JOB DESCRIPTION:
MAIN PURPOSE OF THE ROLE
- Individual contributor with comprehensive knowledge in the specific area.
- Ability to execute highly complex or specialised work.
- Knowledge acquired from several years of experience or specialist training in particular area.
- Works independently, applies standards yet adapts precedent and may make departures from established processes to resolve problems.
- Packages, labels, assembles, and ships clinical supplies used in clinical trials in compliance with good manufacturing practices
- (GMP) regulations.
MAIN RESPONSIBILITIES
- Responsible to in-coming and out-going order processing and documentation, including generating delivery/shipping documents.
- Liaise with internal and external transport companies/departments for timely in-coming/ out-going shipments.
- Ensure prompt and accurate declaration of permits and prompt delivery and clearance of shipments.
- Investigate and action all non-conformance and recommend corrective actions.
- Responsible for records maintenance, protocol evaluation, coding of samples, and storage of approved materials.
- Maintains batch records and clinical supplies database.
- May have responsibility for manufacture of the active ingredients and dosage forms for clinical supplies.
QUALIFICATIONS
Education
- High School Diploma / GED
Experience/Background
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Supply Chain
DIVISION:
ANSC Nutrition Supply Chain
LOCATION:
Netherlands > Breda : Minervum 7201
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Not Applicable