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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Quality Specialist


Reference:RK25901 Location: Dublin
Qualification:DegreeExperience:4-5 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QA Specialist

Quality Specialist
Shift - Days
RK25901
Contract 11 months
Dublin




We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



Key Responsibilities:

  • Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
  • Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures
  • Provides presence on the shop floor to support compliance and data integrity
  • Review and approve new and updated SOPs/ Work Instructions and Controlled Job Aides
  • Actively participates in the Tier process and uses this forum to make issues visible and to partner with the functional area on resolution
  • QA support, review and approval of Commissioning and Qualification lifecycle documents for capital projects and new equipment.
  • Will serve as the Quality SME for Performance qualification (PQ) activities across the site including but not limited to: Equipment, Facility and Utility PQ studies, Cleaning Validation, SIP, process validation
  • Participates as the quality member on cross functional projects
  • Support sustaining activities such as Change Management, Deviations, CAPAs, Equipment Requalification and Periodic review, Site Maintenance & Calibration Program
  • Provides support to internal audits and regulatory inspections
  • Collaborates with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans
  • Drive continuous improvement and utilise problem solving tools and Production Systems Participate in continuous improvement initiatives to enhance operational efficiency and resolve issues


Education and Experience:
  • 5 years of relevant post-degree work experience in GMP Manufacturing, Quality Assurance or Laboratory environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing or laboratory operations.
  • Bachelor degree, in a scientific or engineering field (preferred); candidates with degrees in other fields will be considered if accompanied by significant relevant experience
  • Understanding of QA operations an advantage as well as Regulatory agency engagement.
  • Experience working on manufacturing shop floor
  • Familiarity with GMP documentation review and/or shop floor auditing



If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.