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Competences
The QC Lab Technician, GMP Cleaning will join the QC Sample Management team at Celgene Boudry.
The main responsibilities of the position will be to ensure the performance of cleaning activities on the furniture and the various premises of the Quality Control laboratory, the cleaning of the elements used during chemical analyzes (glassware in particular), the management of glassware stocks, the management of different waste and management of gowns. All in coordination with the different groups of the Quality Control department to ensure the activities.
The QC Cleaner can also participate in projects related to laboratory safety and continuous improvement, document scanning and archiving activities, as well as other activities intended for QC Management
Activities will be carried out in compliance, at all times, with laboratory procedures and safety rules (EHS) as well as following good documentation and manufacturing practices (GDP and GMP).
Skills/Knowledge Required
* Good knowledge of laboratory safety rules
* Knowledge of the environment and the operation of a quality control laboratory
* Ability to perform and document cleaning activities according to GDD and GMP rules
* Fluency in French
* Good collaboration and communication with members of QC and other departments
* Ability to work independently and collaborate within a team
* Available, flexible and careful in order to meet the different needs of the Laboratory Duties and Responsibilities
Duties and Responsabilities
Cleaning on the furniture and in the various premises of the QC laboratory
Management of the different types of waste generated by the activities of the QC Laboratory
Cleaning of elements used during chemical analyzes (glassware in particular) Inventory management and provision of clean elements used during chemical analyzes (glassware in particular)
Management of cleaning and the availability of laboratory coats
Cleaning of climatic chambers dedicated to Stability and of the Sampling booth
Realization and Documentation of activities carried out according to internal procedures in order to monitor operations
Maintenances on simple analytical equipment
Document scanning and archiving Reception of equipment for the laboratory
Participation and presentations at team meetings
Participation in projects and implementation of continuous improvement actions in the laboratory
Other responsibilities assigned by QC laboratory management
Comply with the directives and instructions defined in the quality system of our pharmaceutical site
Report dangerous situations, near misses / incidents and accidents that may occur on the site to their direct manager and to the EHS department
Participation in activities related to the management of Stability samples
Performing visual tests on samples
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Summit, NJ
Celgene Corporation, a biopharmaceutical company, discovers, develops, and commercializes therapies for the treatment of cancer and inflammatory diseases worldwide. It offers REVLIMID, an oral immunomodulatory drug for multiple myeloma (MM), myelodysplastic syndromes (MDS), and mantle cell lymphoma; POMALYST/IMNOVID to treat multiple myeloma; OTEZLA, a small-molecule inhibitor of phosphodiesterase 4 for psoriatic arthritis and psoriasis; and ABRAXANE to treat breast, non-small cell lung, pancreatic, and gastric cancers.
The company’s products also include IDHIFA for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (rrAML) with an isocitrate dehydrogenase-2 mutation; VIDAZA, a pyrimidine nucleoside analog for intermediate-2 and high-risk MDS, chronic myelomonocytic leukemia, and AML; THALOMID to treat patients with MM; and ISTODAX, an epigenetic modifier. Its preclinical and clinical-stage product candidates include small molecules, biologics, and cell therapies for immune-inflammatory diseases, myeloid diseases, epigenetics, protein homeostasis, and immuno-oncology.
The company has agreements with BeiGene, Ltd; Acceleron Pharma, Inc.; Agios Pharmaceuticals, Inc.; bluebird bio, Inc.; Lycera Corp.; Juno Therapeutics, Inc.; EXSCIENTIA LTD.; and IMIDomics SL, as well as immuno-oncology collaboration with Sutro Biopharma. Celgene Corporation was founded in 1980 and is headquartered in Summit, New Jersey.