Regulatory Affairs Associate needed

  • Job ref:


  • Location:

    Trumbull, Connecticut

  • Sector:

  • Job type:


  • Salary:

    depends on experience

  • Contact:

    Toby McAllister

  • Email:

  • Published:

    almost 2 years ago

  • Start date:


Lighthouse Professional Srevices is currently seeking a Regulatory Affairs Associate to work for a client in Trumbull, CT on a direct hire basis.

Position Summary:

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 of quality, regulatory, compliance manufacturing, operations and/or engineering is required
  • Command of Medical Device QSRs, ISO 13485, MDD 93/42/EEC, Canadian Regulations.
  • 3-5 years of QA/RA experience in the medical device or related industry.
  • Strong communication and problem solving skills.
  • Advanced computer skills.
  • Project organizational skills.

Additional Information:

  • 1st shift
  • Direct hire, salary range $75 -90K
  • Health insurance coverage, 401(k) and a defined pension plan, paid time off for vacation, personal, sick and holidays, as well as a wide range of other perks and benefits
  • Relocation assistance available

Monroe Staffing Services is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment and will not be discriminated against based on their race, color, Religion, gender, disability, veteran status, sexual orientation, gender identity, national origin or other protected classification.