QC Stability Reviewer
- Posted 17 April 2019
- SalaryNegotiable
- Job type Permanent
- DisciplineLife Sciences & Engineering Technologies, Science Leaders & Specialists
- ReferenceBBBH25398_1555513987
- ContactSorcha Hayward
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.