dynamic team comprising data scientists and subject matter experts to create and iterate on data science solutions.
Projects include, but are not limited to, developing, and applying predictive and generative machine learning methods for molecular property prediction with the ultimate goal of drug discovery.
Interns could be located out of Leiden office as well as remote.
Minimum qualifications:
* Currently pursuing a Masters or PhD degree in Statistics, Biostatistics, Data Science, Computer Science, Electrical Engineering, Computational Biology, Biomedical Informatics, or related quantitative discipline.
* Strong working knowledge of machine learning with demonstrated research experience, as evidenced by publications, public code contributions, or equivalent.
* Proficiency in Python and hands-on experience with Deep Learning frameworks such as PyTorch or TensorFlow to tackle scientific problems.
* Strong tech...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-04-26 08:16:17
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Ardurrra is seeking a Land Use Planner to join our team in Nampa, ID or Meridian, ID!
Job Description:
We are seeking a highly motivated and experienced Land Use Planner to join our team.
In this role, you will be responsible for developing and implementing comprehensive land-use plans and strategies that support our client’s development goals.
You will also be responsible for coordinating the development of multiple projects from start to finish, ensuring that all projects are completed on time, within budget, and to the required quality standards.
The ideal candidate will have a strong understanding of local land use regulations, local planning principles, community engagement, and a passion for creating vibrant and sustainable communities.
Required Qualifications:
* Bachelor’s Degree in Land Use Planning or similar.
* 2+ years of experience in land use planning in the private or public sector.
* A minimum of 2 years of experience in a similar role, with a strong track record of successfully coordinating the development of land development projects.
* Excellent organizational skills, with the ability to manage multiple projects and priorities effectively.
* Strong understanding of local, state, and federal land use regulations and policies.
* Excellent communication, presentation, and interpersonal skills.
* Strong interpersonal and communication skills, with the ability to effectively communicate with a wide range of stakeholders, including engineers, contractors, cities, government agencies, surveyors, attorneys, and various departments within many municipalities.
* Ability to effectively manage multiple projects and meet deadlines.
* Strong problem-solving and decision-making skills, with the ability to identify and manage project risks and issues effectively.
* Ability to work as part of a team, with project managers, engineers, surveyors and other stake holders.
Key Responsibilities:
* Conduct site analyses and research to determine the feasibility of proposed land-use projects
* Prepare and present land use applications and development proposals to clients, government agencies, and community groups.
* Route plats and other necessary project documentation.
* Participate in public meetings and community engagement events to gather feedback and build support for development projects.
* Work to ensure projects meet zoning and other regulatory requirements.
* Collaborate with other departments to ensure projects are completed on time and within budget.
* Stay current on land use planning trends, laws, and regulations.
* Attend professional development opportunities to continue expanding your knowledge and skills.
We offer a competitive compensation and benefits package, as well as opportunities for professional growth and development.
If you are passionate about land use planning and have a track record of success, we encourage you to apply.
...
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Type: Permanent Location: Meridian, US-ID
Salary / Rate: Not Specified
Posted: 2025-04-26 08:12:26
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Classification:
Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The District Manager is responsible to meet or exceed Service goals in the management of a district of routes.
Reports to the Service Manager.
A DM may manage a service center and if the service center has more than 7 routes, the DM becomes classified as a Senior DM.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Develop and motivate a district to be a highly productive team through continual training, regular meetings, daily check-in, fostering a positive work environment, route rides, and building strong relationships with each RSR.
- Ensure customer loyalty and outstanding customer service through customer visits, audits, new installs, problem solving, open communication and negotiating with customers.
- Ensure all company policies and procedures are followed in their district, including safety and Service SOP.
- Manage retention and growth by motivating their district to solicit new customers, up-sell/cross-sell/sample all lines of service or product and ensure a profitable product mix.
Monitor and report competitive activity.
Oversee promotions, contests and continued excellent customer relationships.
- Leading their district to success, communicate changes and policies, oversee route organization, project a professional image and require of their district likewise, and cooperatively work with other departments in the branch.
- Complete general route responsibilities when necessary.
Safely operate a delivery vehicle, following all applicable laws and company policy.
- Follow written and verbal instructions and perform other tasks as directed by supervision.
