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,
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,
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
Job Title The candidate will help the performance of operations in support of the manufacture of Commercial and Clinical Biologics. Work Schedule 10 hr shift/days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to
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
Sterile Processing Tech The Sterile Processing Tech position involves working in a surgical services environment. The shift is during the day, Monday through Friday, from 6:00 AM to 2:30 PM. The average daily tray volume is approximately 700.
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
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,
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
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,
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. The Impact You Will Make In a Clean Room environment, this role will be responsible
Manufacturing Excellence Operator Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together,
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
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