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QC Project Manager

  1. Dublin
  1. Contract
Competitive
  1. Compliance / Quality Assurance
05-02-2024
32800
QC Project Manager - Dublin - 2-Year Contract 

Would you like to grow your career, whilst contributing to scientific innovations that are transforming patients’ lives? Our client, a globally renowned biotechnology organisation, and voted one of the top 10 best companies to work for in Ireland, is looking to recruit a QC Project Manager to join their team.


Key Responsibilities: 

  • Overall responsibility for identifying, defining, scheduling, coordinating and driving to completion all Quality Control Projects within the remit of the Sterile Drug Product facility start-up operations.
  • Work with the QC Projects team to ensure the delivery of Method Transfer activities under the remit of the Sterile Drug Product Facility Start Up.
  • Compliance with all BMS Policies, Standard Operating Procedures and Registered Specifications.
  • Ensure the new laboratory within the Global Biologics Laboratory Building is set up to meet the needs of the new Sterile Drug Product Facility
  • Ensure the new GBL laboratory is set in a safe manner with Safety as a primary concern in its design.
  • Work closely with each of the QC teams to ensure they are informed of critical milestones, progress and support requirements.
  • Provide an effective and efficient QC Service to the Sterile Drug Product Project team through strong communication and focus of key priority milestones
  • Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
  • Review and Approval of project strategy reports, protocols and associated Project documentation.
  • Participate in regulatory agency inspections as required.
  • Strategically plan and implement procedures and systems to maximise operating efficiency through the use of Operational Excellence tools.

Key Requirements: 
  • Minimum of a BSc in Science or related discipline
  • Minimum of 8 years hands on experience in a GMP Laboratory Setting
  • >4 years Project Management / People Management experience
  • Strong background in Quality and Aseptic Manufacturing is required
  • Personal and Project management skills
  • Experience leading cross-functional teams
  • Knowledge of applicable regulatory requirements is desirable
  • Excellent written and verbal communication skills
If this role is of interest to you, please apply now! 
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