Join to apply for the Quality Assurance Manager - RP Deputy role at Michael Page
Join to apply for the Quality Assurance Manager - RP Deputy role at Michael Page
About Our Client
International pharmaceutical group with a growing biopharma portfolio is seeking a QA Manager / Responsible Person Deputy to join its Swiss office in Geneva. Opportunity to contribute strategically to quality oversight, regulatory compliance, and business-critical projects across a dynamic and expanding portfolio.
* Pharmaceuticals QA
* International operations
About Our Client
International pharmaceutical group with a growing biopharma portfolio is seeking a QA Manager / Responsible Person Deputy to join its Swiss office in Geneva. Opportunity to contribute strategically to quality oversight, regulatory compliance, and business-critical projects across a dynamic and expanding portfolio.
Job Description
Key Responsibilities for the Quality Assurance Manager / RP DeputyQuality Systems & Processes
* Lead and maintain assigned quality processes, including complaints, deviations, and change controls
* Drive continuous improvement of the QMS and overall quality culture within the organisation
Third-Party Oversight
* Manage quality oversight for assigned contract manufacturers and partners
* Ensure compliance through QTAs, audits, deviations, change management, and performance monitoring
Project Quality Leadership
* Act as Quality Lead on assigned cross-functional projects
* Define, implement, and monitor quality requirements in accordance with internal SOPs and external regulations
* Drive quality assurance from project initiation through to delivery
QMS & Audit Contribution
* Support the development and implementation of SOPs, KPIs, and training
* Plan and execute internal and external audits
RP Deputy Responsibilities
* Provide support to the RP as required, including compliance with Swissmedic expectations
* Step in as RP delegate when necessary
The Successful Applicant
Your ProfileEducation
* Pharmacist degree or MSc in Biological/Pharmaceutical Sciences (or equivalent)
Experience
* Minimum 10 years of QA experience within pharmaceuticals or biologics
* Proven background in managing QA for outsourced manufacturing-experience in biologics or vaccines is a distinct advantage
* Familiarity with QA systems and digital tools
Knowledge & Skills
* Strong knowledge of EU GDP, GMP (EU & US), and Swissmedic regulations
* Understanding of the RP function under Swiss law
* Strong analytical mindset and ability to work autonomously
* Excellent communication and cross-functional collaboration skills
* Fluent in English.
What's on Offer
What We Offer
* A high-impact role in a fast-growing biologics and vaccines business
* The opportunity to influence QA strategy and operations across international markets
* A dynamic and collaborative work environment in the Geneva life sciences hub
* Competitive compensation and relocation support if required
Contact: Charly Ble
Quote job ref: JN-072025-6778959
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Science and Health Care Provider
* Industries
Staffing and Recruiting
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