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!
what we offer ...job details
summary
- swalmen, limburg
- €4,244 per month
- temporary
- job categorywarehousing & distribution
job details
- 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!
Uiteraard staat deze vacature open voor iedereen die zich hierin herkent.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!
what we offer- 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!
Uiteraard staat deze vacature open voor iedereen die zich hierin herkent.experience
3qualifications
MBO
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