Prep Mil Manager
PrepMilManager(fixedtermcontract-CDR)
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“Prep Mil Manager (fixed term contract - CDR) at Prep Mil Manager. Skills: Media preparation, Team leadership, Quality management. Lead and coach a team responsible for preparing. Ensure preparation records, labels and traceability meet GMP”
What You'll Achieve.
Protect quality and supply; Avoid delays; Meet testing schedules; Increase safety; Increase quality; Increase operational efficiency; Meet agreed timelines
Industry & Context.
Problem solvers; Investigations; Deviations; Corrective actions; Root cause analysis; CAPA
Fixed term contract, On-site presence required
What They're Looking For.
Must Have
Bachelor’s degree in chemistry, biochemistry, biology, pharmacy, bioengineering or related field, Minimum 5 years’ experience in a GMP laboratory environment, At least 2 years’ experience supervising or leading a small laboratory team, Knowledge of quality systems such as deviations, CAPA, change control and SOP management, Practical experience with laboratory equipment maintenance, calibration and qualification
Nice to Have
Master’s degree in a relevant scientific discipline, Experience preparing reagents and standards for analytical methods, Experience in regulated pharmaceutical or vaccine laboratory environments, Familiarity with laboratory computer systems and access/change control, Experience with continuous improvement tools (Lean, 5S or similar), French or Dutch language skills in addition to English
What You'll Do.
Lead and coach a team responsible for preparing
Ensure preparation records
labels and traceability meet GMP
Oversee equipment calibration
maintenance and laboratory readiness to
Plan capacity and priorities to meet testing schedules
deviations and corrective actions tied to
Drive continuous improvement projects to increase safety
Supervise daily media prep activity and assign tasks
Maintain and update standard operating procedures and batch
Verify material identity
storage and stability
Technical service and engineering to
Lead root cause analysis and CAPA for prep-related
Train staff on safe handling
documentation and quality
How You'll Work.
Team & Collaboration
QC lab teams; Quality assurance; Procurement; Technical services; QA; Technical service; Engineering
Full Job Description
# **This contract is a fixed term contract - CDR (Contrat de remplacement)** Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Position Summary You will manage the Media preparation team (Prep Mil) function in our Belgium Quality Control labs. You will lead a hands-on team that prepares media for routine and project testing. You will work closely with QC lab teams quality assurance, procurement and technical services to protect quality and supply. We value clear communicators, practical problem solvers and leaders who develop their people. This role offers visible impact, leadership growth and alignment with our mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: \- Lead and coach a team responsible for preparing media preparations. \- Ensure preparation records, labels and traceability meet GMP and site quality standards. \- Oversee equipment calibration, maintenance and laboratory readiness to avoid delays. \- Plan capacity and priorities to meet testing sc
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