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- job summary: A Packaging Lab Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This job conducts analytical testing to ensure compliance with cGMP regulations, prioritizing patient safety and product quality, while also providing support for process validations and adhering to quality system standards. location: Marlborough, Massachusetts job type: Contrajob summary: A Packaging Lab Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This job conducts analytical testing to ensure compliance with cGMP regulations, prioritizing patient safety and product quality, while also providing support for process validations and adhering to quality system standards. location: Marlborough, Massachusetts job type: Contra
- job summary: An R&D Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This role will work leveraging their subject matter experience to validate equipment and systems. They will collaborate with key stakeholders to help define needs and achievable solutions and/or justifications for equipment requirements and related validation. location: Marlborough, Massjob summary: An R&D Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This role will work leveraging their subject matter experience to validate equipment and systems. They will collaborate with key stakeholders to help define needs and achievable solutions and/or justifications for equipment requirements and related validation. location: Marlborough, Mass
- job summary: Your Responsibilities: As a core member of multiple new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory guidance (written and / or verbal) by owning the following tasks: 1. Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objectivejob summary: Your Responsibilities: As a core member of multiple new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory guidance (written and / or verbal) by owning the following tasks: 1. Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objective
- job summary: A major player in offshore wind projects is seeking a Quality, Health, Safety and Environmental Department Coordinator for it's project in Rhode Island. This project is set to last until the end of April 2025 with possible extension. As QHSE Coordinator, you will plan meetings, prepare reports, track deadlines, take meeting minutes, coordinate calendars across job sites, book travel, and oversee document storage. Candidates must be locajob summary: A major player in offshore wind projects is seeking a Quality, Health, Safety and Environmental Department Coordinator for it's project in Rhode Island. This project is set to last until the end of April 2025 with possible extension. As QHSE Coordinator, you will plan meetings, prepare reports, track deadlines, take meeting minutes, coordinate calendars across job sites, book travel, and oversee document storage. Candidates must be loca
