Head of QC Services
Location: United KingdomSIRE® 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 and Biotechnology organisation, based in Cambridgeshire United Kingdom.
- You anticipate the weekly and monthly planning of laboratories and give the information on time analysis in accordance with the different services of the site.
- You coordinate and manage in-house analytical methods transfer activities with DA services, QA, RA and customers.
- Compliance with - cGMP standards and quality requirements, safety and environment are part of your requirements.
- You control investigations (OOS) and deviations, put in place the necessary corrective actions.
- You participate in internal and external audits.
- Significant experience in GMP environment
- Significant background in QC
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
The Company
Our client is a large international Pharmaceutical company based in CambridgeshireRole Description
Head of QC ServicesResponsibilities
- You have the responsibility of service and QC laboratories located on 2 plants of the site.- You anticipate the weekly and monthly planning of laboratories and give the information on time analysis in accordance with the different services of the site.
- You coordinate and manage in-house analytical methods transfer activities with DA services, QA, RA and customers.
- Compliance with - cGMP standards and quality requirements, safety and environment are part of your requirements.
- You control investigations (OOS) and deviations, put in place the necessary corrective actions.
- You participate in internal and external audits.
Requirements
- Education in related field- Significant experience in GMP environment
- Significant background in QC
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
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