Work ScheduleFlex with On Call Duty Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE
Work ScheduleRotational shift nights/weekends Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed,
Work ScheduleRotational shift nights/weekends Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed,
Work ScheduleRotational shift nights/weekends Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed,
Work ScheduleRotational shift nights/weekends Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed,
Work ScheduleRotational shift days Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Loud Noises (Equipment/Machinery),
The Analytical Strategy Director is a key scientific and strategic leadership role. In this position you will be responsible for developing and driving analytical strategies that support drug discovery, development, and regulatory approval. The position ensures the
Overview Responsible for leading the successful operational execution of global, cross-functional Tech Ops projects of strategic importance to CSL’s product portfolio, ensuring delivery against defined scope, timelines, budget, and quality requirements. Main Responsibilities & Accountabilities Support
Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal
Principal Scientist, Pathogen Safety Support The Opportunity The Principal Scientist, Pathogen Safety Support provides scientific and operational expertise to support pathogen safety activities across manufacturing, technical operations, and product lifecycle management. This role partners closely with
Executive Director of Clinical Business Development - Strategic Accounts The Exec Director, Strategic BD is responsible for driving Enterprise-level sales growth through global account strategy, strategic partnerships, and long-term client engagement. This role focuses on identifying and
Opportunity To provide leadership and management to the Product Care & Artwork Management team. Responsible and accountable to enable geographical expansion by acting as the main interface to ComOps regions/markets regarding requests for launches and managing
# Senior Quality AssociateBewerbenlocations: EMEA, CH, Kanton Bern, Bern, CSL Behringtime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: R- Position Purpose The Senior Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers
Overview Position Purpose: The Senior Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product within the CSL Clinical Development portfolio. To do
Position Purpose The Senior Quality Associate is responsible for managing deviations, investigations, CAPAs, product technical complaints and change controls associated with development activities and manufacture of Investigational Medicinal Product within CSL Clinical Development portfolio. To do this, the