Quality Assurance Production Specialist
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Quality Assurance Production Specialist in Haarlem, Noord-Holland, farmaceutische productie, start 26 augustus 2026.
- Locatie
- Haarlem
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
Eisen
- Skills in training, knowledge transfer, and teamwork
- Knowledge of aseptic pharmaceutical processes and production control systems
- Ability to thrive in a dynamic, regulated setting with attention to detail and quality
- Master's degree or equivalent in Pharmacy, Chemical Engineering, or a related field
- Proficiency in English, both spoken and written
- Experience working within pharmaceutical manufacturing environments
- Strong communication, analytical, planning, and reporting skills
Omschrijving
A leading organization in the pharmaceutical manufacturing sector is looking for a Quality Assurance Production Specialist in Haarlem, Noord-Holland. The role involves overseeing and supporting pharmaceutical production processes to ensure compliance with quality standards, evaluating production activities, supporting quality improvement projects, and maintaining strict adherence to GMP regulations. Responsibilities include ensuring quality assurance within pharmaceutical production (bulk manufacturing and packaging), supporting production teams in managing deviations and quality issues (including deciding whether to halt production), proposing and implementing improvements to manufacturing processes and technology, providing technical and content support regarding quality matters (monitoring, investigating, documenting deviations and complaints), conducting root cause analyses and developing CAPAs, leading process improvement initiatives from audits or deviations, advising on occupational health and safety, product safety and environmental policies, participating in audits and investigations, maintaining documentation (SOP reviews, validation protocols, batch records), contributing to project work, change controls and staff training, and engaging in business unit meetings with internal and external stakeholders. Requirements: Master's degree or equivalent in Pharmacy, Chemical Engineering or a related field; knowledge of aseptic pharmaceutical processes and production control systems; experience in pharmaceutical manufacturing environments; strong communication, analytical, planning and reporting skills; proficiency in English (spoken and written); ability to thrive in a dynamic, regulated setting; skills in training, knowledge transfer and teamwork. Start date 8/26/2026, job ref 58817.
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