- A Senior DM performs the above functions as well as oversees a service center.
This includes securing the facility, managing inventory to ensure sufficient s...
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Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-25 08:35:44
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Company
Federal Reserve Bank of Dallas
We are dedicated to serving the public by promoting a strong financial system and a healthy economy for all.
These efforts take a team of dedicated individuals doing many different jobs.
Together we’re creating a workplace where talented people can thrive, and we welcome your unique background and perspective to help present the best possible solutions for our partners.
This requisition is for an Economist opening - this is a designated link for a pre-identified candidate.
Full Time / Part Time
Full time
Regular / Temporary
Regular
Job Exempt (Yes / No)
Yes
Job Category
Economics/Research Family Group
Work Shift
First (United States of America)
The Federal Reserve Banks are committed to equal employment opportunity for employees and job applicants in compliance with applicable law and to an environment where employees are valued for their differences.
Always verify and apply to jobs on Federal Reserve System Careers (https://rb.wd5.myworkdayjobs.com/FRS) or through verified Federal Reserve Bank social media channels.
Privacy Notice
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-25 08:33:48
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Who We Are:
Managed Health Care Associates, Inc.
(MHA) provides care communities access, solutions, and insights to help them run their businesses more effectively.
Our members include post-acute providers across the care continuum, including long-term care, home infusion, specialty pharmacies, senior living, and other group living facilities.
Our team of associates is passionate about our common mission of helping people age with grace and championing our core values of being Curious Learners, Selfless Advocates, and Relentless Finishers.
Who we’re looking for: (Job Summary)
The Account Executive (AE) is a results-driven sales professional who works well both in a team and independently.
The Account Executive will be responsible for managing a book of business in North Carolina & South Carolina.
The AE is responsible for establishing, developing, and maintaining positive business and customer relationships with existing accounts, as well as developing new business opportunities within the assigned territory.
The AE will offer a customized range of food service contracts, medical products, and business products contracts to Assisted Living Facilities, Skilled Nursing Facilities, Continuing Care Communities, and other types of senior care living providers.
We’re looking for a highly motivated, ambitious individual with a passion for delivering impactful solutions to clients in the senior care markets.
You’re a confident relationship-builder and skilled communicator, with a strong ability to identify and close opportunities.
You thrive in a fast-paced, self-directed environment and bring a positive, “can-do” attitude to your work every day.
What You’ll Be Doing:
In this role, you will be the face of our organization within your assigned territory.
The Account Executive will manage and grow existing client relationships while strategically developing new business opportunities.
You will collaborate cross-functionally with internal stakeholders and external partners to bring customized, cost-effective solutions to your clients.
In this role you play a key role in the customer experience—resolving issues, ensuring satisfaction, and delivering value at every touchpoint.
This is a high-impact, field-based role that requires up to 50% travel in territory.
You’ll meet regularly with clients’ key decision-makers, present data-driven insights, and offer solutions that drive compliance, savings, and long-term partnerships. Candidates for this role, have experiences working with the post-acute care market, including senior care (Assisted Living, Skilled Nursing) hospitality, and rehabilitation communities.
Sales Acumen
* Results-driven sales professional with a deep understanding of sales processes and techniques, specializing in the senior care and healthcare industries.
* Proven track record of consistently meeting and exceeding sales quotas and performance targets.
* Skilled in identifying and qualifyi...
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Type: Permanent Location: Charlotte, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-25 08:31:44
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If you are an expert EHS /Facility Supervisor looking for an opportunity to grow, Emerson, has an exciting opportunity for you! Based in Olive Branch, MS, you will be responsible for leading the Warehouse Facility and powered equipment maintenance, along with Environmental Health & Safety functions to ensure compliance with all applicable environmental, health and safety regulations, policies, & procedures.
If you love working in a fast -paced environment and you have demonstrated mechanical and electrical aptitude, this is the job for you!
Ready to make your mark and embark on an exciting journey with us? We can't wait to hear from you!
