Qualification & Validation Lead – CSV, Basel (Remote)

For one of our clients, a leading global pharmaceutical company, we are currently looking for a Qualification and Validation Manager. General Information: Workplace: Basel Remote/Home Office: possible, max 20% Working hours: Standard Department: MSAT (MMNGF) Team: 10 people About the job: The Qualification Manager is responsible for the CSV and qualification...

A leading global pharmaceutical company is seeking a Qualification and Validation Manager in Basel. The role requires a Master’s degree and over 2 years of experience in a cGMP environment. Responsibilities include managing qualification projects and collaborating with engineering teams. Candidates must have excellent communication skills in German and...

ABOUT ARCONDIS Wir schaffen Mehrwert durch funktionsübergreifende, ausgefeilte Projektabwicklung und intelligente Implementierung. Unsere Kunden lieben die Zusammenarbeit mit uns aufgrund unserer einzigartigen Fähigkeiten, unseres pragmatischen Ansatzes und unseres unbedingten Erfolgswillens. We make healthcare better. MISSION Tasks and...

A healthcare company is seeking an experienced Enterprise Quality R&D Clinical Computer System Validation Manager in Basel to manage Computer System Validation (CSV) within a compliance framework. Responsibilities include ensuring quality standards, leading validation activities, and managing teams for GxP systems. Ideal candidates will have extensive...

A global leader in life sciences is seeking a Global MSAT Drug Product Qualification and Validation Lead to oversee manufacturing process control strategies. The ideal candidate will have a Ph.D. in pharmaceutical sciences, substantial experience in process validation for sterile manufacturing, and strong leadership skills. This role offers opportunities to...

A recruitment agency for life sciences is looking for a Process Validation Engineer to lead validation activities and develop protocols for new drug tech transfer. The role requires expertise in GMP standards and strong data analysis skills. Candidates should hold a relevant degree and have experience in the pharmaceutical or biotech sectors. This position...

Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager Join to apply for the Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager role at Johnson & Johnson. Location: Horsham, PA; Raritan, NJ; Beerse, Belgium or Allschwil, Switzerland. About the Role Enterprise Quality (EQ) manages the Quality and Compliance strategy for...

A leading global pharmaceutical company in Basel is seeking a Qualification and Validation Manager. The ideal candidate will possess a Master's degree in chemical engineering or biotechnology and have over two years of experience in a GMP environment. Responsibilities include managing qualification projects and ensuring compliance during authority...

**JOB DESCRIPTION** For 25 years, the **ATP-CGPharm Group** has been supporting clients in the Life Science Industry with a broad range of services in GxP engineering, commissioning, qualification & validation, quality assurance, quality control and environmental monitoring. The group operates internationally with offices in France and Switzerland. If you...

CSV Specialist (Maintenance) – Planet Pharma Job Description CSV Maintenance Specialist – SwitzerlandAre you a passionate Quality and Compliance professional ready to make a real impact in the pharmaceutical industry? Join a pioneering, fast‑growing CDMO dedicated to developing and manufacturing life‑saving injectable medicines. As a CSV...