- BioLife Plasma Services (West Springfield, MA)
- …(in state of licensure) for basic IV therapy + Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist + Two years in ... a clinical or hospital setting **More about us:** ** ** At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and… more
- Nanobiosym, Inc. (Cambridge, MA)
- …update protocols and architecture. + Experience with medical device compliance and documentation as per FDA and ISO13485 standards + PhD or MS / ME in EECS What We ... Offer: + An innovative work environment tackling challenging embedded systems projects. + Opportunities for professional growth in secure firmware development and advanced embedded technologies. + Competitive salary and benefits package. more
- ManpowerGroup (Andover, MA)
- …and accuracy. + Keep work area clean and follow safety guidelines (OSHA, FDA , CDC). **What's Needed?** + 2+ years of mechanical or electromechanical assembly ... experience (preferred) + Comfortable working with small parts, wires, and reading diagrams + Able to follow instructions and communicate clearly + Must be able to lift up to 40lbs + Experience with SAP or Agile is a plus **What's in it for me?** + Free… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …+ Ensure the Sponsor-Investigator and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures, ... including DFCI CTO Monitoring standards and guidelines. + Adhere to the protocols' Data Safety Monitoring Plans; eg monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring tracking forms and other monitoring… more
- Stantec (Devens, MA)
- …environment with cross-functional teams. - Familiarity with GMP regulations, FDA standards, and validation protocols. - Experience supporting capital projects ... or facility upgrades in regulated environments. - Understanding of risk-based scheduling and project lifecycle in Life Sciences industry. Education and Experience - Bachelor's degree or equivalent in Engineering, Construction Management, Finance, Business, or… more
- Bayer (Cambridge, MA)
- …the Regenerative Medicine Advanced Therapy (RMAT) designation by the US Food & Drug Administration ( FDA ). The phase 1 data from this program was on the cover of the ... May 22nd, 2025 issue of Nature and is now conducting a Phase 3, registrational study. Successful commercialization of this asset provides an exciting challenge as we enter this new and important therapeutic area, The cell therapy space brings additional… more
- Stantec (Burlington, MA)
- …related to bio-pharmaceutical dosage forms, nutraceutical facilities and other regulated FDA or similar facilities where drug products are manufactured, stored in ... GMP conditions and distributed, including computerized and automated systems which require qualification and validation for compliance. The commissioning and validation of equipment, facilities, utility systems and computerized systems are intended to verify… more
- System One (Harvard, MA)
- …integrity principles + Proven attention to details + Comfortable working in an FDA regulated environment. System One, and its subsidiaries including Joule, ALTA IT ... Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued… more
- Mentor Technical Group (Boston, MA)
- …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six… more
- Chewy (Boston, MA)
- …Preventive Controls Qualified Individual (PCQI) training. + Working knowledge of FDA regulations, including 21 CFR Part 507.27 (Current Good Manufacturing Practice ... for Animal Food) and the Sanitary Transportation of Human and Animal Food rule. + Experience in e-commerce, retail, manufacturing, or startup environments. + Proficiency in SQL and Tableau for data analysis and visualization. + Background in packaging… more