In this Role, Your Responsibilities Will Be:
EHS Job Responsibilities:
* Implement, complete, and ensure adherence to Company's Environmental Health and Safety policies and procedures
* Ensure all required company and regulatory reporting requirements are submitted timely
* Develop non-EHS site personnel to support implementation of EHS programs
* Assist in the management of workers compensation
* Collaborate with regulatory agencies (OSHA, EPA, State/Local Regulators)
* Responsible to lead management personnel in the investigations of facility incidents and complaints regarding unsafe working conditions and practices. Help identify an immediate solution, the root cause, and supervise corrective actions to completion.
* Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health, and safety policies, procedures and practices.
* Represent management during EHS Meetings along with the other facility personnel.
* Serve as a facilitator for hourly and supervisory employee EHS and New Hire training.
* Serve as an advisory Member of the Safety Committee and adhere to OSHA regulations.
* Performs other EHS duties as required by management.
Facilities Responsibilities:
* Schedule and lead preventative maintenance for all machining, assembly and other equipment located in the Olive Branch facility
* Provide maintenance support for the entire facility including management of utilities, HVAC, fire suppressant systems, etc.
* Plan and lead overall maintenance and special projects.
* Responsible for ensuring facility atmosphere,5S and hygiene compliance.
* Assist in upgrading existing equipment to safer efficient and productive alternatives.
* Establishes and maintains specific preventive maintenance schedules on equipment and facilities.
* Responsible for managing and coordinating outside vendors when onsite.
* Performs other facility duties as assigned.
WHO YOU ARE:
You build and implement plans that allocate resources precisely.
You analyze multiple and diverse sources of information to define problems accurately before moving to solutions.
You marshal resources (people, funding, material, support) to get things done.
FOR THIS ROLE, YOU WILL NEED:
* Bac...
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Type: Permanent Location: Olive Branch, US-MS
Salary / Rate: Not Specified
Posted: 2025-04-25 08:30:28
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Georgia-Pacific creates long-term value by using resources efficiently to provide innovative products and solutions that meet the needs of customers and society, while operating in a manner that is environmentally and socially responsible, and economically sound.
Headquartered in Atlanta, Georgia-Pacific LLC is one of the world's leading manufacturers and marketers of building products, consumer products, packaging, paper, cellulose and chemicals.
The company employs more than 30,000 people at approximately 300 locations in North and South America.
We are currently seeking a Product Support Specialist to join our Technical Services team.
What You Will Do
Technical Product Support:
• Provide technical support for Georgia-Pacific Building Products (gypsum, structural
panels, lumber)
• Manage inbound inquiries from both internal and external customers
• Provide timely, accurate, data-based solutions.
• Provide support to central and west coast customers
• Capture and enter accurate customer records into CRM
• Collaborate with team members and other departments for efficient issue resolution
• Cross functional collaboration across the organization
Claims Processing:
• Process product warranty claims applying critical and economic thinking
• Communicate claim status updates to customers and resolve related issues
• Track and analyze claims data to identify trends and maintain accurate records
Data Analysis:
• Analyze data and provide insights on customer trends, product trends and claim trends
Who You Are (Basic Qualifications)
• Experience using Microsoft Office Suite (e.g., Word, Outlook, PowerPoint, Excel and
Teams)
• Strong written and verbal communication skills
• 2 -3 years of related work experience
• Experience in Building Products or Construction industry
• Travel 15%
What Will Put You Ahead
• Experience with SalesForce.com
• Experience in commercial construction engineering, design, building science, consulting,
technical support, or building products.
• Claims management experience
• Data analysis skills
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
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, special...
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Type: Permanent Location: Decatur, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-25 08:25:15
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QA Auditor
Job Description
Auditor de QA
Área: Hi-tech
1er turno (Lunes a jueves diurno)
Vigencia de aplicación: 04/Mayo/2025
Su trabajo
* Es responsable de dar soporte tanto en las áreas de producción, así como recibo, el cual consiste en monitorear que el producto elaborado cumpla con los requerimientos establecidos de acuerdo con las especificaciones del producto; apoyar en los programas encaminados a mejorar los procesos y sistemas actuales como: GMP, GDP.
5’S y regulaciones aplicables, además de dar seguimiento a los procedimientos establecidos; así como el realizar actividades de inspección para la aceptación del producto.
* Promover la cultura de calidad y satisfacción del cliente (interno o externo), compradores y consumidores entre todos los colaboradores de KC para alcanzar las metas de calidad definidas.
