JOB DESCRIPTION:
MAIN PURPOSE OF 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
Experience
Minimum 1 year
Note: This job description is not to be considered an exhaustive statement of duties, responsibilities or requirements and does not limit the assignment of additional duties for this role.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Supply Chain
DIVISION:
AVD Vascular
LOCATION:
Netherlands > Heerlen : Argonstraat 1
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Not Applicable
