• Principal, Quality Assurance, GMP

    West Pharmaceutical Services (Exton, PA)
    …8 years of quality-related experience with preferred experience in pharmaceutical and/or medical device industry + Expertise of cGMP requirements, ISO standards ... **Job Summary** The Principal, Quality Assurance, GMP role focuses on ensuring compliance with cGMP standards within the WSS laboratories by identifying gaps,… more
    West Pharmaceutical Services (08/24/25)
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  • Consultant/Senior Consultant - Life Sciences…

    Guidehouse (Philadelphia, PA)
    …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... provides commercialization strategy and reimbursement services to pharmaceutical, biotechnology, medical device , and diagnostics companies. Our client services… more
    Guidehouse (08/10/25)
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  • Documentation Specialist

    Teleflex (Wyomissing, PA)
    …with product lifecycle management required to purchase, manufacture, and distribute medical device products. **Principal Responsibilities** * Serve as Change ... None **Requisition ID** :12631 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health… more
    Teleflex (08/19/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...held religious belief or other legally required exemption._ _In compliance with the ADA Amendments Act, should you have… more
    Fujifilm (07/24/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Harrisburg, PA)
    …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... deep understanding of business processes under GxP, ISO, and regulatory compliance Knowledge of Mfg. Process Controls...of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute… more
    Cognizant (07/18/25)
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  • Forklift Operator 2nd Shift

    Altium Packaging (Oil City, PA)
    …company's Good Manufacturing Practices. Essential Duties & Responsibilities: + Ensure compliance with corporate and plant safety standards and with applicable laws ... and regulations issued by regulatory agencies + Load trucks and secure product in...materials onto or off of pallets, skids, or lifting device + Monitor material usage on work floor and… more
    Altium Packaging (08/26/25)
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  • Senior Electrical Engineer

    WSP USA (Philadelphia, PA)
    …, and ensuring project work conforms with specifications, permit applications, compliance documentation, and regulatory and technical analysis memos. + ... the data integrity, documentation, procedures, training, monitoring systems, and record compliance and retention. + Interact with regulatory agencies,… more
    WSP USA (07/19/25)
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  • Scientist

    Kelly Services (Fort Washington, PA)
    …research and development efforts. + Maintain and operate analytical instruments, ensuring compliance with regulatory and safety standards. + Contribute to the ... in Fort Washington, PA. The role is eligible for medical benefits, paid time off including vacation (PTO), and...This role requires you provide your own IT (laptop) device The Scientist is tasked with carrying out method… more
    Kelly Services (08/28/25)
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  • Associate Director - Life Sciences Advisory…

    Guidehouse (Philadelphia, PA)
    …program design, implementation, and monitoring services to pharmaceutical, biotechnology, and medical device , companies. We support our clients across the ... in patient services programs, including Patient Services program design, PS regulatory / compliance issues, patient journey development particularly for… more
    Guidehouse (08/18/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Harrisburg, PA)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all… more
    Fujifilm (08/11/25)
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