Quality Assurance Manager, Pharma, Schaffhausen, Contract

We have a 11 Month Contract opportunity available in the canton of Schaffhausen, Switzerland with a global Pharmaceutical company for a Pharmaceutical professional to work actively on their Product Quality Review (PQR) reporting. The role requires fluent German speaking and at least 3 years of direct experience in Quality Assurance for Pharmaceutical/Biotech environment, prior experience in PQR is preferred but not essential. There is a competitive Hourly rate for the role, please see further information below:

RESPONSIBILITIES

-Author Annual Product Review (APR) and Product Quality Review (PQR) reports independently for products with complex supply chains.
- Quality Data collection in various Quality Systems and Databases.
- Perform comprehensive assessment of product quality by analysing/evaluating end-to-end APR/PQR data to ensure state of control for manufacturing processes, specifications and control systems.
- Collaborate and communicate with all site APR/PQR business process managers, global/network functions and Quality Product Leaders to ensure timely and accurate APR/PQRs are provided and analyses lead to appropriate conclusions.

REQUIREMENTS -BA, BSc or higher degree (preferably in Life Science or Engineering) and at least 3 years of experience in the pharmaceutical or biopharmaceutical industry.
- Work experience in Quality, Pharmaceutical Manufacturing or Process Development as well as local site and emerging markets experience are required.
- Knowledge of product manufacturing processes and quality processes and systems as well as knowledge of the regulatory environment.
- Hands-on experience with Annual Product Review/Product Quality Review documents is preferred.
- Fluent verbal and written communication skills in English and in German required.
- Excellent technical writing/editing skills including proficiency in MS Word, Excel, and PowerPoint. Experienced in generating and presenting complex data graphs and reports.
- Ability to manage and influence stakeholders to deliver supporting information on time is crucial to be successful in this role.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.

Best regards,

Michael Kellitt

MBA Michael Bailey Associates AG

Job Code: 108604 (internal)/ (external)

Key words: Quality Assurance, GMP, GxP, Compliance, Freelance, Qualität, Qualitätskontrolle, Pharmaceutical, Life Science, Biotech, Generic, cGMP, Quality Enginee, Ingenieur

Michael Bailey International is acting as an Employment Business in relation to this vacancy.