Quality Assurance & Regulatory Affairs Manager

Company: LHH US
Location: New York City
Posted on: February 18, 2026

Job Description:

Job Description Job Description Quality Assurance Regulatory Affairs Manager Location: Manhattan, NY Employment Type: Full-Time, Hybrid (In-office Tuesday through Thursday) Salary: $110,000 - $125,000 based on experience. Comprehensive benefits package (medical, vision, dental, 401k) offered as well. About the Role The QA/RA Manager is responsible for ensuring product quality, regulatory compliance, and cross-functional alignment across a portfolio of consumer packaged goods in the personal care, consumer health, or adjacent categories. This role is well-suited to someone who thrives in a fast-growth, entrepreneurial environment and enjoys hands-on quality and regulatory work. Key Responsibilities Regulatory Affairs Manage regulatory activities for U.S. and Canadian markets, ensuring compliance with applicable FDA, Health Canada, and FTC requirements. Maintain regulatory databases and systems, including GUDID, FURLS, and ITACS, ensuring accurate and timely updates. Support product clearance, regulatory documentation, and 510(k) preparation and submission as needed. Partner cross-functionally to ensure compliant product claims and adherence to evolving regulatory standards. Quality Assurance Support and maintain quality management systems and processes across the product lifecycle. Coordinate and/or perform product testing activities and ensure proper documentation. Maintain quality records and ensure alignment between product testing, manufacturing partners, and internal teams. Contribute to continuous improvement initiatives and help enhance quality reliability. Cross-Functional Collaboration Communicate effectively with internal stakeholders including R&D, Operations, Marketing, and leadership teams. Help drive clarity and alignment across project teams to support compliant and timely product launches. Required Qualifications Bachelor's degree in Life Sciences, Chemistry, Engineering, or related field. 3-5 years of experience in Quality Assurance and/or Regulatory Affairs within medical devices, personal care, consumer health, or similar regulated categories. Strong working knowledge of applicable FDA, Health Canada, and FTC regulations. Hands-on experience with: GUDID & FURLS database maintenance, ITACS, Product testing & clearance, Quality management systems Regulatory documentation, including 510(k) submission preparation Ability to operate effectively in a lean, entrepreneurial, fast-growth environment. Excellent written and verbal communication skills, with proven cross-functional partnership abilities. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.lhh.com/us/en/candidate -privacy Pay Details: $110,000.00 to $125,000.00 per year Search managed by: Stephanie Catoggio Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.lhh.com/us/en/candidate -privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Keywords: LHH US, Hartford , Quality Assurance & Regulatory Affairs Manager, Science, Research & Development , New York City, Connecticut