Are you interested in biopharmaceutical quality and advanced therapies? We are looking for Specialist to join our Quality Assurance team.

Your main task is to ensure the manufacturing operations in FinVector are conducted according to GMP and regulatory requirements by reviewing and approving GMP documents. The focus is on the QA review of BMRs, testing records, deviations, GMP project documents and risk assessments. You will also be involved with solving manufacturing, testing and quality system related problems.

In order to succeed you need to have a degree in biosciences or related. Moreover, understanding of quality systems and GMP-regulations as well as previous experience in pharmaceutical quality assurance are seen a plus but not mandatory. If you pay precise attention to details but you also easily manage entireties, this job suits you. Furthermore, we hope your way of working is systematic, unprompted and cooperative. All our documentation is in English and the team is international hence, you need to communicate fluently both in written and spoken English.

We offer you an active and lively work community with highly skilled and experienced colleagues in gene therapy manufacturing. We provide you an extensive occupational health-care and we support your well-being by ePassi-account. Our comprehensive initial training gives you a gentle start for your FinVector- career. Furthermore, we will continue to support your personal development.

The position is permanent and we hope that you are able to start to work at latest in January.

Apply by 29.10.2021!

For more information about the position, phone Miia Taavitsainen, Team Lead, QA Operations tel. +358 44 430 4682. You will reach Miia on weekdays between 10-16.

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