QA Support Officer
at Eurofins Netherlands BioPharma Product Testing
2333 Leiden, Zuid-Holland, Netherlands -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 14 Sep, 2024 | Not Specified | 17 Jun, 2024 | N/A | Chemistry,Communication Skills,Gmp | No | No |
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Description:
Company Description
Eurofins PROXY is part of the internationally operating Eurofins Scientific. We are the largest Dutch GMP Quality Control laboratory for the pharmaceutical industry. Eurofins PROXY specializes in chemical and physical testing for (bio)pharmaceutical raw materials, intermediates and final products, and offers a very diverse package of analytical testing methods for national and international clients within the (bio)pharmaceutical industry.
Job Description
The Quality Assurance Support is mainly responsible for the administrative part within the department of QA Systems. The main tasks are the following:
- Archiving documentation according to GMP regulations;
- Sending and receiving documentation from the external archive;
- Electronic archiving of quality documentation in our LIMS system;
- Organizing and maintaining the GMP archive;
- Review and archive training documents;
- Distribution of logbooks and labjournals;
- Administrative support of the QA officers;
- Support during audits and inspections;
- Support in onboarding of new employees.
QUALIFICATIONS
- Completed HBO or MBO education, preferably in (bio)pharmaceutical sciences, chemistry or vocational laboratory training;
- An accurate and organized working attitude;
- Good communication skills, customer-oriented, team player, sense of responsibility;
- Good command of the English language spoken and written, command of the Dutch language is a plus;
- Experience working in a quality environment (GMP, GLP) is recommended;
- Available part-time for 24-32 hours a week;
- Located in the Netherlands and in possession of a valid work permit.
Additional Information
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Responsibilities:
- Archiving documentation according to GMP regulations;
- Sending and receiving documentation from the external archive;
- Electronic archiving of quality documentation in our LIMS system;
- Organizing and maintaining the GMP archive;
- Review and archive training documents;
- Distribution of logbooks and labjournals;
- Administrative support of the QA officers;
- Support during audits and inspections;
- Support in onboarding of new employees
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
2333 Leiden, Netherlands