Scientific Researcher

1 month ago


Liverpool, Liverpool, United Kingdom Eurofins PSS Ireland Ltd Full time
Job Title: Commercial Scientist

We are seeking a highly skilled Commercial Scientist to join our team at Eurofins PSS Ireland Ltd.

Job Summary:

The Commercial Scientist will be responsible for ensuring the compliance and integrity of quality systems to maintain GMP and associated remedial activities. This will involve checking instrument calibration/service data, writing or updating reports, SOPs, and Calibration Protocols, and providing support for internal audits and regulatory inspections.

Key Responsibilities:
  1. Verify instrument calibration/service data for multiple analytical instruments/equipment, including HPLC, Dissolution equipment, KF, stability chambers, etc.
  2. Author and update reports, SOPs, and Calibration Protocols to ensure compliance with GMP and regulatory requirements.
  3. Support internal audits and regulatory inspections by providing documentation and evidence of quality systems.
  4. Collaborate with the team to ensure the client's requirements are fully met or exceeded.
  5. Identify opportunities for improvement of quality and service and implement continuous improvement initiatives.
  6. Work flexibly with multiple project teams as required.
  7. Support less experienced staff in techniques where the Scientist is competent.
  8. Attend meetings as required related to the scope of work.
  9. Stay up-to-date with technological advances in the area and adjust work as required with approval from the Lead Analyst.
Requirements:
  • A degree in a relevant scientific discipline such as pharmacy, pharmaceutical sciences, chemical engineering, or chemistry is required.
  • A sound, fundamental knowledge of analytical chemistry techniques is essential, with specific reference to the qualification and validation of analytical equipment in a GMP setting.
  • One to four years' relevant experience of pharmaceutical product analysis and/or manufacturing within a group organization.
  • Competent in authoring Quality documents based on templates, for example, Validation plans; Equipment Validation documents (URS, Third Party Protocol Approvals, Decommissioning documentation) would be beneficial.
  • Competent familiarity with scientific instrumentation and scientific applications.

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