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Analytical Specialist I

  • Sector: Engineering
  • Contact Email: michelle.mcinerney@collinsmcnicholas.ie
  • Job Ref: 19167

Our client a major multinational based in Westport Mayo, are looking for an Analytical Specialist I to join their team. This is an initial 18 month contract.


The Role:

The Analytical Technology Specialist I in the Biologics Development Lab involves undertaking analysis of in-process, release, stability and investigational analytical activities. You will be responsible for the completion of write-ups in a timely manner and the review of other analysts work. You will be involved in supporting and executing Method Transfers, and Validation activities associated with biological drug product analytical processes. Other aspects of this role are QMS, compiling and review of Laboratory documentation (e.g. SOPs, methods, Master records, Batch Records, Reports) and carrying out routine lab tasks.


Responsibilities:

  • In process, release, stability and investigational analytical activities.
  • Support and execute Method Transfers, and Validation activities.
  • Compiling and review of Laboratory documentation.
  • Carry out training with new members of the group.
  • Support regulatory inspections as required.
  • Perform routine lab tasks to maintain a high standard of housekeeping.
  • Support laboratory projects to ensure timelines are maintained.
  • Ensure all testing is carried out in a timely manner to prevent late testing and delays in manufacturing schedule.
  • Participate at meetings and provide input to key projects to ensure completion.

Requirements:

  • Third level qualification in science-based discipline.
  • Lab experience desirable.
  • Good technical writing, communication, time management and organizational skills with a proven ability to use initiative when solving problems.
  • Understanding of GMP and experience with GMP regulatory inspections.
  • Understanding of aseptic practices in clean room environment.
  • Working knowledge of Quality Management System (QMS).
  • Understanding requirements of cross contamination controls in multi-product facility.
  • Experience with commercial and or clinical manufacture. 
  • Experience with interacting in project teams.
  • Flexibility of working hours may be required, and shift work may be required upon request.

For more information or a confidential discussion about this role please contact Michelle Mc Inerney.

michelle.mcinerney@collinsmcnicholas.ie

091 706 717