Associate Jobs in Neuenburg
LHH
Neuchâtel, NE
Your responsibilities : · Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation. Your profile : · Bachelors Degree in Engineering (Biomedical, mechanical, chemical, or electrical) or Science (Biology, Chemistry).
Integra Lifesciences Switzerland SAS
Le Locle, NE
Work order closing and analyze daily inventory transactions; explain manufacturing variances by reviewing work orders, and work with production supervisors to understand manufacturing yield. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily: Responsible for producing the monthly financial accounting package (within the Corporate published deadlines), including manufacturing KPI’s according to US GAAP rules.
NEXANS SUISSE SA
Cortaillod, NE
Reporting to the HVA engineering manager, the project engineer will be responsible of the HV accessories engineering for all types of High Voltage Cable Onshore Projects. The project engineer will be a part of the engineering team and will work in close coordination with the Tendering and Execution Departments locally and internationally.
Bristol Myers Squibb
Boudry, undefined
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, thi...
Bristol Myers Squibb
Boudry, undefined
L’Associate Operator, GMP Cleaning aura pour mission de réaliser les nettoyages des salles de la zone de production, des laboratoires et des salles d’échantillonnage, ainsi que le nettoyage de pièce d’équipement des différentes lignes de production et de conditionnement. Annoncer les situations dangereuses, les presqu’accidents/incidents et les accidents qui pourraient survenir sur le site auprès de son responsable direct et auprès du département EHS.
Bristol Myers Squibb
Boudry, undefined
QA Operations team is committed to actively support Celgene/BMS Boudry manufacturing site and other departments to ensure cGMP compliant production, testing and release of product on the Boudry manufacturing site. Ensure (and lead if necessary) that the initial quality assessment is completed in a timely manner according to requirements, support investigators , assess the criticality, review and approve the deviations, related CAPA and effectiveness checks.
Bristol Myers Squibb
Boudry, undefined
This team is responsible for the management of all QC samples (from receipt to destruction), visual testing of samples, preliminary investigations on samples associated with product complaints, stock management and ordering of consumables and laboratory equipment, support activities for QC department and activity related to incoming testing packaging. Finally, the QC Specialist Incoming is supporting activities related to the Pharmacopeial compendial review for packaging, evaluates impact of compendial changes on applicable QC procedures, handles associated change controls and manages Raw material sampling activities (including full and reduce testing).
Bristol Myers Squibb
Boudry, undefined
L’Associate Operator, GMP Cleaning aura pour mission de réaliser les nettoyages des salles de la zone de production, des laboratoires et des salles d’échantillonnage, ainsi que le nettoyage de pièce d’équipement des différentes lignes de production et de conditionnement. Annoncer les situations dangereuses, les presqu’accidents/incidents et les accidents qui pourraient survenir sur le site auprès de son responsable direct et auprès du département EHS.
Bristol Myers Squibb
Boudry, undefined
This team is responsible for the management of all QC samples (from receipt to destruction), visual testing of samples, preliminary investigations on samples associated with product complaints, stock management and ordering of consumables and laboratory equipment, support activities for QC department and activity related to incoming testing packaging. Finally, the QC Specialist Incoming is supporting activities related to the Pharmacopeial compendial review for packaging, evaluates impact of compendial changes on applicable QC procedures, handles associated change controls and manages Raw material sampling activities (including full and reduce testing).
Bristol Myers Squibb
Boudry, undefined
QA Operations team is committed to actively support Celgene/BMS Boudry manufacturing site and other departments to ensure cGMP compliant production, testing and release of product on the Boudry manufacturing site. Ensure (and lead if necessary) that the initial quality assessment is completed in a timely manner according to requirements, support investigators , assess the criticality, review and approve the deviations, related CAPA and effectiveness checks.
Bristol Myers Squibb
Boudry, undefined
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, thi...
Bristol Myers Squibb
Boudry, undefined
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, thi...
Bristol Myers Squibb
Boudry, undefined
Performs batch record review of commercial bulk product, semi-finished, and finished product batches manufactured, and prepare batch release documentation, using electronic MES platform. Special tasks can be assigned in crossfunctional projects/changes to support Boudry manufacturing site activities like new product introduction and launches.
Bristol Myers Squibb
Boudry, undefined
Performs batch record review of commercial bulk product, semi-finished, and finished product batches manufactured, and prepare batch release documentation, using electronic MES platform. Special tasks can be assigned in crossfunctional projects/changes to support Boudry manufacturing site activities like new product introduction and launches.
Bristol Myers Squibb
Boudry, undefined
Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, thi...