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

• Minimum 1 year

     

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