Senior Manager QC Bioanalytics – Limerick

  • Reference: GY46098
  • Job Type: Permanent
  • Location: Limerick
  • Category: Science, Pharmaceutical & Food

Oversees the laboratory quality control testing of in-process, stability, and final drug products. Has technical responsibility for all bioanalytical aspects of QC testing. 

Responsibilities:

  • Coordinates with members of Manufacturing, Stability, and Business Ops to provide analytical support.
  • Manages QC Analysts, distributes work load, and monitors progress.
  • Oversees product testing to ensure efficient and compliant operations.
  • Reviews test reports.
  • Ensures QC Analysts receive proper training.
  • Attends meetings to keep informed of manufacturing priorities.
  • Ensures that safety standards are maintained.
  • Ensures compliance with applicable cGMP regulations and SOPs.
  • Investigates atypical and OOS test results as necessary.
  • Manage assay transfer internally from R&D to the QC laboratory or from PAS to the QC Laboratory.
  • Manage assay transfer externally from QC laboratory to contract labs, includes audits if needed.
  • Oversee QC projects including analytical commitments for Regulatory filing, follow-up actions for general GMP inspections and its readiness. 
  • Track and coordinate major analytical investigation 
  • Track and monitor timeline of analytical validation projects.
  • Monitor the team performance for Compliance events, track, assist and organize continuous improvement event.  
  • Interact with Regulatory Agencies as needed to ensure cGMP compliance.
  • Special projects as assigned.
  • Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations

Skills, Education & Experience:

  • BS in chemistry, biology or related field with 8+ years’ relevant experience (pharmaceutical or biotechnology industry) in laboratory management and analytical sciences
  • 5+ years’ experience in a supervisory/leadership capacity.
  • Thorough understanding of bioanalytical techniques in a cGMP environment. 

For a confidential discussion and more information on the role/company please email your CV to: amy.oneill@collinsmcnicholas.ie


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Amy O’Neill

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