Quality Assurance Consultant (m/f/d)
Responsibilities
- Reviewing the Batch Record of the CMO with the intent to ensure that the Packaging and Labelling activities have been performed as per the defined steps in the batch record in accordance with current GMP Guidelines and the approved dossier
- Supporting the distribution to commercial partners, e.g. with establishment of Quality Agreements, assessing temperature excursions, improving documentation standards
- Assessing the training assignment identifying gaps and redundancy, support in defining the required training assignment and implementing them in the training system
- Harmonizing local governing documents and support in developing shared regional procedures
Profile
- Educated in Pharmaceutical Technology, Chemistry, Biology or comparable scientific background.
- Solid experience in Good Manufacturing or Good Distribution Practice regulated activities in Manufacturing or QA
Benefits
- Interesting working environment and exciting tasks
- Support during the entire recruiting process
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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