QA Manager - Drug Product klinische Herstellung

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: 16/02/2026

Should this position have sparked your interest, please send us your complete application. If this position isn't quite the right fit and you'd prefer to be notified directly about other opportunities, you can also submit your application via this advertisement or to jobs[at]itcag[dot]com.

For further information about our company, our open positions, or our attractive payroll-only program, please contact us at +41 41 760 77 01.

About us:

ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in placing highly qualified candidates for temporary staffing in the IT, Life Science, and Engineering sectors. We offer both temporary staffing and payroll services. These services are free for our candidates, and we do not charge any additional fees for payroll.

ITech Consult AG

+41417607701