- Integra LifeSciences (Boston, MA)
- …work experience is required. + A minimum of 2-4 years' experience in a medical device , pharmaceuticals, Quality / Regulatory Compliance, or other cGMP ... outcomes and set new standards of care. **ESSENTIAL DUTIES AND RESPONSIBILITIES:** The Quality Control Technician II will be responsible for performing quality … more
- Integra LifeSciences (Braintree, MA)
- …or related field preferred. + 5+ years GMP/GLP laboratory experience in a medical device , pharmaceuticals, Quality / Regulatory Compliance, or other ... Technician** will be responsible for supporting all activities in the Quality Control Microbiology team. This role also involves supporting non-conformance… more
- Integra LifeSciences (Braintree, MA)
- …a relevant scientific discipline. + A minimum of 2-4 years' experience in a medical device , pharmaceuticals, Quality / Regulatory Compliance, or other cGMP ... Technician II** will be responsible for performing environmental monitoring, quality control microbiological laboratory testing of in-process, finished goods,… more
- Sanofi Group (Cambridge, MA)
- …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... BS with 10 years regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory experience required. + At least… more
- Takeda Pharmaceuticals (Lexington, MA)
- …multidisciplinary teams to deliver device clinical outcomes that exceed quality benchmarks and regulatory standards. **Core Responsibilities:** ** Device ... liaison to Global Device Team, including engineering, regulatory affairs, quality , and commercial functions +...of experience** + Minimum 5 years of combination product, medical device , or pharmaceutical industry experience +… more
- Philips (Cambridge, MA)
- **R&D Development Engineer - Medical Device (Cambridge, MA)** In this role, you will contribute to a breakthrough cardiac ultrasound imaging solution that ... cardiac procedures. **Your role:** + Work on a collaborative, interdisciplinary, and experienced medical device R&D team, tasked with inventing and launching the… more
- Medtronic (Newton, MA)
- …and debugging software that interfaces with hardware components. Experience with regulatory compliance and security protocols specific to medical software ... user-friendly interfaces that enhance the usability and functionality of our advanced medical devices. The Senior Software Engineer will be a key player in… more
- Actalent (Boston, MA)
- …complex projects. Additional Skills & Qualifications + Additional certifications in clinical, regulatory , or quality fields. + Experience with venture capital, ... fundraising, and business development processes. + Experience designing or delivering clinical, regulatory , or quality training. + Experience setting up or… more
- Fresenius Medical Center (Lexington, MA)
- …regulations. * Maintains corporate regulatory files including EU technical files/documentation ( Medical Device Directives & Medical Device ... for NxStage Medical , Inc. products. Will provide regulatory input into key quality system processes...as a Regulatory Affairs Specialist in the medical device field or (ii) a Master's… more
- Hologic (Marlborough, MA)
- …science related field preferred. + A minimum of 8 years of experience in Regulatory Affairs within the Medical Device industry. + Experience ... with some complexity. + Demonstrated proficiency working within a QMS. + Firm understanding of regulatory challenges in the medical device or IVD space. +… more