Contract

Program Manager Quality/Clinical/Regulatory Affairs Senior

SalaryCompetitive
LocationHertfordshire, United Kingdom
SectorMedical Technology

Description

Summary

This position is responsible for supporting the activities of the Design Owning Organization (DOO) at the required site. The candidate will work with the site Product Design Owner (PDO) in performing tasks related to regulatory compliance, change control, design control, and risk management for Advanced Surgery products produced under the site DOO.

Essential Duties and Responsibilities

  • Support the PDO in fulfilling requirements for regulatory compliance, design control and risk management activities for Orthobiologic products manufactured at site
  • Lead activities required in the design and development assurance and documentation to maintain regulatory compliance, particularly for the new European Medical Device Regulation (MDR).
  • Review and execute regulatory gap assessments against existing and new Regulation.
  • Maintain and remediate Design History Files and Risk Management files for products
  • Generate and manage workflow for appropriate change control documentation.
  • Project management of projects related to design assurance, risk management and DHF remediation.
  • Support the PDO in gathering information from Subject Matter Experts (SMEs) and technical resources for complaint investigations, change control, and regulatory submissions
  • Other tasks as needed

Qualifications

(To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.)    

  • Solid communication skills – both written and oral
  • Organizational skills and attention to detail
  • Ability to work effectively independently and in team environment.
  • Experience working in regulated industry (medical devices, drugs, biologics) is preferred.
  • Knowledge and experience working with medical device regulatory requirements, design control, change control, and risk management is highly desirable.

Education and/or Experience

  • Bachelor's degree in a scientific or engineering discipline with 1-5 years’ work experience or MS with 0-2 years’ experience
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