QA Manager (m/w/d)

QA Manager (m/f/d), Manufacturing Unit Monoclonal Antibodies (MAB) - Quality Assurance/ GMP Compliance/ GMP/ German/ English

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

Background:
The Basel Drug Substance division at the Group headquarters in Basel is divided into various production units for monoclonal antibodies (MAB), single-use technology (SUT), antibody drug conjugates (ADC), and synthetic molecules (SM). Within this dynamic environment, the Quality Assurance (QA) team ensures compliance with the highest quality standards and drives continuous process improvement. Organizationally, the QA managers belong to one of the three QA Operations Chapters (MAB ADC & SUT or QA SM & Direct Materials).

As Quality Assurance (QA) Managers for Direct Materials, QA Managers make a critical contribution to quality oversight through the qualification and release of raw materials. In this role, they are responsible for ensuring compliance with and continuous optimization of the quality system, always taking into account current legal and internal Roche requirements. Through changing assignments, they expand their network and actively contribute to the harmonization of processes.

The perfect candidate: has a university degree in a scientific or engineering field (e.g. biology, chemistry, pharmacy, biotechnology) and at least 1-3 years of professional experience in the field of quality assurance or GMP compliance, or at least 3 years in a GMP regulated work environment.

Tasks & Responsibilities:
• Central contact person for purchasing, QC and production facilities for all quality issues, raw material release and qualification.
• Ensuring quality oversight and GMP compliance for the raw materials and projects managed.
• Reviewing, assessing and approving specifications, both on paper and in SAP/SLIMs
• Responsible for the release of direct materials
• Processing, assessing and approving deviations, corrective actions (CAPAs) and technical change requests.
• Self-inspections and supporting internal audits and official inspections.
• Actively contributing ideas for the continuous improvement of processes and supporting their implementation.

Must Haves:
• Completed university degree in a scientific or engineering field (e.g. biology, chemistry, pharmacy, biotechnology)
• At least 1 year of professional experience in the field of quality assurance or GMP compliance, or 3 years in a GMP regulated work environment
• Strong team player with excellent communication skills
• High quality awareness and an independent, result-oriented and assertive way of working
• Fluent communication in German and English (spoken and written)
• Proficient in the use of common IT systems in the pharmaceutical industry

Reference No .: 924517
Role: QA Manager (m/f/d), Manufacturing Unit Monoclonal Antibodies (MAB)
Industry : Pharma
Location : Basel
Workload: 80 - 100%
Start: 01.01.2026
Duration: 8+ months (latest possible start date: 01.02.2026)
Application deadline : 29/10/2025

If this position has piqued your interest, please send us your complete application. If this position doesn't match your profile and you'd like to apply directly for another position, you can also send us your application via this advertisement or to jobs[at]itcag[dot]com.
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About us:
ITech Consult is an ISO 9001:2015-certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in the placement of highly qualified candidates for temporary staffing in the IT, life sciences, and engineering sectors. We offer temporary staffing and payroll services. This is free of charge for our candidates, and we also do not charge any additional fees for payroll.