Analytical Technology Specialist
TR/081293
Posted: 05/03/2026
- Competitive Salary
- Ireland, County Mayo, Westport
- Contract
Orion Group Life Sciences are currently recruiting an Analytical Technology Specialist on behalf of our Multinational Biopharmaceutical client based in Westport (Fully Onsite) on an initial 12-month contract.
This role is integral to supporting the NPI group's activities in release and stability testing for products in development. The specialist will perform Cell Based Potency Assay (CBPA) and ELISA testing for both development and clinical products generated by Biologics Development Manufacturing. Additional responsibilities include new method transfers, validations, and maintaining laboratory operational excellence. Previous experience in a cGMP/GLP environment is highly advantageous.
Responsibilities:
• Support NPI QC Testing on Primary Stability Batches, Clinical, Pre Performance Qualification, Demo, and investigational lots using Cell Based Potency Assay and ELISA methods
• Timely review of testing records and all associated documentation
• Conduct routine laboratory duties such as critical reagent qualifications, inventory management, and equipment maintenance
• Ensure all activities adhere to regulatory (QA and EHS) and corporate requirements
• Open and progress QMS records as needed (Laboratory Investigations, Change Controls)
• Complete assigned training in a timely manner
• Maintain laboratory data integrity by understanding applicable regulations and business processes
• Provide input on assay performance monitoring and trending
• Support Root Cause Analysis Investigations
• Participate in departmental and Tier meetings
Qualifications:
• Bachelor’s, Master’s, or Ph.D. in Biological Science with 1-3 years of QC GMP experience
• Practical experience in mammalian cell culture and basic techniques (passaging, freeze-down, drug treatments) is an advantage
• Strong scientific and practical understanding of ELISA-based methods • Proven problem-solving skills
• Clear communication skills
• Good organizational and interpersonal skills
• Willingness to up-skill and collaborate
• Ability to lead and drive projects to meet timelines
• Focus on Right First Time (RFT
People are our business worldwide
Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.
This role is integral to supporting the NPI group's activities in release and stability testing for products in development. The specialist will perform Cell Based Potency Assay (CBPA) and ELISA testing for both development and clinical products generated by Biologics Development Manufacturing. Additional responsibilities include new method transfers, validations, and maintaining laboratory operational excellence. Previous experience in a cGMP/GLP environment is highly advantageous.
Responsibilities:
• Support NPI QC Testing on Primary Stability Batches, Clinical, Pre Performance Qualification, Demo, and investigational lots using Cell Based Potency Assay and ELISA methods
• Timely review of testing records and all associated documentation
• Conduct routine laboratory duties such as critical reagent qualifications, inventory management, and equipment maintenance
• Ensure all activities adhere to regulatory (QA and EHS) and corporate requirements
• Open and progress QMS records as needed (Laboratory Investigations, Change Controls)
• Complete assigned training in a timely manner
• Maintain laboratory data integrity by understanding applicable regulations and business processes
• Provide input on assay performance monitoring and trending
• Support Root Cause Analysis Investigations
• Participate in departmental and Tier meetings
Qualifications:
• Bachelor’s, Master’s, or Ph.D. in Biological Science with 1-3 years of QC GMP experience
• Practical experience in mammalian cell culture and basic techniques (passaging, freeze-down, drug treatments) is an advantage
• Strong scientific and practical understanding of ELISA-based methods • Proven problem-solving skills
• Clear communication skills
• Good organizational and interpersonal skills
• Willingness to up-skill and collaborate
• Ability to lead and drive projects to meet timelines
• Focus on Right First Time (RFT
People are our business worldwide
Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.
Beatriz Olmedo
Lead Recruitment Consultant
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