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The following information aims to provide potential candidates with a better understanding of the requirements for this role.
If you have 4+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE ROLE: Maintenance of External Supply Quality licenses as it relates to global GMP/GDP activities (MIA, ASR, WDA).
Ensuring the review, and where appropriate, preparation and regular update of Quality Agreements with outsourced partners.
Owner and approver of GMP/GDP QMS documents.
Support the annual Quality Management Review meeting and co-ordination of any actions from this meeting for implementation.
Preparation and periodic review of Bona Fides.
QA approval of deviations/non-conformances ensuring deviations are fully investigated and that remedial measures are implemented to address the root cause of failures and relevant actions are taken to prevent their re-occurrence.
QA approval of change control proposals (third party contractors and internal) and action plans.
ARE YOUR SKILLS A MATCH: Doctorate degree OR Master's degree & 2 years of directly related experience OR Bachelor's degree & 4 years of directly related experience OR Associate's degree & 10 years of directly related experience.
4+ years of quality and manufacturing experience in biotech or pharmaceutical industry.
Apply today directly through this advert or contact Kathy Gillen on for further information.
All applicants must hold a valid work permit and visa for at a least 12 months. xcfaprz
LSC cannot provide work permit sponsorship.
Skills: Quality Quality Assurance Management Pharmaceutical QA Manager
Sprachkenntnisse
- English
Hinweis für Nutzer
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