QA Compliance Officer
- Antwerp
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
Responsibilities:
- Review of specific Quality Documentation related to operational activities (mAbs P2)
- Review of electronic batch records and logbooks in MES
- Review and release of master batch records
- Review of operational quality documentation: preventative maintenance programs, calibration specification sheets, drawings
- Assist, review and follow up of other related quality documentation: change controls; quality events, corrective work orders
- Inspections in the manufacturing plant
Background:
- Master in biochemistry, chemistry, bio-engineering, or related industry
- Pharmaceutical/Biopharmaceutical experience
- Knowledge of MES (Manufacturing Execution System) is a plus
- Dutch and English language
Please apply today for further information!
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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