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Contact Info
Ruth Holland
Life Science

01 507 9255
[email protected]
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Contract Manufacturing Manager

Reference:/RH/AWNI-683787 Location: Dublin South
Qualification:DiplomaExperience:5-7 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Project Manager

Life Science Recruitment are recruiting forContract Manufacturing Manager to join the team with our Pharmaceutical client based in South Dublin.

Member of a Work Cell within the Operations team to support the external Supply Network of Contract Manufacturing (ACM).


  • Support the Site Operations Manager in all aspects of the business to ensure on time delivery of all key products and projects, with key focus and ownership of Quality records including Deviation records, CAPA, CAPA EV, and Change Control records.

  • Active participation in Work Centre Team meetings with the contract site as well as internal site team, working collaboratively with the four pillars of Supply Chain, Quality, Operations and Process Development.

  • Project Management and Technology transfers when necessary: Follow-up and track activities in a department-wide project from conception to implementation and close-out. Manage timeline and highlight risks of transfer team activities; coordinate risk management activities as part of transfer; provide escalation to the right level.

  • Site performance monitoring: Report contract site performance metrics to site lead.
    Identify improvement opportunities for site performance; daily duties will include coordination, issuance, and review of meeting minutes, conclusions from analysis of data and metrics, continuous improvement and standardization of performance tools used by the Work Centre Teams (WCT), along with oversight and reporting of procurement/payment of invoices.

  • Manufacturing operations: Ensure accuracy and completion of data entries and/or tasks for budget development, monitoring, and reporting; inputs to contracts, confidentiality disclosure agreement(s), scope of work agreement(s), request for pricing/information, supply agreement(s) etc.
Education and Experience:
  • Bachelor’s in Business, Engineering or Science-related field
  • 5+ years of experience in DS, DP or packaging manufacturing environment, with preference for Pharma or Biopharma manufacturing (Drug Product) experience.
  • 5+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles
  • 2+ years of project management experience leading multi-functional and/or multi-location team
  • 1+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products
For more information contactRuth Hollandon087 7822 198or[email protected]