- Sanofi (Framingham, MA)
- …science, or equivalent with at least 10 years relevant experience in the pharmaceutical, biotech, medical device or a related industry or at a Regulatory ... secure product launches and support compliance through audits, inspections, regulatory surveillance, and advocacy. Grounded in core values Integrity, Collaboration,… more
- Nesco Resource (Fall River, MA)
- …on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/ regulatory mandates and quality requirements. Complying with company policies and ... the Departmental SOPs. Reporting all issues that arise to the department head or reporting manager. Performing daily maintenance on equipment and machinery.… more
- Takeda Pharmaceutical Company Limited (Lexington, MA)
- …manufacturing operations and remain within their validated state and regulatory compliance.. The main manufacturing systems include incubators, bioreactors, ... 24/7 manufacturing operations and remain within their validated state and regulatory compliance. cause unknown with no product impact) complexity. Expectation to… more
- Merck (Boston, MA)
- …cross-functional impact, including drug device /combination products and software as medical device platforms. Reviews and resolves issues that span diverse ... Building, Human Resource Management, Immunoassays, Immunology, Immunotherapy, Management Process, Medical Devices , Mentoring Staff, Ophthalmology, Pathophysiology, People… more
- Sanofi Group (Cambridge, MA)
- …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... Care Combination Products, who in turn reports to the Head of GRA Device . The candidate will...to internal regulatory processes and procedures for medical devices and combination products. + Engage… more
- Sanofi Group (Framingham, MA)
- …with a minimum of 15 years relevant experience in the pharmaceutical, biotech, medical device , or related industries. + Extensive knowledge of Quality Systems ... **Job Title:** Compliance Head - US FDA **Location** : Framingham, MA, Morristown,...secure product launches and support compliance through audits, inspections, regulatory surveillance, and advocacy. Grounded in core values Integrity,… more
- Sanofi Group (Cambridge, MA)
- …or PhD in LifeScience; Law or Computer Sciences + **Pharmaceutical, biotech, medical device industry experience required** + Demonstrated experience in working ... **Job Title:** Head of Privacy, SpeCare and North America **Location:**...generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements,… more
- Sanofi Group (Cambridge, MA)
- …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... and direct reports. + In conjunction with the Sr. Director/Product Support Head , imparts senior regulatory guidance and advice during issues management… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …provide innovative technologies that make a meaningful difference in people's lives. Our medical devices , software and related services are used worldwide to ... experience in Indirect/Direct Strategic Sourcing. + Experience Consulting or in Medical Device Industry. + Supplier performance management, contract negotiation,… more
- Sanofi Group (Framingham, MA)
- …science, or equivalent with at least 10 years relevant experience in the pharmaceutical, biotech, medical device or a related industry or at a Regulatory ... secure product launches and support compliance through audits, inspections, regulatory surveillance, and advocacy. Grounded in core values Integrity, Collaboration,… more
