Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from
Perform proper handling of incoming product to insure accurate and available inventory. Perform all tasks according to best practice procedures. ESSENTIAL JOB FUNCTIONS Maintain safety standards while operating and identify unsafe practices and situations. Unload various
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
Job ID: 41577 | Location: Colton, California, USA | Work Model: Onsite Join Clariant and help shape the future of quality. In this role, youll champion quality throughout the product lifecycle by leading quality systems, driving
Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer
M-F, 6a-4:30pm (some flexibility), no holidays or weekends This position is responsible for collecting records, preparing and scanning records, performing quality control and validation of scanned documents. In addition, this position will include releasing medical records
We are seeking a talented Senior Data Engineer to join our Advanced Data Lake (ADL) team. This is an infrastructure-heavy, hybrid cloud role with Google Cloud Platform (GCP) as a core requirement. You will build and
Please use Google Chrome or Mozilla Firefox when accessing Candidate Home. By joining the American Red Cross you will touch millions of lives every year and experience the greatness of the human spirit at its best.
Date Posted:2026-07-14 Country:United States of America Location:US-CA-SAN DIMAS-936 ~ 936-960 Overland Ct ~ OVERLAND Position Role Type:Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to
Job Summary: Reporting directly to the University Registrar, the Associate Registrar is responsible for overseeing daily operations, directing and providing guidance in the planning, coordination, and assignment of tasks to the Records & Registration and Degree
Manufacturing Production Coordinator, Second Shift Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients lives accessible to as many people as possible. As a world
Quality Lead Join Clariant and help shape the future of quality. In this role, youll champion quality throughout the product lifecycle by leading quality systems, driving process improvements, supporting new product introductions, and ensuring compliance with
Quality Manager Gummy Dietary Supplement For over 60 years, MeriCal has been at the forefront of innovation in the dietary supplement industry, delivering custom manufacturing and packaging solutions with passion and precision. With state-of-the-art facilities in
Quality Assurance Manager Under the supervision of the Director of Quality Assurance this position is responsible for batch release for commercial product to the market. This position supports the activities and initiatives to implement and manage the Quality