QC Analyst
(6 month contract)
About the Company:
Our client is a Swiss pharmaceutical based corporation that provides solutions to address the evolving needs of patients worldwide. Their main discoveries are development, manufacture and marketing of prescription and generic pharmaceutical products and eye care products.
Primary Responsibilities:
In this role, you will be responsible for all or subset of the key responsibilities below:
- Maintain QC Raw Materials (RM) laboratory in full cGMP compliance.
- Perform raw material method validation/ verification and routine RM release testing such as compendia methods, HPLC, GC, Autotitrator/KF, Identity by FTIR etc.
- Perform data entry, review and approval of RM packages for batch release
- Support laboratory activities such as improvement projects
- Perform technical reviews of procedures and testing monographs for raw materials
- Support/ Lead laboratory investigations (e.g. OOS, deviation)
- Support/ Lead change controls for QC Raw Materials
- Support/ Lead creation and revisions of RM testing monographs
- Prepare and participate in health authority inspections and internal audits
- Other duties or projects assigned by the QC Team Leader-RM
Requirements:
- Diploma or Bachelor’s degree in Science/ Life Science, Pharmaceutical Science or Engineering or any other relevant field
- Minimum 1 years of applied professional work experience in quality control/assurance in pharmaceutical manufacturing environment.
- Experience in QC raw material method validation/ verification and routine RM release testing such as compendia methods, HPLC, GC, Autotitrator/KF, Identity by FTIR etc.
Reg No: R22104540
EA License no: 94C3609
