Product Quality Lead Pharma GMP Lifecycle Management
Product Quality Lead Pharma GMP Lifecycle Management
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Salary Not Disclosed
1 Vacancy
Job Description
6Month Temporary Contract Basel
Our client is a leading biopharmaceutical company dedicated to providing innovative treatments for rare diseases. To strengthen their Global Quality team they are seeking an experienced Product Quality Lead (m/f/d) for a 6month contract. This role will be split between leading a quality improvement project and managing product quality oversight for commercialized pharmaceuticals.
Your Role & Responsibilities
Quality Improvement Project 50
- Lead a crossfunctional quality improvement initiative focused on streamlining change control handling in regulatory dossiers and release processes.
- Ensure compliance with GMP regulations and pharmaceutical quality standards.
- Provide project management support including planning scheduling and coordination of activities.
- Collaborate with stakeholders to drive process efficiency and ensure successful implementation.
Product Quality Lead Responsibilities 50
- Act as key Quality Assurance contact for 13 medicinal products ensuring compliance throughout their lifecycle.
- Provide assessment guidance and regulatory oversight on all product quality aspects.
- Support crossfunctional teams involved in product lifecycle management.
- Ensure audit and inspection readiness in collaboration with internal teams.
Your Profile
- Educational Background: University degree (minimum 4 years) in Pharmacology Biochemistry Chemistry Chemical Engineering or equivalent.
- Industry Expertise: At least 5 years of Quality Assurance experience in commercial pharmaceuticals under GMP.
- Regulatory & Compliance Knowledge: Strong understanding of EU/FDA GMP requirements regulatory dossiers and release processes.
- Project Management: Proven track record in pharmaceutical project management ideally with complex supply chains & CMO/CLO management.
- Communication & Leadership: Excellent stakeholder management skills with the ability to work collaboratively in a global team environment.
- Language Skills: Fluent in English (spoken & written).
Whats in for You
6month interim contract in a global biopharmaceutical company.
Exciting opportunity to lead a highimpact quality improvement project.
Work in Basel Switzerland with a flexible hybrid model (minimum one day onsite required).
Are you ready to take on this highimpact Quality Assurance role Join a leading pharmaceutical company and drive excellence in GMP compliance.
Employment Type
Full Time
