Quality Site Manager
SIRE Life Sciences®
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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 Utrecht Netherlands.
The CompanyWe are looking for a Quality Site Manager for a market leader in both development and production of labels for the pharmaceutical and food industry. The company has 4500 employees spread over three continents.
Role DescriptionAs a QA manager you will be responsible for everything involving quality on site. You will manage a team of 6 quality officer and a daily cycle involving deviations, complaints, following up on CAPA's en setting up and developing QMS (GMP, ISO9001, BRC) You will also be responsible for setting up and giving training to 40 full-time operators within the company.
Your daily cycle starts in the morning with determine what kind of actions have to be taken concerning deviations, after that you will analyze and continuously improve the quality management system, you will support in internal and external audits, you will be contact with customers and with our head office in France. You will be reporting to the Operations Manager and the Global Quality Manager
Responsibilities-Following up on complains and deviations (root cause analysis) + setting up CAPA's
-Daily management of 6 QAO (direct reports) and 40 operators (indirect reports)
-Managing and improving of the several Quality Systems (GMP, ISO9001, BRC)
-Organizing and giving training to operators
-Setting up continuous improvement projects (5why, 8D fishbone, FMEA)
-Accompany internal and external audits)
Requirements-Bachelor or Master in Life Sciences / Engineering
-At least 6 years of relevant work experience in a quality environment (experience in pharma is a plus)
-Knowledge of QMS (GMP, ISO9001,..)
-Experience in giving training, educating staff
-Experience in continuous improvement (5d, fishbone, 5why)
-Experience in project management (Lean six sigma) is a plus
-Experience in packaging is a big plus
-You are fluent in both Dutch and English
-You work proactively and are not afraid to work hard
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Greg Silberstein