Responsabilidad y expectativas del puesto:
* Verificar que el producto que sé está procesando cumpla con las especificaciones y los requerimientos del cliente a través de la interpretación de datos, uso de principios básicos de estadística para la toma de decisiones, mantener el estatus verde en
* EWMA/GE Plant apps durante el turno y conocimiento de planes de muestreo aplicables.
* Sugerir mejoras en el proceso para mejorar la satisfacción del cliente.
* Sugerir y verificar tanto acciones correctivas y preventivas para una mejor calidad de producto y/o proceso.
* Sugerir ideas para tener un mejor flujo de materiales.
* Documentar y seguir los procedimientos para los materiales y productos no conformes (QCHold) (Material que no cumpla con las especificaciones y que afecte directamente a la calidad del producto).
* Verificar que los misceláneos y materia prima se encuentren en buen estado, al momento de procesarlos, así como de recibir materiales, para con ello cumplan con los requerimientos establecidos para la inspección de recibo.
* Realizar un reporte diario de los problemas que se presentaron durante el turno.
* Sugerir en cuanto a la toma de decisiones con respecto a la calidad del producto (que tanto le afecta al producto en relación con el uso intencionado del mismo).
* Verifica que los componentes usados en proceso de manufactura están de acuerdo con la orden de trabajo y especificación aplicable.
* Asegura que las devoluciones de materiales y sub-ensambles que se realizan dentro de las áreas de producción se hagan de forma correcta y de acuerdo con procedimiento.
* Asegurar el cumplimiento de los requerimientos de las normas y regulaciones de calidad aplicables, de acuerdo con políticas y procedimientos ya establecidos.
* Es indispensable su presencia en el área asignada.
* En caso de ser requerido participar en la reunión de inicio de turno del área asignada (15-20 minutos) siguiendo la agenda aplicable con todos los departamentos claves, para comunicar y revisar los resultados específicos de su línea, ...
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Type: Permanent Location: Nogales, MX-SON
Salary / Rate: Not Specified
Posted: 2025-04-25 08:25:11
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
"Roche in Kürze"
Wir bringen die Wissenschaft voran, damit wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Unsere Pharma-Vision
Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele Patienten große Hoffnung und Zuversicht.
Deshalb setzen wir auf EINE Organisation und zwar #WIRGEMEINSAM in SDPM!
Verantwortlichkeiten | Das erwartet Dich
Als Facharbeiter Musterzug EMT (m/w/d) bist Du Teil des Teams Monitoring in der Abteilung Facility & Engineering Pharma.
Du bist für das chargenunabhängige Monitoring und die Durchführung von mikrobiologischen Reinraumuntersuchungen verantwortlich.
Dies beinhaltet die Koordination, Unterstützung und Verbesserung der Monitoring-Tätigkeiten im Reinraum.
Darüber hinaus übernimmst Du folgende spannende Aufgaben
● Du führst mikrobiologische Reinraumuntersuchungen durch und koordinierst den
Mustertransport in das mikrobiologische Labor.
Diese Tätigkeit erfordert das kontinuierliche Heben von Lasten bis zu 10 kg.
● Ebenso bist du für das chargenunabhängige Monitoring in Reinräumen zuständig.
Ein wichtiger Bestandteil Deiner Aufgabe besteht in der Dokumentation und Kontrolle der durchgeführten Arbeiten in Herstellprotokollen (teilweise elektronisch) und elektronischen Logbüchern
● Deine Tätigkeit setzt die Einhaltung aller relevanten GMP- und Hygienevorschriften voraus.
Im Rahmen deiner Tätigkeit stellst du die Eignung verwendeter Prüfmittel und Verbrauchs- materialien sicher
● Darüber hinaus engagierst Du dich im Rahmen unseres KVP-Prozesses zur Verbesserung
unserer Arbeitsabläufe
Qualifikationen | Das bringst Du mit
Du bist eine positiv denkende, integre und selbstreflektierende Persönlichkeit mit starken kommunikativen Fähigkeiten.
Du hast ein offenes Ohr für die täglichen Herausforderungen deiner Kolleg
*innen und schaffst ein Klima der gegenseitigen Unterstützung.
