**#QA #TRD #GMP #R&D #SOP #German&English**

Our customer, a
**pharmaceutical company**
based in
**Basel**
, needs reinforcement. For a
**temporary employment**
(asap – for 6 months, with option for extension) we are looking for a
**QA Manager**
.

**QA Manager (m/f/d), 100% (temporary)**

Beschäftigungsort: Basel

Beschäftigungsgrad: Temporärstelle

Einsatztermin: ab sofort

**Benefits**

- An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
- Flexible working hours and extensive training opportunities
- A motivated multicultural team and environment

**Your main responsibilities**

- Batch release of clinical supplies (packaged and labeled finished goods, materials, and components), including review and approval of GMP documentation and issuance of batch certificates.
- Deviation, and incident management: evaluation, QA oversight, support to investigations, and approval of records.
- Change control management for GCS processes and documentation.
- Write, review, and approve GMP-relevant documents (SOPs, CoAs, risk assessments, checklists, packaging & labeling documentation).
- Support audits and inspections for TRD GCS topics.
- Provide QA support for GCS operations and ensure alignment with TRD QA standards.

**Your Profile**

- Master’s degree in life sciences or equivalent education.
- 3–5 years of Pharma QA experience, ideally in development, manufacturing, packaging, or clinical supply.
- Strong knowledge of cGMP and QA processes (batch release, deviations, changes).
- Hands-on experience with SAP (materials management, batch records, release workflows).
- Experience with 1QEM is a strong asset.
- Excellent communication and decision‑making skills.
- Fluent German and English (oral & written).

**Nice to have:**

- Experience in packaging and labeling operations or in global clinical supply chains.
- Experience collaborating with CMOs or external partners.

Fragen?

Für Fragen steht dir Renato Imboden gerne telefonisch unter +41 61 269 90 65 zur Verfügung.