Requirements:
- Grade 12
- Degree / National Diploma in Analytical Chemistry and / or BSc majoring in Chemistry
- Minimum 3 to 5 years' working experience in a Pharmaceutical Lab
- Experience in evaluation and compilation of methods of analysis
- Experience in international GMP / GLP requirements
- Experience in Quality Management Systems
- HPLC, GC, AA, UV-Vis and FTIR experience

Responsibilities:
- Evaluate data packs for all new raw materials, bulk, finished products, components and consumables
- Evaluate change control requests for specifications updates
- Verify and log changes requested
- Advise on any further evaluation / validation required for compilation of specifications / methods
- Liaise with Buyer regarding purchase of new reagents, standards, columns and consumables needed
- Identify and issue new item numbers
- Analyse samples to support compilation of new analytical methods
- Compile reports of analytical data generated
- Accurately interpret and calculate results
- Perform quality review of analytical data according to set schedule
- Ensure that all OOS investigations are executed and completed as required
- Report all OOS's to management
- Assist in OOS data trends
- Ensure that all records are evaluated and correct before sending to the quality department
- Investigate and initiate corrective actions for all quality deficiencies
- Ensure compliance with GLP / GMP requirements
- