At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
JOB DESCRIPTION: Abbott is een wereldspeler op het gebied van gezondheid en streeft ernaar mensen niet alleen een langer, maar ook een beter leven te geven. Bij Abbott werken wereldwijd 100.000+ medewerkers in 150 landen aan
QA Team Leader II Geleen, Netherlands – Primarily Site-Based Join a team that helps deliver life-changing therapies to patients around the world. As a QA Team Leader II, youll lead a team of Quality Assurance professionals, ensuring the
BandLevel 3 Job Description SummaryThe Quality Assurance Operations Specialist provides QA support for all shopfloor GMP related activities. The main focus is linked to the on-time batch release process and all related operational activities to ensure that the
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Description A newly created highly visible leadership role, focused on strengthening and centralizing analytical method transfer capabilities for Large Molecules across the EU/APAC network. For our Animal Health location Boxmeer, we are currently recruiting an
Job Description Act at the interface of R&D and QC and use your commercial pharma experience to support robust method transfers, minimize supply risk, and support on-time product releases. For our Animal Health location Boxmeer, we
Salary Range:€58,900.00 - €109,300.00 Job Description Summary#LI-Onsite Location: Baarle-Nassau, The Netherlands This role is based in Baarle-Nassau, The Netherlands. Novartis is unable to offer relocation support for this role: please only apply if this location is
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and
Customer Experience Quality Lead Department: Customer Experience Employment Type: Full Time Location: Duiven, Netherlands Reporting To: Leo Trigo Description About the role: As QA Lead, you will own the quality of every customer interaction across the Arcavindi
Drive meaningful change Are you ready to combine your role as Qualified Person with leading and developing a team of experienced QPs in an international environment? We are looking for an experienced and people-oriented Manager, who
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and
Production Team Lead – Cell & Gene Therapy Manufacturing (EU Applicants Only) Location: Geleen Contract: Permanent Start Date: ASAP Working Pattern: 24/7 rotating shift schedule (day, evening, night) On-site role (no hybrid option due to GMP
Senior QA Officer – Batch Record Review & Deviation Management Position Summary We are seeking an experienced Senior QA Officer to join a leading pharmaceutical manufacturing organization. The successful candidate will be responsible for batch record review, deviation management, and