Senior Production Expert, Haarlem, Noord-Holland

Location: Haarlem, Noord-Holland  |  Sector: Pharmaceuticals  |  Start Date: 8/25/2026  |  Job ref: 58798

Company:
A leading organization in the pharmaceutical industry dedicated to ensuring the highest standards of quality and safety in drug manufacturing. The company is committed to continuous improvement, compliance, and innovation within its production facilities.

Job Description:
We are seeking a dedicated Pharmaceutical Production Quality Specialist to join our client's team. The successful candidate will play a key role in maintaining and enhancing quality assurance processes within pharmaceutical production, ensuring compliance with GMP standards and company protocols.

Responsibilities:
-Oversee and support all quality assurance activities within the production environment, including bulk manufacturing and packaging operations.
- Assist with handling deviations, quality issues, and supporting production to resolve them effectively.
- Evaluate whether production processes should be paused in response to deviations and ensure timely decisions are made.
- Contribute to the development and implementation of improvements in production methods and technology.
- Provide technical support on quality topics, monitor production processes, report deviations, and investigate root causes.
- Document and manage CAPAs, investigate complaints, and ensure proper closure of quality incidents.
- Develop and implement continuous improvement initiatives based on audit observations, deviations, and industry best practices.
- Ensure compliance with GMP standards by reviewing SOPs, validation protocols, batch records, and related documentation.
- Support ongoing training, knowledge transfer, and participation in quality and compliance projects.
- Engage with internal teams such as production management, QA, operators, and external partners as needed.

Requirements:
- Master’s degree or equivalent in Pharmacy, Chemical Engineering, or a related field.
- Strong knowledge of aseptic pharmaceutical processes, GMP, and production control systems.
- Previous experience in a pharmaceutical production environment is essential.
- Excellent communication, analytical, planning, and organizational skills.
- Proficiency in English, both spoken and written.
- Ability to work effectively in a fast-paced, dynamic environment with a results-oriented approach.
- Strong team player with a collaborative mindset and a focus on quality.

Other Information:
If you are interested and want to apply, please submit your application via the apply button below and contact me. 

58798

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