Job Description
conduct analytical testing on commercial, stability and non-routine samples, in an FDA regulated environment with a healthcare company based in Galway.
The successful candidate will participate in the test method development, validation and technical transfers as required.
This role is a fixed term contract, with view to longer-term or permanency.
Responsibilities of Analytical Chemist:
Conduct raw material, in process, finished product and Stability testing. Test method development and validation may also be required.
Complete documentation associated with testing/ method development & Validation/ equipment qualification in a timely manner.
Ensure all analytical testing is carried out as defined in the Quality System
Perform equipment calibration and qualification as required.
Provide analytical support to process validations.
Participate in Regulatory, Internal and Vendor audit programs as required.
Provide training, technical guidance / trouble shooting to junior laboratory staff.
Review of Laboratory results and documentation.
Perform and assist with additional duties as may be directed by the QC supervisor.
Requirements of Analytical Chemist:
Bachelor's Degree in Analytical Chemistry, Science or similar discipline.
3+ years work experience as a Chemist within a GMP Quality Control environment in the Pharmaceutical Industry.
Proven working experience of; HPLC, GC, UV and Near IR.
Strong experience of Quality Systems required to support GMP Analytical Laboratory.
Please contact Larry on 01-2302400 / larry@rftgroup.ie / www.rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.
Key Words; FDA, GMP, Chemistry, Analytical, R&D, Research and Development, Analytical Chemistry, Troubleshooting, Test Methods, Method Transfer, Quality Control, Pharmaceutical, Medical Device, HPLC, GC, Karl-Fischer, Ireland, Galway, Clare.