49 job opportunities for validation protocols in United States updated today
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· Page 1 / 3Core Hours Sunday - Wednesday, 5:00 am - 5:30 pm Purpose and Scope The Aseptic Lead Operator supervises and leads processes including set-up and operation of processes related to supporting the injectable team, while ensuring that products are made with quality for our patients. Key Responsibilities
Canyon LabsCanyon Labs exists to raise the standard of services in the Medical Device and Pharmaceutical markets by providing streamlined and expert solutions in technical consulting, sterilization, analytical testing and packaging. We are committed to ensuring that quality services are delivered by meeting or
*Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts ( Nights 6p to 6a) on a 2-2-3 calendar rotation About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). T
This role will lead and execute manufacturing processing steps, associated activities, and assist the supervisor as required. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. Company Overview At FUJIFILM Biotechnologi
SMC Ltd.About Us: SMC Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, w
LillyAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and
EurofinsCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to
Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,0
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you re
Eli Lilly and CompanyAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and
Eckert & Ziegler Radiopharma IncVALIDATION SPECIALIST & PROJECT MANAGER (CONTRACT – 12–18 MONTHS) 🚀 Drive Validation & Expansion in Nuclear Medicine On-site – Wilmington, MA Local candidates only. Relocation not provided. Eckert & Ziegler Radiopharma, Inc. (EZRI) is expanding its U.S. radiopharmaceutical manufacturing operations,
Katalyst CROJob Summary We are seeking a Sr. Validation & Compliance Engineer to support commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilities within a regulated pharmaceutical/biotech manufacturing environment. The role involves developing and executing IQ/OQ/PQ
Katalyst CROJob Summary Quality Engineer II with experience in medical device manufacturing, process validation, and quality systems compliance within FDA-regulated and EU MDR environments. Skilled in IQ/OQ/PQ validation, process characterization, PFMEA, control plans, risk management, SOP development, and chan
Eckert & Ziegler Radiopharma IncVALIDATION SPECIALIST & PROJECT MANAGER 🚀 Drive Validation & Expansion in Nuclear Medicine On-site – Wilmington, MA Local candidates only. Relocation not provided. Eckert & Ziegler Radiopharma, Inc. (EZRI) is expanding its U.S. radiopharmaceutical manufacturing operations, including new production
IPG Medical Corporation is seeking a Software Quality Engineer in Marlborough, MA with the following requirements: Master's degree in Information Technology, Computer Science, or related field or foreign equivalent degree. 3 yrs of related experience. Required Skills: Manage and build high throughpu
Mark Cuban Cost Plus Drug Company, PBCCompany Description Mark Cuban Cost Plus Drug Company, PBC is transforming the pharmaceutical industry by offering medications at fixed, transparent profit margins, making affordable options accessible for patients affected by market and regulatory challenges. We are committed to addressing and elim
Algorithm Engineer Origin AI, an ADT Company Location: HQ / Hybrid About Us: Origin is redefining home security with TruShield℠ Security, a hardware-free, router-based solution powered by our exclusive AI Sensing℠ technology. TruShield goes beyond motion detection to deliver Verified Human Presence℠
Job Description This position follows a traditional 2-2-3 format from 6a-6P ( Black Day Shift) About This Role: The Manufacturing Lead performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGM
Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our
CAIA professional services company is seeking a Validation Engineer to ensure successful completion of commissioning and qualification activities in regulated pharmaceutical settings. The role involves developing documentation, writing protocols, and collaborating across teams. Candidates should posses
$40,000 – $63,000per year
Estimation confidence: Low
Estimate based on market data. Actual salaries may vary depending on experience, company, and location.
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