Du stellst Fragen um zu verstehen, sprichst kontroverse Themen offen und ehrlich an..
Darüber hinaus motivierst Du alle mit deiner Can-Do- Einstellung.
In diesem Sinne treibst du eine neue Denkweise und Mindset voran, die es für eine erfolgreiche Teamarbeit benötigt.
● Als Facharbeiter Musterzug EMT verfügst Du über eine Ausbildung als Pharmakant/Chemiekant/PTA/ Biologielaborant oder vergleichbare Ausbildung.
● Deine Berufserfahrung in der pharmazeutischen Produktion und idealerweise im Bereich Monitoring zeichnet Dich aus.
Darüber hinaus zeichnen Dich folgende ...
....Read more...
Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-04-25 08:11:24
-
Position Summary: The Program Coordinator for Product Development will work within the Product Development environment to coordinate accomplishment of strategic objectives and deliverables for development of new assays.
The Program Coordinator will work with PD Project Managers and Internal/External stakeholders to coordinate overarching activities associated with the development of immunoassays on automated platforms and the transfer of this technology to the manufacturing environment.
Essential Job Functions:
* Responsible for coordination, alignment, timeline management, and planning for Product Development projects.
* Collaborates with managers within Product Development, Analytical Development, Clinical Affairs, Quality/Regulatory Compliance, Logistics and Operations to meet strategic development and transfer objectives.
* Responsible for providing an environment which encourages the company's commitment to equal employment opportunity and the value of a diverse work force.
* Follows all company environmental, health and safety policies, procedures and guidelines, and conducts work in a safe manner.
* Performs other duties as assigned.
Job Specifications (skills, knowledge, special training, certification, license requirements):
* Demonstrated knowledge and experience in Project Management
* Strong leadership skills and a positive work-related attitude
* Strong communication and interpersonal skills with both technical and non-technical personnel
* Ability to supervise personnel
* Immunoassay development experience desirable
* Manufacturing and Quality Control experience desirable
* Ability to write clear, concise technical reports and attention to detail is essential
* Must be detail-oriented and thorough
* Excellent organizational skills
* Ability to work in a face-paced and dynamic environment
* Ability to work with various software packages
* Ability to make presentations to various groups of individuals
* Mastery of various project management software tools
Education and Work Experience Required:
* B.S.
/ M.S.
in Biological Sciences/Engineering, with 5-10 years of laboratory experience, preferably in the diagnostic or pharmaceutical industries
* Minimum of 3 years of project management experience
* Excellent communication and interpersonal skills, as well as demonstrated leadership ability
We offer a competitive benefits package that starts on day one, including employer-paid dental & vision, 401(k) match up to 5%, and generous PTO and holiday benefits.
We regret we are not able to respond to each resume received.
Only those selected for an interview will be contacted.
Fujirebio Diagnostics is an Equal Employment Opportunity Employer
See Job Description
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:59
-
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:
R&D Operations
Job Sub Function:
Clinical/Medical Operations
Job Category:
Professional
All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom
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/
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
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Zuchwil, Switzerland- Requisition Number - R-010890
West Chester, US – Requisition number- R-008563
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
#Li-Hybrid
#LI-RP1
The Sr.
Manager, Scientific Operations provides leadership, motivation, and strategic direction for the general technical writing activities for the generation of Clinical Evaluation Reports/Plans (CER) and Summary of Safety and Clinical Performance Reports (SSCP) for their assigned therapeutic area within J&J Global MedTech.
They also support broader initiatives and cross-platform activities to support ...
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Type: Permanent Location: Leeds, GB-LDS
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:37
-
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 Deliver
Job Sub Function:
Deliver Excellence
Job Category:
Professional
All Job Posting Locations:
Zug, Switzerland
Job Description:
Johnson & Johnson is currently recruiting for a Director, CX&S Global Process Owner to be based in Raritan, NJ, Jacksonville, FL, Mirimar, FL, Markham, CA, Sao Paulo, BR, or Zug, CH.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United States - Requisition Number: R-010404
Canada- Requisition Number: R-011032
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Job Overview:
The person will be responsible for operational excellence and an outstanding customer experience by establishing and implementing the strategy for key business imperatives, driving connectivity across the business and enabling innovation, and strong operational performance.
