Project Manager

Project Manager

Yourgene Health plc
Published
3rd December 2018
Location
Manchester, United Kingdom
Job Type

Description

Description of Role: Experienced Project Manager supporting Development, Operational and Commercial activities.

Overall responsibility: Ensure project objectives are accomplished by planning project activities, monitoring implementation and progress of projects.

Key areas of responsibility:

•    Develop detailed project plans to monitor and track progress, revise as appropriate to meet changing needs and requirements.
•    Establish and maintain relationships with third parties; supplies, collaborators, etc.
•    Co-ordinate internal resources and third parties for the high-quality execution of projects
•    Works closely with relevant stake holders to ensure effective and efficient implementation of the project(s)
•    Collaborates and coordinates across all the functional areas to ensure successful project completion
•    Support day-to-day operational aspects of the project(s) as required
•    Identify and minimize project risks
•    Identify and communicate project resource needs
•    Ensure that all projects are delivered on-time, within scope and within budget
•    Measure project performance using appropriate tools and techniques
•    Ensures project documents are complete, current, and appropriately stored.
•    Submits project status updates to stakeholders
•    Report and escalate issues to management promptly

Consults with:

•    Premaitha Health management and project team members, including (where appropriate) Project Leaders
•    Other Premaitha Health functions (e.g. Quality, Business Development, Legal, Finance, HR, Admin)
•    External consultants appointed by Premaitha Health
•    External companies (e.g., potential suppliers, commercial partners, etc.)

Supervisory/Management Responsibilities:

•    n.a.

Qualifications, Skills and Abilities:

•    Technical degree in engineering or science
•    5-10 years of relevant experience as a Project Manager.
•    Experience of working within a PMO
•    Enthusiasm, drive, thoroughness, diligence and a willingness to take personal responsibility to ensure that projects are successful
•    Excellent organizational skills with superb attention to detail and multi-tasking abilities
•    Excels when working to tight timelines
•    Excellent communication skills (written, verbal, formal presentation)
•    Strong interpersonal communication skills

Desirable Requirements:

•    Experience in the medical device industry or other regulated industry preferred
•    Experience with Medical Device compliant development methodologies (21 CFR 820, ISO13485)
•    Experience with IVD product

Please send in your CV and a covering letter explaining why you would be suitable for the role.

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