• Aequor (Thousand Oaks, CA)
    …of industry/regulatory trends for verification/validation Experience with combination product / medical device quality systems verification Strong process ... experience with proper training/ background in technical side/ mathematics. NOT LOOKING for quality lab/ bench top/ science work. The job seeker needs to be… more
    HireLifeScience (06/25/24)
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  • Merck & Co. (Rahway, NJ)
    …product performance test methods as needed in tech transfer or lifecycle.Experience with medical device development with understanding of Design Controls (21 CFR ... (FMEA, DFMEA).Liaises closely with other partner functions including QA ( Quality ), Analytical Sciences, CROs and others to support project...MDR, Medical Electrical Equipment - EN 60601, Medical Device Software Standard - IEC 62304,… more
    HireLifeScience (07/11/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    … advice to the CSPV and key business function and collaborate with RD and Medical Affairs Quality to provide clinical safety QA advise wherever necessary. Ensure ... Global Project Team, Safety Management Team, Clinical Safety and Pharmacovigilance Medical Affairs, Companion Diagnostics/ Device Laboratories Vendors/ CROs… more
    HireLifeScience (07/10/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …needed to achieve the full potential of the organization to deliver pharmaceutical and medical device products to patients with unmet medical needs and ... healthcare environment required.Must have experience working within Bio, Pharma, Medical Device , Vaccines, Diagnostics, Combinations Products, including… more
    HireLifeScience (06/28/24)
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  • Eisai, Inc (Exton, PA)
    At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... Plant automation, Lab PCs and process and execution for lab workflow on device attached systems.Partner with Lab Operations, facilities in planning changes to the… more
    HireLifeScience (06/21/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
    HireLifeScience (07/13/24)
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  • Aequor (Devers, TX)
    …Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical testing is highly desirable. Extensive knowledge ... Mon - Fri, First shift (8:30AM - 5PM)Job Description/ Responsibilities: Provides Quality Assurance (QA) support to Devens Site and reporting Manger through … more
    HireLifeScience (07/10/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …requirements. This position has experience working on Phase I-IV studies within the medical device and/or pharmaceutical industry within one or more therapeutic ... collaborating with CROs and other vendors to ensure high quality deliverables are on time and within budget to...data management and/or related industry work experience in a medical device , pharmaceutical company, or similar environment… more
    HireLifeScience (06/05/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (06/29/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …preferred Experience Qualifications4 or More Years in pharmaceutical, biological and/or medical device operations including first-hand knowledge of drug ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (06/22/24)
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  • Exela Pharma Sciences, LLC (Lenoir, NC)
    …and quality and regulatory requirements important to pharmaceutical and medical device manufacturing labs.Able to write detailed investigation summary memos ... of laboratory documentation.Help with the implementation and interpretation of applicable quality and regulatory requirements (eg, FDA, GLP, QSR, cGMP, USP, and… more
    HireLifeScience (06/21/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (06/28/24)
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  • Providence (Missoula, MT)
    …a service line within Providence serving patients across seven states with quality , compassionate, coordinated care. Collectively, our medical groups and ... Description Provides direct quality care for cardiac patients in outpatient &...valued - they're invaluable. Join our team at Providence Medical Group Montana and thrive in our culture of… more
    JobGet (07/14/24)
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  • Eisai, Inc (Nutley, NJ)
    At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... surveys. Works with Procurement to select and implement vendor partners and device procurement.Builds and maintains a network of help desk knowledge management… more
    HireLifeScience (06/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …drug development and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred- 4 or More Years Experience in ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (05/17/24)
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  • US AMR-Jones Lang LaSalle Americas, Inc. (Kendall Square, MA)
    …knowledge and experience in a regulated GxP environment such as the pharmaceutical, medical device , or other life science industry. Required Skills and ... and tenant urgent requests. Supervises contractors working at the facility for quality workmanship. Performs all work in a neat, orderly, professional manner.… more
    JobGet (07/13/24)
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  • Medical Device Quality

    Randstad US (Brentwood, NY)
    medical device quality inspector. + brentwood , new york + posted june 26, 2024 **job details** summary + $25 - $35 per hour + temp to perm + no requirements ... our team. The successful candidates will be responsible for ensuring that all medical devices manufactured meet our stringent quality standards and regulatory… more
    Randstad US (06/27/24)
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  • Sr. Design Quality Engineer…

    Regeneron Pharmaceuticals (East Greenbush, NY)
    We are currently looking to fill a Medical Device Quality Engineer position. This position will provide Quality Assurance oversight and ensure compliance ... subject area and the following amount of work experience in combination device or medical device industry for each level: + Quality Engineer: 2+ years… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Medical Device Quality

    Kelly Services (Santa Rosa, CA)
    …Assurance Engineer_** _for a long-term engagement at one of our_ **_Global Medical Device Manufacturing_** _clients located in_ **_Santa Rosa, CA_** _._ ... _Our client_ _is a clinical-stage medical device company advancing transseptal left atrial...on a daily basis by developing, establishing, and maintaining quality engineering methodologies, systems, and practices. This position will… more
    Kelly Services (06/26/24)
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  • Senior Manager, Quality Engineering…

    ICU Medical (San Diego, CA)
    Device Software position manages the Quality activities related to ICU Medical Device Software Development, Testing, and Release, within Device ... considered the organization's expert within a particular discipline .Working knowledge of Medical Device Regulations . Quality compliance, audit, and… more
    ICU Medical (06/19/24)
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