The GPO will lead the global development, implementation, and continuous improvement of consistent processes and standards for customer service.
This role will ensure efficiency and high-quality customer interactions across all regions.
Key Responsibilities:
Strategic Project Management:
* Provide strategic oversight and program leadership for key global initiatives to innovate and improve operations, while maintaining quality services.
* Lead teams of regional partners and collaborate to define clear global scope, priorities, timelines, and requirements as well as alignment on regional/local customization needs for customer experience and service.
* Own global communications and business partner engagement.
* Lead global design requirements to support and enable the CX&S strategy.
* Identify and partner to address project dependencies to ensure success of the collective portfolio of work.
Process Ownership & Standardization:
* Be responsible for the portfolio of global standards.
Establish and drive a governance and process for prioritization and lifecycle management, including creation, review and retirement.
* Develop, define, and own global customer service standards, ensuring they align with the overall strategy ...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:36
-
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 Deliver
Job Sub Function:
Deliver Excellence
Job Category:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
Johnson & Johnson is currently recruiting for a Director, CX&S Global Process Owner to be based in Raritan, NJ, Jacksonville, FL, Mirimar, FL, Markham, CA, Sao Paulo, BR, or Zug, CH.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United States - Requisition Number: R-010404
Switzerland- Requisition Number: R-010846
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Job Overview:
The person will be responsible for operational excellence and an outstanding customer experience by establishing and implementing the strategy for key business imperatives, driving connectivity across the business and enabling innovation, and strong operational performance.
The GPO will lead the global development, implementation, and continuous improvement of consistent processes and standards for customer service.
This role will ensure efficiency and high-quality customer interactions across all regions.
Key Responsibilities:
Strategic Project Management:
* Provide strategic oversight and program leadership for key global initiatives to innovate and improve operations, while maintaining quality services.
* Lead teams of regional partners and collaborate to define clear global scope, priorities, timelines, and requirements as well as alignment on regional/local customization needs for customer experience and service.
* Own global communications and business partner engagement.
* Lead global design requirements to support and enable the CX&S strategy.
* Identify and partner to address project dependencies to ensure success of the collective portfolio of work.
Process Ownership & Standardization:
* Be responsible for the portfolio of global standards.
Establish and drive a governance and process for prioritization and lifecycle management, including creation, review and retirement.
* Develop, define, and own global customer service standards, ensuring they align with the over...
....Read more...
Type: Permanent Location: Markham, CA-ON
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:35
-
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:
Pharmaceutical Sales
Job Sub Function:
Sales – Rare Diseases (Commission)
Job Category:
People Leader
All Job Posting Locations:
Mexico City, Mexico
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
Purpose and responsibilities:
- Supervises individual contributors (sales representatives) and/or Supervisors, and is accountable for driving sales in the Rare Diseases market and conducting effective performance management.
- Oversees functions pertaining to the sales strategy of Rare Diseases products and services, from maintaining awareness of the local and general market and adjusting sales tactics to maximizing revenue through leading and evaluating team members.
- Conducts regular business review meetings and develops innovative solutions to complex sales issues.
- Complies with established safety, privacy, and confidentiality guidelines.
- Develops value proposition for pipeline Rare Diseases products.
- Ensures understanding of brand strategies and aligned objectives.
- Generates insights and critical analysis of products to formulate marketing and selling strategies.
- Helps guide sales district in pursuit of strong competitive position and sales growth for Rare Diseases products through strategic and tactical planning (Win the Quarter, Win the Week) for identification of opportunities.
- Stays current on product knowledge, sales objectives, and industry developments to help determine key business drivers for the market development strategy and anticipate consumer needs for Rare Diseases products and/or services.
- Advises on how sales strategy may need to shift based on analysis of sales trends, new legislation, and relevant news in Rare Diseases, including competitive, business, and economic data, industry and trade journals/statistics, and ongoing intelligence from approved internal analytical sources and shares it with direct reports (sales reps - TM, KAL.).
- Responsible for managing operational aspects of their team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team g...
....Read more...
