5 Days Week with Flexi Work Arrangement Options offered
Responsibilities
Perform all activities in the system life cycle of QC laboratory equipment
Set up and maintain QC Processes and QC support of Continued Process Verification and / or Annual Product Reviews
Document all results in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.
Lead QC Processes / Systems-related investigations and projects for improvement of QC processes
Lead and conduct investigations for deviations affecting QC laboratory systems or processes
Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements and that they are filed in accordance to existing policies.
Develop test methods or instrument Standard Operating Procedures (SOPs), write and update Quality Procedures.
Prepare analytical and microbiological for Annual Product Review Reports (APRR).
Requirements
Degree or Diploma in Science (preferably Chemistry) or Chemical Process Technology
Demonstrated QC experience in the pharmaceutical or related industry
Comprehensive knowledge of analytical laboratory equipment system life cycle and data integrity requirements.
Comprehensive knowledge of cGMPs and QC processes
Fully complete Covid-19 vaccination; successful candidates may need to produce official vaccination certificate
Salary will commensurate according to Candidates\xe2\x80\x99 Work Experience & Qualifications To apply for this job opportunity, click on APPLY NOW. We regret that only short-listed candidates will be contacted shortly. EA License No: 14C7092 EA Registration No: R2199193 (Frieda Chan)
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