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QC Manager

  1. Ireland, Dublin
County Dublin
  1. Contract
Competitive
  1. Compliance / Quality Assurance
35183
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QC Manager - Contract - Life Sciences - County Dublin 

One of the top 10 best companies to work in Ireland is looking for QC Manager for their large-scale new facility in County Dublin. Is this you?

An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.

Responsibilities: 
  • Leadership of QC Shared Projects team to support manufacture, testing and release of Drug Substance and Sterile Drug Product
  • Responsible for the Site Trending Program for Quality Control
  • Responsible for delivering the QC Project portfolio in line with the overall QC Strategic Objectives
  • Responsible for delivering continuous improvement initiatives to facilitate ongoing cost saving and performance excellence
  • Develop a technical training structure and associated program to facilitate ongoing and consistent learning & development across the QC organization in line with the QC Network Strategy
  • Ensures audit readiness, both internal and external
  • Ensures the QC Projects Team operates in compliance with company policies and directives, evolving Health Authority regulations and expectations.
  • Builds and fosters strong relationships within the biologics quality and global quality network to drive compliance, strengthen quality systems and support company objectives.
  • Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to QC
  • Responsible for coaching, developing staff and completion of performance appraisal reviews.
  • Inspires transformative thinking and motivates employees to deliver benchmark performance.
  • Support QC planning and scheduling activities as required.

Requirements: 
  • A Bachelor/Masters in Science or Science related discipline and have a minimum of 6 years’ experience in the Pharmaceutical Industry.
  • Deep and demonstrated understanding and experience of the principles of GMP / GDP
  • An accomplished people manager with the ability to motivate and develop departmental staff through effective feedback and coaching
  • Proven success working well in a team environment, as well as proven leadership skills to manage a team of professionals through changing business needs.
  • Experience with interacting with regulatory agencies.
  • Knowledge of US and EMA GMP regulations and guidance.
  • Demonstrated leadership, interpersonal, communication, and motivation skills.
  • Demonstrated understanding of test methods and instrumentation associated with the testing of biopharmaceutical processes including chemistry and microbiological testing.
  • Planning and organizing skills are required to plan, execute and manage resources against timelines and project commitments; must be able to adjust to changing priorities and a dynamic work environment.
  • Strong leadership and people / project management abilities as well as proven decision making ability. Additionally, the successful candidate must be able to interact with a broad range of disciplines and exert positive influence within internal matrix teams across a variety of functions.

If this role is of interest to you, please apply now!


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