Global TRD QA Project Manager – Medical Devices (Basel)

EDP Personalberatung GmbH; Basel; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Benefits dieser Stelle

Flexible working hours

Extensive training opportunities

Multicultural team

Zusammenfassung

EDP Personalberatung GmbH is assisting a Basel-based pharmaceutical company in recruiting a Project Manager in Medical Device/QA. The role is a temporary 100% position in Basel, with a contract from 01.01.2027 to 31.12.2027 and an option for extension.

You will lead global TRD QA activities, ensure quality oversight on development projects, and drive QA strategy in line with cGMP guidelines. The ideal candidate holds a Bachelor (or higher) with 10+ years in pharma quality or operations, fluent

Qualifikationen

• Bachelor/Master degree with pharma quality or operations experience.
• Experience with regulatory inspections (FDA/EMA) and health authority interactions.
• Knowledge of cGMP and quality standards in drug product/medical devices.
• Proven track record in QA/Quality Assurance and cross-functional teams.

Aufgaben

• Lead and represent TRD QA in global project teams and QA board meetings.
• Ensure quality oversight on development projects per cGMP and TRD QA guidelines.
• Contribute to project strategy, risk assessments and contingency planning.
• Coordinate interactions between TRD QA and other departments.
• Prepare and guide TRD project teams for Mock-PAI and PAI processes.
• Lead cross-functional initiatives.

Kenntnisse

English fluency

German or French

Quality systems knowledge

FDA/EMA inspections

Combination products

Cross-functional collaboration

Ausbildung

Bachelor Degree

Masters Degree

Jobbeschreibung

EDP Personalberatung GmbH is assisting a Basel-based pharmaceutical company in recruiting a Project Manager in Medical Device/QA. The role is a temporary 100% position in Basel, with a contract from 01.01.2027 to 31.12.2027 and an option for extension.

You will lead global TRD QA activities, ensure quality oversight on development projects, and drive QA strategy in line with cGMP guidelines. The ideal candidate holds a Bachelor (or higher) with 10+ years in pharma quality or operations, fluent