Senior Associate QA (GMP)
Hays
Senior Associate QA (GMP)
Samenvatting
Wat krijg je?
Wat ga je doen?
- Review and approve batch records
- Support investigations and deviations
- Conduct GMP compliance checks
- Manage quality-related production queries
- Contribute to SOP development
Wat verwachten wij?
- Degree in Pharmaceutical, Life Sciences or Biotechnology
- Three years experience in QA or manufacturing
- Experience with batch records, deviations and investigations
- Strong knowledge of GMP, GDP or GCP
Volledige vacaturetekst
Join a leading global biopharmaceutical organisation dedicated to improving patients' lives. As a QA Specialist, you provide essential support within a dynamic production environment, ensuring GMP compliance through batch record reviews and investigations. You benefit from a generous travel allowance and the chance to work within an innovative, highly regulated field. Ready to elevate your career in quality? Discover how you can make a real impact and apply today.
Your new company
Join a leading global biopharmaceutical organisation dedicated to improving patients' lives through the development, manufacturing, and distribution of innovative healthcare products. The company operates in a highly regulated GMP environment and is committed to quality, compliance, and continuous improvement. This position is based within a dynamic production quality team, working closely with Production, Engineering, Warehouse, and Quality stakeholders.
Your new role
As a QA Specialist, you will provide quality assurance support within the production environment, ensuring compliance with GMP standards throughout packaging, labelling, and manufacturing activities. You will review and approve batch records, support investigations and deviations, conduct GMP compliance checks, and serve as the first point of contact for quality-related production queries. In addition, you will contribute to SOP development, training activities, quality improvement projects, and performance reporting.Please note this role operates in a 5-shift pattern. Full commitment to the following schedule:
- Early Shift: 06:30-15:00
- Late Shift: 14:30-23:00
- Night Shift: 22:30-07:00
- BSc or MSc degree in Pharmaceutical Sciences, Life Sciences, Biotechnology, or a related field.
- Minimum 3 years of experience in Quality Assurance or pharmaceutical manufacturing.
- Experience with batch record review, deviations, investigations, and GMP-regulated processes.
- Strong understanding of GMP, GDP and/or GCP regulations.
- Experience supporting manufacturing or quality operations within the pharmaceutical or medical device industry.
- Excellent communication and stakeholder management skills.
- Ability to work independently, multitask, and perform effectively in a fast-paced production environment.
- Fluent in English, both written and spoken.
- Willingness and ability to work a rotating 3-shift schedule.
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. An extension to stay within the department is anticipated. In this position, you will get a competitive salary starting at €4400 bruit per month and your travel expenses are covered.
What you need to do now
If you're interested in this role, click 'Apply Now' to forward an up-to-date copy of your CV, or contact us for more information.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.#1050447
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