Eversource seeks an Associate Analyst, Transmission in Westwood, MA. This role supports regulatory filings, analyses, and coordination with ISO-NE, ensuring compliance with NERC and internal reporting standards. You will work with operations, planning, and engineering to facilitate timely filings and generate management-ready updates. Ideal candidates have 0–3 years of related experience, a Bachelor's in engineering or CS, and strong data/communication skills. #J-18808-Ljbffr
Transmission Regulatory Analyst (Hybrid) • Westwood, MA, United States
Now Hiring: Regulatory Compliance Manager | Food Manufacturing.Lowell, MA Full-Time Leadership Role | Food Manufacturing.Lead Regulatory Excellence at PGI Foods.Are you an experienced food industry... Show more
Dennis Partners is seeking a Regulatory Labeling Strategy Principal Consultant who will manage daily regulatory requirements for labeling strategies across client projects in the biotech and pharma... Show more
Work Your Magic with us! Start your next chapter and join EMD Serono.Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe lo... Show more
GlaxoSmithKline seeks an Associate Director Regulatory Affairs, Oncology in Massachusetts to develop and execute global/regional regulatory strategies for oncology assets, ensuring compliance with ... Show more
We are seeking a highly skilled Senior Business Analyst with deep expertise in U.IRS tax forms, brokerage or bank tax-reporting operations, and end-to-end tax filing workflows.The ideal candidate h... Show more
Determine and document change assessments for US Class II devices to ensure compliance with the US regulation.Plan and prepare submissions for US Class II devices, including creating, translating, ... Show more
Senior International Regulatory Affairs Specialist.NYSE: BFLY) is driving a digital revolution in ultrasound imaging and sensing with its proprietary Ultrasound-on-Chip semiconductor technology and... Show more
Associate Director or Director, Regulatory Affairs (Hybrid 3 Days In Office).The Associate Director or Director of Regulatory Affairs will be a key member of the STAT6 Regulatory team working in pa... Show more
Performs procedures for the general operation of the BSA/AML Program and its related activities to prevent illegal, unethical, or improper conduct.Performs the day-to-day operation of the BSA/AML P... Show more
Work Your Magic with us! Start your next chapter and join EMD Serono.Ready to explore, break barriers, and discover more? We know you've got big plans so do we! Our colleagues across the globe lov... Show more
Position Specific Requirements:.Responsible for internal, domestic, and international compliance activities working under the direction of the Regulatory Affairs Director.Assists the Regulatory Aff... Show more
Senior Associate Regulatory Operations.Lantheus is headquartered in Bedford, Massachusetts with offices in Canada, and Sweden.For more than 60 years, Lantheus has been instrumental in pioneering th... Show more
Regulatory Affairs Specialist IIThe Regulatory Affairs Specialist II supports the company's regulatory initiatives to meet strategic short- and long-term objectives.This includes assisting with the... Show more
Quanterix is a global leader in ultra-sensitive biomarker detection, enabling breakthroughs in disease research, diagnostics, and drug development.Its vision is to lead the next era of precision bi... Show more
MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications.Headquartered in Lowell, Massachusetts, MACOM has design centers and... Show more
Director, Global Regulatory Affairs.Stoke Therapeutics is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine.Using Stoke's propri... Show more
Director, Regulatory Operations.At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transfo... Show more
Cogent Biosciences is seeking an Associate Director, Quality Assurance GCP to provide strategic leadership over GCP quality activities across clinical development.This role ensures compliance with ... Show more
Director, Regulatory AffairsMapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders.We combine cutting-edge technologies includ... Show more
OverviewLeading complex medical device regulatory programs is no small task ” and this role owns it end‘to‘end.As the Principal Regul... Show more
