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Senior Analyst

Thornshaw Recruitment
Start date
20 May 2024
Closing date
19 Jun 2024

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Quality, QC Analyst
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Job Details

On behalf of my client, a global pharmaceutical, we are collaborating with them on a new role for a Senior Analyst.   This is a permanent role with a 2-cycle shift.

Position Summary

Reporting to your Area Supervisor, conduct analysis as scheduled/requested by your supervisor and by making the best possible use of available resources.




Duties and Responsibilities


Key duties and responsibilities may include:






Conduct all tests, as instructed/scheduled by your area Supervisor, and in a timely manner. Be aware of the daily, weekly, and monthly KPI targets, schedule adherence requirements and Service level agreements (if applicable) of the area and of the importance of consistently achieving applicable targets. Assisting & performing (Leading) root cause problem solving exercises (e.g. 5 Why’s, Fish bone diagrams etc) as required. Troubleshooting of equipment as required in the event of issues. Host all Scheduling/Piloting Meetings in absence of Supervisor or as Designated. Review, check and update relevant documentation as necessary e.g. SOP’s, standard work, Methods/Specifications etc. Ensure all equipment in your area is within calibration. You are required to use and maintain it in the correct manner. Exercise good housekeeping and GLP practices daily by acting as a role model to your colleagues in terms of attitude, actions, garbing, wearing of PPE etc.

Work co-operatively and flexibly both within your department and with other departments. Be prepared to undertake additional tasks as requested to meet operational or business requirements. Contribute positively to the performance culture and effective operation of the laboratory.  


Position Requirements






Degree in Chemistry/Analytical Science/ Pharmaceutical Science or Forensic Science


  • Strong IT skills Strong attention to detail Demonstrate strong use of initiative/self-motivation and a disciplined approach. Good communication skills Strong positive attitude is essential for this position. Minimum of 3 Years Experience of working within a GMP Laboratory ideally within the Pharmaceutical or Biopharmaceutical Industry.





For additional information and full job spec email your CV to or call Tina at +353 1 2784701.  Thornshaw Scientific is a division of the CPL Group










Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission


For further details on our services contact Tina at +353 1 2784701 or email


Company info

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