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QA Specialist
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-09-01
Listing for:
CTC Resourcing Solutions
Full Time
position Listed on 2026-09-01
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Production QC/QA, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers -
Pharmaceutical
Regulatory Compliance Specialist
Job Description & How to Apply Below
Our client, a global pharmaceutical company, is looking for a QA Specialist to support Quality Assurance activities related to Investigational Medicinal Products (IMPs).
The role focuses on GMP documentation review, quality system activities, batch documentation, and coordination with Contract Manufacturing Organizations (CMOs). The successful candidate will contribute to ensuring that QA operations remain compliant, timely, and inspection-ready.
Key Responsibilities- Review GMP documentation and executed batch records for completeness and compliance.
- Support QA release activities for Investigational Medicinal Products (IMPs).
- Identify, document, and escalat discrepancies and quality issues.
- Prepare and maintain batch documentation packages.
- Manage QA documentation within electronic document management systems (eDMS), including Veeva Vault.
- Maintain accurate QA-related records and batch information in ERP systems such as SAP.
- Track deviations, change controls, complaints, temperature excursions, and other quality events.
- Perform initial reviews of investigations received from CMOs.
- Coordinate with internal stakeholders and external manufacturing partners to ensure timely resolution of quality topics.
- Support the maintenance and review of Quality Agreements with CMOs.
- Collect and consolidate CMO quality metrics and contribute to KPI and trend reporting.
- Ensure QA documentation remains accurate, complete, and inspection-ready.
Skills & Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field
. - 1–3 years of experience in QA, QC, pharmaceutical manufacturing, or a similar GMP environment.
- Good practical knowledge of GMP/GDP principles
. - Experience reviewing GMP documentation such as batch records, deviations, and change controls
. - Strong organizational and time-management skills, with the ability to manage multiple priorities.
- High attention to detail and a structured, process-oriented approach.
- Ability to identify quality issues, propose solutions, and escalat appropriately.
- Strong written and verbal English communication skills
. - German and/or French would be an advantage.
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