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Quality assurance manager - rp deputy

Genf
Michael Page
EUR 120’000 pro Jahr
Inserat online seit: Veröffentlicht vor 20 Std.
Beschreibung

* 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 Deputy



Quality 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 Profile



Education

* 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
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