Work Schedule10 hr shift/days 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,
Quality Technician The Quality Technician is responsible for supporting site quality functions and ensuring compliance with applicable regulatory and quality standards, including ISO 13485, MDSAP, FDA, and EU MDR requirements. This role primarily supports aseptic manufacturing operations
Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world. Were driven by our mission to serve as a world-class, global CDMO that enables the
Downstream Processing Supervisor The supervisor is accountable for the success and oversight of downstream manufacturing processes. This includes conducting a variety of functions related to Downstream Biopharmaceutical Manufacturing such as large-scale chromatography, viral inactivation, viral filtration, ultrafiltration,
Job Title The candidate will help the performance of operations in support of the manufacture of Commercial and Clinical Biologics. Location/Division Specific Information: St. Louis, MO Thermo Fisher places a strong emphasis on employee development, fostering
Manufacturing Coordinator The Manufacturing Coordinator plays a critical role in supporting aseptic manufacturing operations through the coordination of production documentation, lot control, inventory reconciliation, and product release activities within a highly regulated cGMP environment. By partnering across
Work ScheduleSecond Shift (Afternoons) 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,
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Deviations Investigation Specialist partners with Operations, Quality, and cross-functional
Supervisor Production The Production Supervisor is responsible for the oversight of manufacturing operations associated with the manufacturing of radiopharmaceuticals which meet approved specifications by supervising from the floor, coaching and developing their team, and ensuring that
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Role Responsibilities Set up, tear down and change over all production machinery, as required. Perform
QA Technician At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make QA Technician provides Quality oversight of Operations (equipment and material preparation,
Senior Project Manager Curium is the worlds largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage
Manufacturing Technician Our client, a Life Sciences Biotech company, is looking for multiple Manufacturing Technicians for their St. Louis, MO location. Responsibilities: Set-up and operation of processing equipment such as Filter Integrity testing, Watson Marlow pumps, Autoclaves,
Manufacturing Technician Position Sirius Staffing is seeking candidates for a Manufacturing Technician position in St. Louis, MO. This is a temp-to-hire opportunity! Schedule: M-F, 2p-10:30p Pay: $23.00/hour + 7% Shift Differential Summary: The Manufacturing Technician is
Downstream Processing Lead Technician IV Work Schedule: Second Shift (Afternoons) Environmental Conditions: Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume,
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make In a Clean Room environment, this role will be responsible
Principal Project Manager This Principal Project Manager role provides a unique opportunity to collaborate across the different functions including Regulatory Affairs, Research and Development (R&D), Operations, Quality, Supply Chain, Finance, Legal, HR, Engineering, Marketing and Commercial.
Work ScheduleFlex 10 hr shift/days 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.
Description: Shift Hours: Monday Friday, 2:00pm 10:30pm Training will be on first shift: 6am-2:30pm Title: Manufacturing Technician 2 Temp to perm potential SAP experience 100% on-site Some college/Associates would be preferred Aseptic Technique experience Timeliness and punctuality