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 resolveproblems.
- 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
Required Experience:
IC
JOB DESCRIPTION:MAIN PURPOSE OF THE ROLEIndividual 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...
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 resolveproblems.
- 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
Required Experience:
IC
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