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Trainer - Pharmaceutical Production
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Trainer - Pharmaceutical Production
Functieomschrijving
Our client is a global leader in the life sciences sector, focused on advancing innovative therapies and bio-manufacturing excellence. To strengthen their production organization, we are looking for an Operational Excellence Trainer. In this role, you will contribute directly to maintaining the highest standards in manufacturing and quality operations by developing, coordinating, and delivering technical training programs for production and quality personnel.
Job Description
As an Operational Excellence Trainer, you will be responsible for designing and delivering effective training sessions to ensure that all operators within manufacturing, production support, and quality control are equipped with the right knowledge and skills. You will oversee on-boarding programs for new employees, refresh existing staff through periodic retraining, and provide targeted coaching sessions following process changes or audit observations. Your goal is to create a learning culture that ensures compliance with Good Manufacturing Practices (GMP) and enhances overall operational performance. You will work closely with the Training Coordinator and the Head of Operational Excellence to track progress against training schedules, identify areas of improvement, and propose solutions to optimize training efficiency. In this hands-on role, you will frequently interact with production and quality teams, coordinating mock runs and practical equipment training sessions. Acting as a role model for GMP behavior, you help ensure that every process step meets both internal and external quality standards.
Responsibilities
- Plan, organize, and conduct on-boarding and recurring training programs for manufacturing, production support, and QC staff
- Deliver practical and classroom training sessions on GMP procedures, production activities, and process-specific operations
- Monitor training progress, maintain accurate training records, and report on adherence to the training schedule
- Identify training gaps, propose process improvements, and support the development of standardized training materials
- Coordinate and facilitate equipment and process training, including mock runs and hands-on sessions
- Provide instruction to contractors and visitors entering GMP-controlled areas
- Collaborate with aseptic trainers to uphold aseptic techniques and continuous improvement initiatives
- Act as a GMP ambassador, ensuring full compliance and promoting best practices across the organization
- Stay informed about updates in procedures, SOPs, and documentation to ensure alignment with current standards
Requirements
- Bachelor's degree in Life Sciences, Biotechnology, Biology, or a comparable technical field
- At least 3 years of experience in a GMP-regulated environment, ideally in manufacturing, training, or quality
- Proven experience in developing and delivering technical or compliance-related training programs
- Strong understanding of GMP principles and operational processes in a biotech or pharmaceutical setting
- Excellent communication and presentation skills in English; Dutch proficiency is an advantage
- Ability to engage, motivate, and coach staff with diverse backgrounds
- Hands-on attitude, structured working style, and attention to detail
- Comfortable working fully on-site in a high-compliance production environment
- Living in the vicinity of Limburg (NL), and in possession of a (European) working visa
Benefits
- Region: South Limburg (NL)
- Full-time on-site position within a state-of-the-art biomanufacturing facility
- Contract type: temporary assignment for 6 months with potential for extension
- Working hours: day shift, 40 hours per week
- Salary: Between €3500 and €5500 per month, based on experience
- Opportunity to contribute directly to life-changing therapies and scientific innovation
- Collaborative, international work environment with a strong focus on quality and professional growth
- Extensive learning opportunities through ongoing training programs and cross-functional collaboration
- Vacancy number: 26674
IMPORTANT NOTE: Unlimited EU working permit is required. Please do not apply if you do not have a working permit to live and work in the Netherlands or Belgium. If you do not have an unlimited permit, your application will not be processed.
Vacaturekenmerken
- Functie
- Trainer - Pharmaceutical Production
- Operational Excellence Trainer
- Technical Trainer
- Opleidingsfunctionaris (p&o)
- Training Coördinator
- Plaats
- Valkenburg
- Werkgever
- Oxford Global Resources
- Functiegroep
- HR / Training / Opleiding
- Branche
- Farmacie
- Provincie
- Limburg
- Uren
- Fulltime
- Dienstverband
- Tijdelijk
- Opleidingsniveau
- WO
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