• Syner-G BioPharma Group (Boston, MA)
    …information, visit www.Synergbiopharma.com (Syner-G is seeking both Process and Validation Engineering Candidates) PROCESS ENGINEER POSITION OVERVIEW : Syner-G is ... specifications, design & development of process parameters, and the commissioning/ validation of manufacturing processes for compliance with quality and regulatory… more
    HireLifeScience (11/04/25)
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  • Tris Pharma (Monmouth Junction, NJ)
    …and related pricing calculations and compliance requirementsStrong understanding of pharmaceutical contract terms, language, and provisions for ... the Business Process Outsourcing partner), and ensures operational excellence in contract administration, rebate validation , government pricing compliance, and… more
    HireLifeScience (12/09/25)
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  • Insmed Incorporated (NJ)
    …Internship Program is designed to give you more than just a glimpse into the pharmaceutical industry-it's a chance to make a real impact. Over the course of the ... opportunity to gain hands-on experience in a corporate environment in the pharmaceutical industry, receive mentoring from highly skilled professionals, and work on… more
    HireLifeScience (11/01/25)
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  • Associate Director of Validation

    Bristol Myers Squibb (Indianapolis, IN)
    …(>$10M). + Demonstrated understanding and hands-on experience with radiopharmaceutical or pharmaceutical validation systems and compliance. + Direct experience ... and external contractors. **Skills and Qualifications** + Strong knowledge of pharmaceutical validation practices, including cGMP and FDA/USP/OSHA regulatory… more
    Bristol Myers Squibb (12/14/25)
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  • Validation Engineer II

    PCI Pharma Services (Bedford, NH)
    …an array of well-defined validation activities in support of cGMP pharmaceutical /medical device contract manufacturing across multiple PCI facilities. + The ... of equipment qualification, process validation , or cleaning validation is acceptable; QA pharmaceutical experience also..., or cleaning validation is acceptable; QA pharmaceutical experience also preferred. + Validation experience… more
    PCI Pharma Services (11/25/25)
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  • Validation Engineer III

    PCI Pharma Services (Bedford, NH)
    …array of well-defined validation activities in support of cGMP pharmaceutical /medical device contract manufacturing across multiple PCI facilities. In ... Validation , QA, MFG, or Engineering. + Experience in pharmaceutical or biopharmaceutical environment in operations/engineering/manufacturing/quality environments. + Combination… more
    PCI Pharma Services (11/22/25)
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  • Validation Manager

    Astellas Pharma (Westborough, MA)
    ** Validation Manager** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and ... of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We… more
    Astellas Pharma (11/21/25)
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  • Senior Principal Validation Engineer

    Curia (Albuquerque, NM)
    …Science, Engineering, or relevant field with a minimum of fifteen (15) years validation experience in pharmaceutical validation or aseptic/sterile product ... the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30...Science, Engineering, or relevant field with thirteen (13) years validation experience in pharmaceutical validation more
    Curia (10/03/25)
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  • Director of Validation

    Jabil (Hunt Valley, MD)
    …globe. Job Summary: The Director of Validation will lead all validation activities across pharmaceutical and medical device manufacturing operations with a ... Director will also schedule the appropriate resources for assistance with validation , to meet the established production schedule, vendor/ contract activities in… more
    Jabil (12/11/25)
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  • Validation Analyst II

    Curia (Albuquerque, NM)
    Validation Analyst II, Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
    Curia (11/06/25)
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  • Sr. Quality Engineer, Validation

    Cardinal Health (Indianapolis, IN)
    …waste and inventory reductions. **_Responsibilities_** + Conducts & develops validation and qualification protocols, projects and studies supporting manufacturing ... facility start-up and operation. Validation documentation to ensure products are manufactured in accordance with cGMP, pharmaceutical regulatory agencies,… more
    Cardinal Health (11/18/25)
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  • Validation Engineer III

    AbbVie (Branchburg, NJ)
    …+ Qualification as QRM facilitator commensurate with responsibility. + May supervise contract validation resources in the timely completion of activities in ... to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes… more
    AbbVie (09/30/25)
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  • Surmasis Pharmaceutical - Director…

    Katecho (Des Moines, IA)
    …the day-to-day operations of the Quality Department functions of Surmasis as a Pharmaceutical Drug contract manufacturer. Products within the scope of the ... Surmasis Pharmaceutical - Director of Quality | M-F |...batch releases, change control and documentation, equipment and process validation , deviation investigations, SOPs, supplier management and regulatory interactions,… more
    Katecho (11/07/25)
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  • Sr. Validation Engineer

    PCI Pharma Services (Rockford, IL)
    …technical discipline; advanced degree preferred. + Minimum of 5-8 years of validation experience in the medical device, pharmaceutical , or biotech industry. ... to pioneer and shape the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality… more
    PCI Pharma Services (09/18/25)
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  • Senior Validation Project Lead

    PACIV (Indianapolis, IN)
    …control solutions and instrumentation, we serve clients in the life sciences, pharmaceutical , medical device, food & beverage, and utilities sectors, specializing in ... tailored to regulated environments. Join our Indianapolis, IN team as a Senior Validation Project Lead and take ownership of validation initiatives for major… more
    PACIV (12/03/25)
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  • Sr. Cleaning Validation Engineer II

    Gilead Sciences, Inc. (La Verne, CA)
    …including implementation of new projects. + Coordinates the activities of assigned validation and contract personnel, ensuring the quality of completed work. ... Contributes directly to the completion of projects through the development of validation schedules, project plans, master plans, validation protocols and reports… more
    Gilead Sciences, Inc. (11/22/25)
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  • Engineer, Validation Commissioning

    AbbVie (North Chicago, IL)
    …+ May have Qualification as QRM facilitator commensurate with responsibility. + Works with contract validation resources as part of a team in the timely ... to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes… more
    AbbVie (11/06/25)
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  • Validation Engineer II

    PACIV (Indianapolis, IN)
    …Writing, or Information Systems) + Minimum 8 years proven experience in validation documentation within regulated environments (eg, pharmaceutical , biotech, or ... Validation Engineer II PACIV stands for P rocess...and instrumentation, we serve clients in the life sciences, pharmaceutical , medical device, food & beverage, and utilities sectors,… more
    PACIV (11/07/25)
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  • Pharmaceutical QC Scientist I

    Actalent (Columbus, OH)
    Pharmaceutical Scientist I INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE ... to join our team, focusing on bench testing and analytical support for pharmaceutical product development. You will conduct chemical and physical analyses to aid in… more
    Actalent (12/03/25)
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  • Associate Research Scientist: LBA PK & ADA Method…

    ThermoFisher Scientific (Lawrenceville, NJ)
    …in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, ... the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. **Summary:** The… more
    ThermoFisher Scientific (09/18/25)
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