Type: Permanent Location: Mexico City, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:23
-
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:
MedTech Sales
Job Sub Function:
Inside Sales -- MedTech (No Commission)
Job Category:
Professional
All Job Posting Locations:
Columbus, Ohio, United States
Job Description:
We are searching for the best talent for Clinical Sales Specialist located in Columbus, OH.
About Orthopedics
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 Orthopedics? Ready to join a team that’s reimagining how we heal? Our Orthopedics 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
DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world.
DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide.
For more information, visit www.depuysynthes.com.
The overall responsibilities of the Clinical Sales Specialist position include advancing the Company’s sales of orthopedic surgical products by providing clinical and logistical expertise in hospitals and operating rooms - such as independent coverage of surgical cases, management of billing/purchase orders, logistics, and asset management.
Works under close supervision by management and in close partnership with Sales Consultants.
Key Responsibilities:
* Independently guide and assist surgeons in the operating room by providing clinical and technical support of orthopedic surgical cases.
* Advance DPS sales by serving as sole Company representative to provide direct customer support by attending surgeries and assuring that the proper equipment is available and functioning.
* Troubleshoot and apply independent judgment to respond to physician needs; address customer requests; effe...
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Type: Permanent Location: Columbus, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:22
-
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:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Innovative Medicine Research & Development Finance is recruiting for a Discovery, Product Development and Supply (DPDS) Senior Financial Analyst.
This candidate can work in our Spring House, PA or Titusville, NJ locations and will be required to travel to Spring House, PA, regularly.
This SFA will be responsible for providing financial leadership to the Therapeutics Discovery Function and will be an integral member of the Innovative Medicine DPDS Discovery Finance team by delivering on OPEX and CAPEX budget commitments, driving strategic business decisions, and providing recommendations on investment decisions.
Responsibilities:
Key activities for this position include, but are not limited to:
* Leading planning (JU & LRFP, NU, BP), Latest Thinking, and actual cycle budget updates for functional OPEX expenses (~$200MM across 2 VPs), headcount (~350 FTEs), and CAPEX expenses (~$45MM).
* Coordinating the budgeting process with business partners: budgeting, forecasting, and managing expenses and headcount.
* Supporting strategic investments by helping to develop business cases in partnership with functional business partners and by challenging business assumptions and guiding capital appropriation requests.
* Leading closeout efforts for capitalizable assets, managing and forecasting depreciation, and partnering with lab operations partners globally.
* Supporting ad hoc projects and applying financial analyses to provide recommendations for opportunities to drive new value within the organization.
* Identifying and implementing operational improvements / standardization of activities.
* Supporting FLDP and Co-Op on the team by providing coaching, mentoring, and crafting an environment of professional growth for the team.
Qualifications:
* Required
+ A minimum of a bachelor’s degree, preferably in Accounting or Finance.
+ A minimum of 3 years of finance or related business experience.
+ Proven financial and analytical skills, being result and performance driven.
+ Demonstrates business acumen and the ability to analyze complex financial problems, identify innovative solutions, and explain in...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:22
-
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:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
BE009 Turnhoutseweg 30
Job Description:
Johnson & Johnson is currently seeking a Quality Control – Micro analyst to join our CAR-T Hub located in Beerse.
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/.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Micro analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
The candidate will be part of the weekend team, working on Saturday and Sunday.
Working hours will be from 6am to 6pm.
Possibly preceded by training period in week regime.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP regulations.
* Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations.
* Perform peer review of laboratory data.
* Author and update SOPs, WIs and Protocols to support daily operations of the lab using the Document Management System.
* Support laboratory related investigation records and CAPAs.
* Assist in the execution of internal audits.
* Provide input to functional laboratory meetings.
* Provide input and take actions as a QC representative at cross-la...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:15
-
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 Deliver
Job Sub Function:
Deliver Excellence
Job Category:
Professional
All Job Posting Locations:
Jacksonville, Florida, United States of America, Miramar, Florida, United States of America, Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Director, CX&S Global Process Owner to be based in Raritan, NJ, Jacksonville, FL, Mirimar, FL, Markham, CA, Sao Paulo, BR, or Zug, CH.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Switzerland - Requisition Number: R-010846
Canada- Requisition Number: R-011032
Job Overview:
The person will be responsible for operational excellence and an outstanding customer experience by establishing and implementing the strategy for key business imperatives, driving connectivity across the business and enabling innovation, and strong operational performance.
