Quality Assurance Officer / Antwerpen / Fulltime / Temporary

Bedrijfsnaam: -
Plaatsingsdatum: 19/02/2019
Standplaats: -


SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Antwerpen Belgium.The CompanyThis company is specialized in blending and the primary packaging of pharmaceuticals powders. Within this company the strive for excellence results in the every day activities.

Role DescriptionAs a Quality Assurance Officer you will be responsible for the continuous monitoring of the quality of the batches. You will work together in a small team of professionals. Within this role you will work on the QMS, internal- and external audits and perform batch reviews. The role as Quality Assurance Officer will be temporary for a period of 6 months.

Responsibilities• Management and continuous improvement of the quality systems by correctly translating the processes into SOPs and keeping them up to date.
• Apply the quality guidelines by preparing and supervising external audits, but also carry out and follow up internal audits.
• Dealing with operational quality issues by acting as a point of contact for operations.
• Process and investigate incoming complaints.
• You report to the Quality Responsible and work in a day shift.

Requirements• Experience in Pharmaceutical Industry in a Quality role
• Knowledge of GMP regulations
• Knowledge of quality management systems
• Problem-solver
• Communicative
• Excellent written and spoken Dutch and English
• Be able to work individually and independently within a team

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.




Plaatsingsdatum :
Referentienummer :
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Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
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Werkervaring :
< 1 jaar (starter)
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