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Quality/Clinical/Regulatory Affairs Senior

Job Title: Quality/Clinical/Regulatory Affairs Senior
Contract Type: Contract
Location: Elstree, England
Industry:
Salary: £30 - £35 per hour
Start Date: 2019-07-10
Reference: BH-108127
Contact Name: Amy Lindsell
Contact Email: Amy.Linsdell@nesgt.com
Job Published: July 17, 2019 17:31

Job Description

Program Manager Quality/Clinical/Regulatory Affairs Senior - FTC 12 months - Medical Devices

An exciting opportunity with one of the top Biotechnology companies in the world.

The organisation is seeking a full-time contract position based in their Hertfordshire Office.

Role/Description

This position is responsible for supporting the activities of the Design Owning Organization (DOO) at the Hertfordshire, UK facility.

The candidate will work with the Plants 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 Plants DOO.

Key Tasks

  • Support the PDO in fulfilling requirements for regulatory compliance, design control and risk management activities for Orthobiologic products manufactured at Hertfordshire
  • 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 Hertfordshire products
  • Generate and manage work flow 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
Key Skills

  • 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
Please apply online.