Regulatory Specialist, Beauty & Wellness
Job in
Marlborough, Middlesex County, Massachusetts, 01752, USA
Listed on 2026-07-08
Listing for:
Helen-of-Tro
Full Time
position Listed on 2026-07-08
Job specializations:
-
Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Job Description & How to Apply Below
Look around your home, and you'll find us everywhere, in your kitchen, living room, bedroom, and bathroom. We are already making your everyday lives better. We are powered by knowledgeable, enthusiastic, and forward-thinking people committed to developing a culture of inclusion. Whether you are just starting your career or in need of a challenge, we recognize, develop, and empower talent!
Position:
Regulatory Specialist, Beauty and Wellness Department:
Regulatory for Wellness
Work Location:
Marlborough, MA Hybrid (work 3 days onsite)
Hybrid
Schedule:
At Helen of Troy, we embrace a flexible hybrid work model designed to support collaboration and productivity. For roles eligible for hybrid work, our standard schedule includes in-office collaboration from Tuesday through Thursday, with the option to work remotely on Mondays and Fridays. Any updates to this model will be communicated in advance. Please note that hybrid eligibility and schedules may vary based on business needs and manager expectations.
What you will be doing:
The role will be reporting to the Director – Regulatory & Clinical. The successful candidate will support in the coordination of effective regulatory strategies for Beauty & Wellness products, including ensuring we consistently meet applicable regulations across our global operations in regard to coordinating on the complaints and adverse event reporting process for all Medical and Wellness products.
Review all customer calls with a claim of a personal injury or property damage to determine if the adverse event needs to be reported to a regulatory body such as the FDA or CPSC.Determine if and potential adverse events/adverse events require a field action or CAPA to be taken on any given product line.
Coordinate the adverse event reporting process required to the respective regulatory agencies and brand licensors in the US in a timely manner for the Wellness products, both under the FDA and CPSC oversight.
Work with relevant international regulatory team members in Europe and Asia Pacific regions to determine if international adverse events shall be reported to the FDA.Manage the complaint investigation by driving and maintaining the individual complaint files for those complaints that need an investigation. Ensure that trend review, returns review and any other investigations are completed. Ensure complaint product is received and investigated through the complaint lab and the complaint is closed after investigation.
Assist in maintaining all SOPs and work instructions related to complaint management.
Perform other regulatory tasks as assigned including support FDA, ISO, other third-party audits; and any other internal audits related to complaints management, and regulatory related matters.
Skills needed to be successful in this role:
Familiarity with complaint handling processes and regulated reporting requirements across global regions.
Strong attention to detail.
Excellent verbal and written communication skills.
Minimum Qualifications:
High School Degree.
5+ years of experience in consumer relation’s complaint handling or 2+ years of experience in regulatory adverse event reporting of medical devices and/or consumer electronics.
Exposure to regulatory processes and software to facilitate compliance.
Ability to understand and interpret regulatory standards, such as medical device regulations (FDA, MDR, etc) and CPSC related and/similar regulations.
Good understanding of consumer relations call center workflows.
Authorized to work in the United States on a full-time basis.
Preferred Qualifications:
Associates or Bachelor’s Massachusetts, the standard base pay range for this role is $70,447. annually. This base pay range is specific to…
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