The GPO will lead the global development, implementation, and continuous improvement of consistent processes and standards for customer service.
This role will ensure efficiency and high-quality customer interactions across all regions.
Key Responsibilities:
Strategic Project Management:
* Provide strategic oversight and program leadership for key global initiatives to innovate and improve operations, while maintaining quality services.
* Lead teams of regional partners and collaborate to define clear global scope, priorities, timelines, and requirements as well as alignment on regional/local customization needs for customer experience and service.
* Own global communications and business partner engagement.
* Lead global design requirements to support and enable the CX&S strategy.
* Identify and partner to address project dependencies to ensure success of the collective portfolio of work.
Process Ownership & Standardization:
* Be responsible for the portfolio of global standards.
Establish and drive a governance and process for prioritization and lifecycle management, including creation, review and retirement.
* Develop, define, and own global customer service standards, ensuring they align with the overall strategy and visi...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:14
-
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:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for Post Doctoral R&D Data Science and Digital Health, Real-World Evidence (RWE) Statistics
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 Real-world Evidence & Advanced Analytics team within Johnson and Johnson Innovative Medicines is looking for outstanding postdoctoral scientists whose responsibilities include:
* Analyze observational databases and historical trial data to generate real-world insight to support regulatory agency interactions
* Conduct literature reviews
* Create study protocols, statistical analysis plans, and statistical programming deliverables including analysis-ready data, tables and figures
Required qualifications:
* A Ph.D.
degree in Biostatistics, Statistics or epidemiology
* Expert coding skills using R
* Hands-on experience with data extraction, cleaning, and analysis, as well as statistical methods to mitigate confounding and selection biases
* Excellent interpersonal, communication and presentation skills
Preferred qualifications:
* Experience with real-world data sources (EHR, insurance claims, registry data)
* Familiarity with clinical trial data structure
* Subject matter knowledge in oncology, Immunology or Neuroscience
Johnson & Johnson is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
We actively seek q...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:14
-
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:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
San Diego, California, 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.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
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 the Associate Clinical Account Specialist position to be in San Diego, CA.
Purpose:
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of the Electrophysiology’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding business goals.
You will be responsible for:
Under (e.g.
limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and corporate Johnson & Johnson, procedures and guidelines, the ACAS will:
* Attend all portions of the ACAS fellowship training program without exception.
* Engage in dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during training.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
* Prioritize and appropriately respond to requests in a high-stress envi...
....Read more...
Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:11
-
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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Nonclinical Safety
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
Job Description:
We are searching for the best talent for a Principal Scientist, Toxicology, in the Specialized Applied Toxicology (SAT) group within Preclinical Safety and Translational Sciences (PSTS), to be located in Beerse, Belgium.
The successful candidate will be employed within our SAT group.
SAT is an international and diverse multidisciplinary team of scientists providing end-to-end portfolio specialized toxicology support including genetic toxicology, genomic safety, nonactive substance safety, occupational toxicology, and established product nonclinical safety.
As a member of our team, you will have a dual role.
Primarily, you will serve as a Nonclinical Safety Lead (NCSL) as an ad hoc member of established product (EP) compound development teams providing nonclinical expertise in emerging clinical safety issues, supporting periodic updates for marketed products, and representing PSTS on product labeling working groups.
Secondly, you will support the Nonactive Substance Safety (NASS) group as a toxicologist, the role includes providing end-to-end support to the J&J Innovative Medicine (IM) portfolio by delivering high-quality authored safety assessments of cross-modality (small and large molecule) Drug Substance (DS) and Drug Product (DP) impurities/degradants; residual solvents/elemental impurities; excipient toxicology assessments; product contact (manufacturing equipment and primary packaging) and drug delivery system Extractable/Leachable (E/L) toxicology assessments; and drug delivery system product biocompatibility assessments.
Key Responsibilities:
As an EP-NCSL:
* Serve as an ad-hoc member of compound development teams by providing relevant non-clinical expertise (pharmacology/pharmacokinetics/toxicology) to support Safety Man...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-25 08:10:10
