Project Manager

Project Manager
  • £40,000 - £70,000 per Annum
  • Permanent
  • Windsor, Berkshire, England, UK Windsor Berkshire UK SL4 4AA
Job Ref: J2162554
Sector: Engineering
Sub-sector: Medical Devices
Date Added: 03 November 2021
Are you experienced in project management within the R&D medical device sphere? Would you like to join a growing medical device company? Apply now.

Project Manager

SRG are partnering with a global medical device company who specialise in high-value measurement and diagnostic instruments for the eye care industry. Our client is looking for an experienced Project manager within the medical device industry to join their R&D team. Offering a competitive salary and desirable benefits package.

Responsibilities include:

Project Management

  • Maintain project schedules by monitoring project progress, coordinating activities, identifying, and raising issues and proactively managing risks.
  • Monitor the project costs and keep these updated, identifying any risks to project budget early and raising these with the Head of Engineering.
  • Coordinate activities and resources required to deliver the project to agreed timelines, budget, and quality targets.
  • Monitor sub-contractors keeping track of whether the Keeler quality standards and deliverables are maintained, raising any issues with the R&D Manager.
  • Establish and maintain regular and effective communication with the Head of Engineering, in all activities required to design, develop, and deliver the product successfully.
  • Provide a weekly summary of each development project to the R&D manager as well as providing monthly status reports outlining project timeline, budget, and risks.
  • Control designs through a gated development process and associated decision making.
  • Make use of standard project management tools to keep track of people and progress.

Regulatory and QA/QC

  • Jointly responsible with Keeler Q&R for the successful implementation of an eQMS
  • Designing the R&D procedures and workflows that will be established in the eQMS system to ensure compliance to relevant regulations and quality standards are met and maintained.
  • Create and maintain all relevant project/product documentation (including Design History Files and Device Master Records) in line with company SOP's and national/international standards and regulations.


  • Minimum of 3 years proven industry experience in carrying out projects within the Medical Device Industry.
  • Relevant degree in a STEM subject or a proven track record in Project Management.
  • Working knowledge and practical experience with the quality and regulatory guidelines as they apply to Medical Devices.
  • Experience leading multiple projects with common resources /resource balancing.

To find out more information please contact Kyle Stevenson on the following details.

0161 868 2238

03/12/2021 12:20:08
GBP 40000.00 70000.00 Annum
Contact Consultant:
Kyle Stevenson

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