QA Release Manager

Highly Competitive
  1. Contract
  2. Good Distribution Practice (GDP)
  3. Switzerland
Basel-Country, Switzerland
Posting date: 26 Nov 2024
63333

Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry!
Have a look below and apply or send me your CV directly.

Proclinical is seeking a Quality Assurance Release Manager for a temporary contract position of 12 months based in Aesch, Switzerland.

Join the team and be part of an innovative company that values inclusion, growth, and impact. The dynamic work environment offers brilliant opportunities for advancement. They are seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • The QA Release manager is expected to actively engage in batch record review and batch release decision-making process currently serving three different categories of products (Pharmaceuticals (APIs), Diagnostics (IVD/MD) and Cosmetics).
  • Assures products sold shall comply with all relevant quality requirements and are safe for their intended use.
  • In collaboration with the peer group of other QA Managers, the QA Release manager supports continuous development of the various norms and legislation requirements and translates those in line with the company's needs.
  • Despite applying identical internal processes, the person needs to consider the requirements of the specific regulatory environment and must be able to adapt the decision-making process accordingly.
  • Performs and reports internal and external audits according to the annual auditing plan. Assures adequate follow up and closure.

Key Skills and Requirements:

  • Academic degree (BSc and/or MSc) in life science (chemistry, biochemistry, pharmacy, biotechnology).
  • High degree of knowledge in GMP and cGMP for Pharma and Medical Device Industry, ISO, Cosmetics GMP.
  • Proven working experience in areas of quality assurance, quality control or production in the pharmaceutical, diagnostic and/or cosmetic industry.
  • Practical experience in a cGMP/ISO production environment with multidisciplinary interaction with all relevant company functions on a daily base.
  • Fluent in German is a necessity as well as English both written & spoken.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com



Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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