• Associate Director Production Quality

    Charles River Laboratories (Rockville, MD)
    …passionate about. **Job Summary** This position reports to the Site Head of Quality , and the person filling this role is responsible for partnering with functional ... stakeholders at the site level to ensure Quality performance and Compliance is designed into, and maintained,...+ Minimum 8 years of experience in a biologics, pharmaceutical , medical device, or related industry. 10 years of… more
    Charles River Laboratories (09/11/25)
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  • Quality Systems Specialist

    AbbVie (Mettawa, IL)
    …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Quality Systems Specialist is responsible for providing quality assurance ... support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of… more
    AbbVie (09/03/25)
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  • Director, Quality Operations

    Curia (Albuquerque, NM)
    Director, Quality Operations, Albuquerque, NM Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology ... 401k program + Learning platform + And more! Summary: The Director of Quality Operations oversees CGMP Quality Operations, including Incoming QA (IQA),… more
    Curia (08/23/25)
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  • Quality Program Manager II

    Curia (Albuquerque, NM)
    Quality Program Manager II, Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to...contributions + Learning platform + And more! Summary: The Quality Program Manager II is a key member of… more
    Curia (08/08/25)
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  • Quality Operations Specialist III

    Curia (Albuquerque, NM)
    Quality Operations Specialist III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development ... (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to...contributions + Learning platform + And more! Summary The Quality Operations Specialist III is an essential part of… more
    Curia (07/12/25)
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  • Supplier Compliance Manager

    Bristol Myers Squibb (Devens, MA)
    …record of successfully managing projects, and responsible for developing & implementing quality processes in a pharmaceutical environment. + Strong customer ... process with key stakeholders. + Lead global investigations in collaboration with Global Quality Supplier Leads, BMS Site Supplier Quality , and SQE teams. +… more
    Bristol Myers Squibb (09/16/25)
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  • Gen AI POD Captain

    Astellas Pharma (Northbrook, IL)
    …Compliance: + Familiarity with Good Practices (GxPs), regulatory requirements, and quality standards in the pharmaceutical industry. + Understanding of ... 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 (07/22/25)
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  • Manager, Quality Assurance - Onsite

    IQVIA (Durham, NC)
    We are seeking a ** Quality Assurance Manager to** join IQVIA Laboratories in **Durham, NC.** We hire passionate innovators who drive healthcare forward through ... we transform and accelerate research and development. As a Quality Assurance Manager, you will oversee and coordinate QA...Looking For:** + Bachelor's Degree preferred in life sciences, pharmaceutical sciences, or related field + Minimum 7 years… more
    IQVIA (09/25/25)
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  • Director, Quality & Regulatory Business…

    GE HealthCare (Chicago, IL)
    …**Job Description** **Roles and Responsibilities** + Executes against the Quality & Regulatory Business Development Process. This includes scheduling, preparation, ... formulation. + Impacts the team's ability to achieve service, quality , and timeliness of objectives. Work is subject to...of 7 years' experience in the medical device or pharmaceutical industry; or Bachelor's Degree and a minimum of… more
    GE HealthCare (09/13/25)
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  • Quality Control Analyst - 3rd Shift

    Hovione (East Windsor, NJ)
    …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... to: This position is for the 3rd shift: 9:30pm- 6:00am Defines and implements quality control techniques in order to verify the quality of raw materials,… more
    Hovione (09/07/25)
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