Job Description

QA Manager (m/f/d)
Location: Allschwil, Switzerland
Workload: Full-time (100%)
Start Date: ASAP
Duration: 12 months (with possible extension)
Overview:
CK QLS are partnered with a leading global pharmaceutical organization seeking a QA Manager, to support product development and manufacturing activities within a GMP/GDP-regulated environment. This position plays a key role in ensuring quality assurance across the product lifecycle, and contributes directly to continuous improvement initiatives in the pharmaceutical quality system.
Key Responsibilities:

• Provide QA oversight and support throughout the product development lifecycle.
• Manage release of active pharmaceutical ingredients and investigational/commercial medicinal products.
• Evaluate and process deviations, CAPAs, OOS investigations, and change controls.
• Represent QA in cross-functional development teams and project meetings.
• Participate in audits and ensure documentation compliance.
• Drive enhancements to the pharmaceutical quality system and support process improvement.

Candidate Profile:

• Master's degree (or higher) in Pharmacy, Chemistry, or a related scientific field (PhD/PharmD preferred).
• Several years of relevant experience in QA and pharmaceutical development or manufacturing.
• Strong working knowledge of GMP/GDP and regulatory frameworks (EU and global).
• Excellent communication skills in English; proficiency in German or French is a plus.
• Structured, proactive and team-oriented working style.

The Offer:

• Collaborative, international team environment.
• Up to 3 days/week home office option.
• Competitive compensation package.
• Opportunity to contribute to global development projects in a mission-driven organization.
• Career growth potential in a recognized leader in the life sciences industry.

Apply:
All applicants must have the right to work in Switzerland. Please quote 145 553 in all communication.