Job Title: Senior Quality Control Analyst
About the Role:
The successful candidate will be responsible for performing quality control testing and analysis of raw materials, as well as maintaining accurate laboratory documentation in compliance with Standard Operating Procedures and Registered Specifications.
Key Responsibilities:
- Perform QC testing (TOC, pH, Conductivity) of water samples.
- Perform analysis of Raw Materials including HPLC, KF, UV, IR and wet chemistry techniques.
- Complete in a timely and accurate manner of laboratory documentation as directed by the QC Material Management Supervisor.
- Compliance with Standard Operating Procedures and Registered Specifications.
- Assist in authoring and reviewing documentation, including SOPs, as required.
- Batch paperwork review, and reconciliation of analysis performed in laboratory.
- Ensure any out of specification results are investigated according to site procedures.
- Support technical transfer of new projects.
- Assist with out of specification investigations and deviations using the Infinity system.
Required Skills and Qualifications:
- A degree in science, engineering or related discipline is essential along with 3 years' experience in a role within the biopharmaceutical/pharmaceutical industry.
- Proven track record of meeting deadlines.
- Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.
Benefits:
This is an exciting opportunity for candidates looking to develop their skills and knowledge in a dynamic and growing industry. The successful candidate will have access to ongoing training and development opportunities.
Others:
Candidates interested in this opportunity should possess a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship.