Are you a strong leader with experience in an operational environment? Do you want to play a key role in the production and logistics of vital clinical trial materials? Then you are the Supervisor we are looking for!
- 23 december 2025
- vacaturenummer: 721378
Salary depending on experience
Fulltime workweek, in dayshift
Learning environment
Fun and diverse team
Swalmen
Challenging role with responsibility
As Supervisor, your main task is to provide daily leadership and operational oversight for the on-site production teams. You will manage a team of approximately 25 employees, including temporary staff, and ensure that all workflows are executed safely, on time, and according to strict quality standards (SOPs)
- Coordinating the daily operations.
- Maintaining accurate inventory records, checking lot control, tracking expiration dates, and addressing any discrepancies.
- Working closely with the site Lead & Quality Assurance to prepare for audits, inspections, and ongoing compliance.
- Identifying operational issues, supporting root cause analysis, and implementing solutions
- Contributing to process improvement initiatives to enhance operational efficiency.
- Supporting the onboarding, cross-training, coaching, and ongoing development of your CTM staff.
- Maintaining clear communication between the floor teams and site leadership.
- Ensuring adherence to regulatory requirements and safety policies.
You are a committed, quality-focused leader who is comfortable working in a regulated environment.
- 5+ years of supervisory experience in a regulated operational setting
- Experience in Clinical Trial Materials (CTM), clinical trial operations, production, or logistics is a strong preference.
- Strong leadership capabilities to guide, coach, and motivate site personnel.
- The demonstrated ability to understand and apply SOPs, quality rules, and regulatory guidelines.
- Excellent organizational, prioritization, and problem-solving abilities.
- Strong interpersonal and communication skills to collaborate across on-site cross-functional teams.
- Proficiency in Microsoft Office and comfort using ERP or digital inventory systems.
- Effective English proficiency to read, interpret, and communicate operational and compliance-related information
This pharmaceutical services company plays an important role as a service provider for the testing of new medicines (clinical trials). They assist worldwide with tailor-made solutions. This includes arranging the logistics for all test materials and samples, and properly processing the data, in order to make the development of new medicines smoother and faster.
- A challenging and crucial role in a global company.
- The chance to lead and develop a team of professionals.
- A commitment to a safe, equitable, and inclusive workplace.
- Travel allowance of €0.23 per km
- Pension plan
Kun jij je helemaal vinden in deze vacature? Solliciteer dan snel!
Rody & Imke
Intercedenten
Vragen over deze vacature of functie? Bel of mail ons gerust even!
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