About Ardena Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to
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
CAI Overview Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver
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
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
Vacancy: Senior Quality Engineer For one of our clients in the pharmaceutical sector, we are looking for an experienced Senior Quality Engineer. In this role, you will be responsible for ensuring and improving quality, compliance, and
Senior Quality Engineer | Engineering, Validation & Maintenance (EVM) Job Description A leading global pharmaceutical and biotechnology organisation is seeking a Senior Quality Engineer to join its Engineering, Validation & Maintenance (EVM) department at a major
Job Role: Senior Quality Engineer About the Role: We are seeking an enthusiastic and dedicated professional to join the Engineering-Validation-Maintenance (EVM) team at a leading pharmaceutical company in Leiden. This role focuses on ensuring GMP compliance,
For our Engineering department (industrial automation) we are currently looking for a CSV Specialist. As a CSV Specialist you optimize and maintain the Computerized systems management and validation procedures and ensure optimal execution and continuous improvement
JOB SUMMARY The CQV Engineer is responsible for supporting and executing Commissioning, Qualification, and Validation (CQV) activities across a wide range of systems—including HVAC, utilities, and process equipment—in regulated industries such as pharmaceuticals, biotechnology, or life
Byondis is an independent Dutch biopharmaceutical company, based in Nijmegen, that focuses on developing innovative medicines against cancer and autoimmune diseases. Our values integrity, authenticity, entrepreneurship, quality and trust are very highly regarded. We are driven
Overview The Role We have an exciting opportunity for a Bulk Bio SME to join our team.The role is to work as a Subject Matter Expert providing technical leadership on Bulk Bio. As a member of