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471 job opportunities

  • |  Posted On: Jul 01, 2026

    location: Gretna, LA 70053

    mode of work:On-siteOn-site

    duration: 6 Months, Contract

    The CAPA Process Analyst leads complex quality investigations, ensuring corrective actions are documented and compliant. Requires CAPA systems experience, a Bachelor's in Life Sciences, and ASQ CQA certification. Effective communication and technical writing are essential.

  • |  Posted On: Jul 13, 2026

    location: Durham, NC 27703

    mode of work:On-siteOn-site

    duration: 9 Months, Contract

    Mechanical Engineer with experience in CAD, SolidWorks, and automation systems. Responsible for designing mechanical components and systems, contributing to R&D teams, and developing cost-effective prototypes. Requires strong problem-solving and analytical skills, along with technical judgement and ...

  • |  Posted On: Jul 06, 2026

    location: Athens, GA 30601

    mode of work:On-siteOn-site

    duration: 6 Months, Contract

    Position as Principal Specialist in Packaging, focusing on training and compliance. Responsibilities include leading documentation teams, developing training programs, and ensuring regulatory compliance. Requires strong skills in packaging, documentation management, and training program development ...

  • |  Posted On: Jul 06, 2026

    location: Livermore, CA 94550

    mode of work:On-siteOn-site

    duration: 6 Months, Contract

    Role as Site Administrator involves managing office operations, ensuring efficient work environment, and engaging with employees and visitors. Requires strong organizational and communication skills, with experience in event planning. Ideal candidate is proactive, with a focus on employee ...

  • |  Posted On: Jul 06, 2026

    location: Union, NJ 07083

    mode of work:On-siteOn-site

    duration: 5 Months, Contract

    Looking for a Phlebotomist Floater to perform blood draws and manage specimen preparation across various locations. Requires 5 years of phlebotomy experience, strong phlebotomy skills, leadership abilities, and confidentiality. Must handle complex customer practices and collaborate with multiple ...

  • |  Posted On: Jul 13, 2026

    location: Santa Clara, CA 95054

    mode of work:On-siteOn-site

    duration: 12 Months, Contract

    Looking for a Regulatory Affairs Senior Specialist skilled in regulatory and quality systems management. Responsible for managing international addendum labeling activities, collaborating across functions, and leading complex labeling initiatives. Requires strong project management and stakeholder ...

  • |  Posted On: Jul 13, 2026

    location: Redmond, WA 98052

    mode of work:On-siteOn-site

    duration: 12 Months, Contract

    The Opto-Mechanical Engineer will lead mechanical engineering workstreams for sensor integration on wearable hardware, ensuring performance and reliability. Requires strong mechanical design skills, proficiency in 3D CAD modeling, and experience with NX CAD software. Responsible for developing ...

  • |  Posted On: Jul 01, 2026

    location: Bethlehem, PA 18017

    mode of work:On-siteOn-site

    duration: 12 Months, Contract

    The HR Shared Services Rep provides support in HR areas like Benefits, Payroll, and Colleague Relations while managing and improving processes. Key responsibilities include answering inquiries, facilitating training, and collaborating with stakeholders. Requires HR experience, Workday skills, and ...

  • |  Posted On: Jun 22, 2026

    location: Barceloneta, PR 00617

    mode of work:On-siteOn-site

    duration: 6 Months, Contract

    The QA Technician ensures the quality of pharmaceutical products and manufacturing processes. Key responsibilities include sampling, testing, documentation, and equipment checks. Requires GMP knowledge, bilingual skills, and proficiency in SAP and other systems. Work involves team collaboration in ...

  • |  Posted On: Jul 13, 2026

    location: Sylmar, CA 91342

    mode of work:On-siteOn-site

    duration: 6 Months, Contract

    Seeking a Regulatory Affairs Associate with experience in regulatory applications and medical devices. Key responsibilities include authoring PMA supplements, supporting EU MDR updates, and reviewing engineering protocols. Must possess knowledge of FDA PMA and EU MDR regulations. A degree in ...

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