Stellenbeschreibungph3Company Description /h3 pEurofins Scientific is a leading international life sciences company providing a unique range of analytical testing services across multiple industries to make life and our environment safer, healthier, and more sustainable. From the food you eat to the water you drink and the medicines you rely on, Eurofins laboratories support many of the world’s largest companies in ensuring product safety, ingredient authenticity, and accurate labeling. /p pAs part of its commitment to society and the planet, Eurofins delivers testing services that protect public health while upholding strong corporate responsibility standards. This includes a dedicated focus on environmental sustainability as well as fostering diversity, equity, and inclusion across its global network. /p pEurofins BioPharma Product Testing offers complete CMC Testing Services for the Bio/Pharmaceutical industry, including all starting materials, process intermediates, drug substances, drug product, packaging, and manufacturing support through our broad technical expertise in Biochemistry, Molecular Cell Biology, Virology, Chemistry and Microbiology. /p pOur local presence ensures personal service backed by a unique global breadth of harmonised capabilities that support all functional areas of bio/pharmaceutical drug development and manufacturing, including method development, microbiology, process validation and quality control. /p h3Job Description /h3 pWe are looking for a QC Project Manager who will contribute to the significant growth of our business in Switzerland: /p ul liSupervision of customer projects with focus on Microbiology (including Environmental Utility Testing), as well as related subcontracted analytical services within the Eurofins Group /li liPlanning and organization of customer projects and related deliverables (e.g. review of technical documents, plans and validation reports) /li liMapping and configuration of projects in the LIMS system /li liEnsuring that the commissioned analytical work is carried out properly and on time, as well as co-responsibility for GMP‑compliant execution /li liApproval of analysis results and reports /li liSupervision and scientific support of ongoing customer projects and participation in the acquisition of new projects /li liProcessing laboratory deviations and root cause analyses (OOS) /li liCollaboration in the creation and preparation of quotations /li liGeneral process optimization and further development of the site /li liReview and revision of work instructions (SOPs) /li /ul h3Qualifications /h3 ul liCompleted studies in the field of life sciences (pharmacy, biochemistry, biology, ideally microbiology) /li liAt least 3 years of relevant professional experience in a regulated environment (ISO 17025, GLP, ideally GMP) /li liExperience in pharmaceutical quality control in the field of microbiology and clean water analysis /li liHigh customer and service orientation /li liVery good understanding of IT and Office applications, ideally experience with LIMS systems /li liIdeally experience in project management /li liYou are a team player, responsible and reliable /li liVery good German and good English skills /li liKnowledge of French is an advantage /li /ul /p #J-18808-Ljbffr
