475 regulatory manager jobs at 244 companies in Moosup, CT
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Regulatory Affairs Manager
Palm Beach Gardens or West Chester or Raynham or Oberdorf or Zuchwil
$117k-$201k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
6+ YOEBachelor's degree,6 years related experience in medical devices,knowledge of US/EU device regulations,RAC preferred,ability to manage regulatory submissions and teams,travel up to 10%.
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
6+ YOEBachelor's degree or equivalent,6+ years regulatory experience in medical devices,knowledge of US/EU regulations,RAC preferred,ability to lead teams and interact with regulatory agencies,travel up to 10%.
Waukegan or Hazelwood or Dublin or Illinois or Mansfield
$105k-$150k/yrHybridFull Time
Cardinal HealthNYSE: CAH: Distributes pharmaceuticals and manufactures medical products for healthcare providers.
7+ YOEBachelor's in science/engineering/life sciences required, 7+ years regulatory affairs medical device labeling experience, RAC preferred; deep knowledge of global device and environmental labeling regulations; strong attention to detail and project leadership.
Moneycorp: Provides global money transfer and foreign exchange services.
3+ YOE2+ MgmtOver 3 years in money transmitter licensing compliance, 5+ years in NMLS, 2+ years in management; strong knowledge of licensing regulations; English proficiency.
AcushnetNYSE: GOLF: Designs and manufactures high-performance golf products and apparel.
Bachelor's degree in a related field and extensive manufacturing compliance experience. Requires environmental permitting, remediation, hazardous materials, regulatory, risk management, leadership, and international compliance expertise.
Helen of TroyNASDAQ: HELE: Designs and markets branded consumer housewares and personal care products.
2+ YOEHigh school degree; 5+ years consumer-relations complaint handling or 2+ years regulatory adverse event reporting; familiarity with FDA/CPSC/MDR reporting, complaint management, SOPs, and audits; authorized to work in the U.S.
Project Manager - Regulatory, Audit and Compliance
Canton, Massachusetts, United States
$81k-$172k/yrHybridFull Time
CGINYSE: GIB: Provides information technology and business consulting services.
10+ YOERequires 10+ years of project or program management, process management and health insurance operations experience, healthcare payer regulatory expertise, strong stakeholder skills, and a bachelor's degree or equivalent experience.
Senior Regulatory Medical Writer, Client-embedded, FSP
Framingham or United States
$110k-$125k/yrRemoteFull Time
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
5+ YOEUS-based senior medical writer with 5+ years authoring clinical/regulatory documents; bachelor's in a scientific discipline required (advanced degree preferred); strong writing, project management, and regulatory knowledge.
Astellas PharmaTokyo Stock Exchange: 4503: Global developing and manufacturing pharmaceutical therapies for patients.
10+ YOEBS in Biology or equivalent, 10 years industry experience including 6 years in Regulatory Affairs or CMC regulatory work, global CMC expertise, health authority interaction experience, and fluent English.
OlympusTokyo Stock Exchange: 7733: Manufactures medical endoscopes and minimally invasive surgical tools.
15+ YOEBachelor's in a science-related field (Masters preferred), 15+ years regulatory affairs experience (10+ global preferred), global submissions and QMS experience, strong leadership, project management, and cross-functional skills.
Prin Regulatory Affairs Spec - Core Surgical innovations
Lafayette or Mansfield or Mounds View or North Haven or Boston
$120k-$180k/yrOnsiteFull Time
MedtronicNew York Stock Exchange: MDT: Develops and manufactures medical devices and digital health solutions.
5+ YOEBachelor's degree and 7+ years or advanced degree and 5+ years in regulatory affairs; medical device, FDA, EU, ISO, audits, submissions, leadership, and communication experience required.
FDA, Medical Device Directive (93/42/EEC), Medical Device Regulation (EU 2017/745), ISO 14971, ISO 13485, artificial intelligence, machine learning
Boston ScientificNYSE: BSX: Developer and manufacturer of innovative medical devices and therapies.
10+ YOEBachelor's degree, 10+ years medical device quality systems experience including audit program leadership; strong knowledge of ISO 13485, 21 CFR 820, EU MDR; inclusive leadership and stakeholder influence; ability to travel up to 25%.
Boston ScientificNYSE: BSX: Manufacturer of interventional medical devices and technologies.
10+ YOEBachelor's degree, 10+ years medical device quality systems experience including leading internal/external audit programs, strong knowledge of ISO 13485/21 CFR 820/EU MDR, global leadership, and ability to travel up to 25%.
ModernaNasdaq: MRNA: Develops and manufactures messenger RNA medicines and vaccines.
8+ YOEBS/MS/PhD in molecular biology, pharmaceutics, chemistry, chemical engineering or related field; 8+ years pharma/biotech experience; 5+ years regulatory CMC experience; strong knowledge of global CMC regulations and CTD format.
Executive Advisor, Enterprise Risk and Regulatory Affairs
Westborough, Massachusetts, United States
OnsiteFull Time
UMass Chan Medical School: Public medical school providing education and biomedical research.
10+ YOE5+ MgmtUndergraduate degree required; graduate degree (MBA or JD) preferred. 10+ years professional experience in health care, law, or government with 5+ years in leadership; deep regulatory, policy, contracting, and risk management expertise.
AVP for Behavioral Health Quality and Regulatory Affairs
Greenport, New York, United States
$120k-$140k/yrOnsiteFull Time
Stony Brook University: Provides public higher education, medical research, and healthcare services.
10+ YOEBachelor's in nursing or social work required; Master’s preferred within 5 years. Minimum 10 years combined clinical and administrative behavioral health experience. Experience with regulatory compliance, FMEA/RCA, risk management, data-driven quality improvement, and leadership.
Quality Safety Regulatory Project Manager, Hybrid, 40 hours, Days
Worcester, Massachusetts, United States
$87k-$157k/yrHybridFull Time
UMass Memorial Health: Provides integrated medical care and clinical research in Massachusetts.
5+ YOEMaster's in public health/healthcare/business (or bachelor's while enrolled in a master's), 5+ years related experience, quality/regulatory expertise, project management and data analysis skills, strong communication.
AbbVieNYSE: ABBV: Develops and sells innovative pharmaceutical and biopharmaceutical medicines.
15+ YOE5+ MgmtBachelor’s degree required; 15+ years in GMP pharmaceutical, biologics, or medical device manufacturing; 5+ years leading people; advanced cGMP/GXP knowledge and project leadership skills.
Global Regulatory Compliance Director (Marlborough, MA, US, 01752)
Marlborough or Arden Hills
$162k-$309k/yrHybridFull Time
Boston ScientificNYSE: BSX: Developing and manufacturing innovative medical devices for less-invasive treatments.
10+ YOEBachelor's degree, 10+ years medical device quality systems experience with audit program leadership, knowledge of ISO 13485/21 CFR 820/EU MDR, strong inclusive leadership, and ability to travel up to 25%.