Job Summary
Management of the Production Quality Management system in line with QS procedures. Management of the QA Production section to provide proper control and support to manufacturing and supportive activities. Final responsible for release of goods.
Job Responsibilities
1) Quality Strategy
⦁ Develop and implement the strategy related to the quality assurance of the materials, components and products. Ensure that proper control systems are applied on materials, components and products to guarantee at all times a safe and defect-free product to the patient.
⦁ Control and follow-up of internal GMP to secure the compliance to the internal requirements and the external regulations in all stages of the process.
2) Interactions:
⦁ Sales and Marketing:
⦁ Provide quality related information to customers via the sales and marketing department and via customer audits.
⦁ Production:
⦁ Ensure customer and quality requirements are implemented and respected in all stages of the production process
⦁ Provide quality related support to production in case of deviations or projects
⦁ Suppliers
⦁ Performing supplier audits to ensure that selected suppliers can guarantee the required quality level
3) Training:
⦁ Coaching and development of the co-workers to ensure that competences, skills and know-how are optimal used and to ensure the good departmental working
⦁ Pro-actively provide information and training about the current quality requirements and GMP-rules to production-related departments.
⦁ Ensure yearly GMP-training for all production employees.
4) Deviation management:
Supervising the handling of product and process failures (internal and external) and the evaluation of the countermeasures developed on preventing reoccurrence.
⦁ Handling of product complaints of Terumo Europe Production customers with focus on root cause solving
⦁ Non-conformity handling
⦁ CAPA handling:
⦁ Trend analysis:
6) Document management:
⦁ Ensure compliance of Production procedures with the relevant standards by quality review and approval of the procedures.
7) Improvement:
⦁ Active stimulation of continuous improvement through daily interactions and set-up of improvements projects. Information and training of the organization about the quality requirements and GMP.
⦁ Review and approval of change control files (CoC, Mod Sheet, validation records,…) in line with the applicable procedures and standards.
Profile Description
1. Higher scientific degree : pharmacy, industrial engineer, bio-engineer
2. By preference experience within a medical device, pharmaceutical or life sciences production environment
3. Knowledge of quality systems (ISO-13485, 21 CFR Part 820)
4. Languages : Dutch, English
Offer
5. Working for Terumo means contributing to society through healthcare.
6. We offer an opportunity to work in a top performing team. An organisation where everyone is treated with respect. We strive to create a diverse, equal and inclusive work environment. We invest in our associates by offering a broad array of development opportunities.
7. Linked with our core value Care, Terumo allows a hybrid way of working, combining office with home-based work. For the Engineering team a regular presence in the office close to the manufacturing plant, combined with work at home is the guideline.
8. Terumo offers an attractive salary and benefits package. Besides meal vouchers, interesting insurances, 100% public transport reimbursement, you also have the possibility to lease an (e-)bike.
During your recruitment process, you’ll be able to have conversations with Simon Roelens as the hiring manager and other passionate Terumo associates.