Regulatory Affairs Associate

  • Job ref:


  • Location:

    Trumbull, United States

  • Sector:

    Quality Engineers

  • Job type:


  • Contact:

    Dan Dubay

  • Published:

    9 months ago

  • Consultant:


For almost 50 years, Lighthouse Professional Services has worked to provide full-service consulting and staffing partnerships to clients in Connecticut, Massachusetts, Rhode Island, New Hampshire, and the Carolinas. Our innovative solutions can reach all areas within your firm including: Administrative, Information Technology, Engineering, Finance, Clerical and Light Industrial.

Lighthouse Professional Services committed to the success of the companies, candidates, and employees we serve. We invest in excellent working partnerships, powered by people.

We are currently seeking a Regulatory Affairs Associate in Trumbull, CT. to work a contract for a client.

Position Summary and Special Duties:

As a (an) your day-to-day duties will consist of and may not be limited to:

The Regulatory Affairs Associate will provide the internal regulatory affairs support for post-marketing of Class I, II and III medical devices. The incumbent will support the registrations and technical files projects for existing and acquired product lines. At the direction of the Sr. Director of Regulatory Affairs & Compliance, the Regulatory Affairs Associate monitors the regulatory environment and provides assessments of the impact of new and changing regulations.

Key Functions:

  • Identifies, completes, and files all necessary documentation as required with applicable Regulatory bodies, both domestic and international for product registrations.
  • Identifies, completes, and files all necessary documentation as required for site registrations both domestic and international locations.
  • Assembles, Reviews and updates “Technical Files” for existing and acquired products.
  • Prepares and updates “Declarations of Conformity” as per MDD.
  • Processes and updates CFGs.
  • Supports International Standards Organization implementation and maintenance.
  • Reviews Medical Device Regulatory standards and updates to ensure compliance.
  • Notifies Supervision and Management of Product safety issues.
  • Assists with maintaining and updating Order Entry Restrictions database.
  • Provides liaison with FDA, Notified Body, and Authorized European Reps.
  • Maintains collaborative relationship with R & D, Marketing and Operations is required.
  • Maintains collaborative relationships with external partners including regulators and external OEM suppliers.
  • Performs additional duties as required by management.


  • Bachelor’s Degree in Sciences, Engineering, Technical or equivalent.
  • Minimum 3-5 years quality, regulatory, compliance manufacturing, operations and/or engineering is required.
  • Command of Medical Device QSRs, ISO 13485, MDD 93/42/EEC, Canadian Regulations.
  • Three - Five years QA/RA experience in the medical device or related industry


  • MDD to EU MDR
  • Transfer Class 1 requirements
  • Tech documentation


  • Duration: 2.5-3 months contract
  • Location: Trumbull, CT.
  • Salary: contract role open to hourly rate based on experience
  • Can work remotely.  Some people come in 2 days a week as well.

Qualified candidates are encouraged to apply immediately!

Please include a clean copy of your resume and salary expectations and any references.