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QC Stability Reviewer

Location: Dublin North, Dublin
Salary: Negotiable
Posted: 3 months ago
Role type: Permanent
Industry: Science, Technology and Operations Practice (STO), Science Leaders & Specialists
Contact name: Sorcha Hayward
Contact email: sorcha.hayward@hrmrecruit.com

Job description

A global, privately owned pharmaceutical group with an extensive portfolio of marketed cancer care products and a robust drug development pipeline are seeking to appoint a number of QC Analysts into their stability and development team in Dublin. The positions will initially be 12 month fixed term contracts.

The Roles

  • QC Development Analyst X 2
  • QC Stability Analyst

As part of the team, you will be reporting into the Analytical Development Manager.

You will be responsible for but not limited to:

  • Analytical testing of raw material and finished product
  • Reviewing of data and documentation to ensure "right first time" is achieved
  • Execution of investigations and trends of finished product results

The Person

QC Development Analyst x 2

  • BSc in Science or related
  • 2 years' GMP Pharmaceutical industry experience
  • 2 years' HPLC experience (essential) OR LC-MS experience (nice to have)
  • Eligible to work and live in Ireland

QC Stability Analyst

  • BSc in Science or related
  • 2 years' GMP Pharmaceutical industry experience
  • Extensive analytical testing experience
  • Experience reviewing and interpreting data and trends
  • Experience troubleshooting and managing investigations

To discover more about this opportunity, apply now or contact Sorcha Hayward at HRM on +353 1 632 18 66 for a confidential discussion.

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Sorcha Hayward

Science Selection Specialist

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