Job Description

QA Manager - Drug Product Clinical Manufacturing (m/f/d) - Quality Assurance / Pharmaceutical / cGMP / Synthetic Molecules / GMP Audits / SAP / Veeva / German / English

Project:

For our client, a large pharmaceutical company based in Basel, we are looking for a QA Manager (m/f/d) Drug Product Clinical Manufacturing (m/f/d).

Background:

The Synthetic Molecules IMP Quality Group is responsible for quality oversight of the Synthetic Molecules Drug Substance and Drug Product facilities, as well as the associated quality control. As an employee of the IMP Quality Organization Switzerland, you will ensure compliance with and continuous improvement of GMP compliance at the Drug Product IMP production facility in Basel.

The ideal candidate holds a Master's degree in Natural Sciences and has more than 10 years of professional experience in the pharmaceutical industry, including at least 5 years in quality assurance. They possess knowledge of cGMP and quality requirements for clinical development phases, as well as a proven track record of successful inspections. Strong computer skills and fluency in German and English complete the profile.

Tasks & Responsibilities:

Review of Drug Product Batch Records in collaboration with the relevant departments Conducting IMP Drug Product Release Review and approval of documents such as specifications, risk assessments, deviation reports, and change control records Review and approval of cleaning protocols and reports Supporting assigned departments with GMP-related issues Conducting self-inspections.

Must-haves:

Completed degree in a natural science, at least at Master's level. At least 10 years of professional experience in the pharmaceutical industry, including at least 5 years in quality assurance. Knowledge of cGMP and quality requirements for clinical development phases. Proven success in inspections by health authorities and internal GMP audits. Good computer skills (MS Office) - especially experience with SAP and other quality management systems (e.g., Veeva Vault). Fluent German and English, both written and spoken.

Nice to have:

Professional experience in the field of pharmaceutical development (Synthetic Molecules Drug Product).

Reference No.: 924664

Role: QA Manager - Drug Product Clinical Manufacturing (m/f/d)

Industry: Pharmaceuticals

Location: Basel

Workload: 100%

Start: ASAP

Duration: 12++ months

Application deadline: 12/01/2026

Job Type: 100%

Work Location: On the road