Key Responsibilities:
- Provide QA guidance and support in the production area.
- Perform batch record review of batches assembled, packaged and labeled before production activities take place.
- Triage and manage production floor issues (e.g., jams, material incidents, deviations).
- Perform finished product checks during (commercial) production runs.
- Assist in various investigations, as needed.
- Responsible for preparation of weekly/monthly metrics.
- Perform GMP compliance checks in production.
- Establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person.
- MBO, Bachelor's or Master's degree in Life Sciences, Pharma, or equivalent experience.
- 3+ years in a regulated industry (pharmaceutical, medical device or food).
- Quality Assurance experience is a Must.
- Strong understanding of GMP/GDP and compliance requirements is an advantage.
- Flexible to work 100% on-site in a 3-shift structure in Breda. Holding a driver's license and owning a car therefore is highly preferred.
- Stress-resilient and able to multitask under pressure.
- Assertive with strong communication and stakeholder management skills.
- Fluency in English, both written and verbal.
- A challenging, international work environment with excellent career development programs.
- A competitive salary package.
- 40-hour workweek.
- Reimbursement of travel expenses is dependable on travel distance.
- The contract will be through Undutchables.
Salarisomschrijving
€4700.00 - €4700.00 monthly
