Chemical Analyst (Gqeberha)
Aspen Pharma Group · Port Elizabeth, Eastern Cape
Stop applying one at a time.
JobAlertsZA auto-applies to South African jobs like this one for you, overnight. Upload your CV once — we do the applying.
Start free — we apply for you →Description
- Conducts chemical and quality testing on raw materials, in-process samples and finished products to ensure products meet GMP, quality and specification requirements. Provides accurate test results and supports Production and Quality Control.
Requirements
- Perform chemical and quality testing on raw materials, in-process samples and finished products.
- Prepare and analyse samples according to approved SOPs and testing methods.
- Perform HPLC, GC and other required laboratory analyses.
- Conduct stability testing and routine quality testing as required.
- Ensure all testing is completed accurately and within required timelines.
- Operate laboratory equipment correctly and ensure equipment is maintained and calibrated.
- Record, review and report test results accurately and ensure all laboratory documentation is complete.
- Ensure all testing activities comply with GMP, SOPs, safety requirements and quality standards.
- Identify, investigate and escalate abnormal results, testing errors and deviations.
- Provide accurate laboratory results and technical feedback to Production, QA and other relevant departments.
- Support investigations into out-of-specification and other laboratory-related issues.
- Maintain good laboratory housekeeping and ensure samples, records and equipment are properly managed.
- Assist with improving laboratory methods, processes and testing efficiency.
- Ensure laboratory records and reports are maintained in accordance with regulatory requirements.
- Monitor testing progress and communicate any delays or issues to the QC Team Leader.
- Support internal and external audits by ensuring laboratory records and processes are accurate and compliant.
- Maintain knowledge of relevant analytical methods, pharmaceutical testing requirements and quality standards.
Qualification
- National Diploma in Analytical Chemistry or a related Chemistry/Laboratory qualification.
Experience
- Minimum 2 years' relevant laboratory/analytical chemistry experience, preferably in a pharmaceutical or regulated manufacturing environment. Experience with HPLC and GC is required/preferred.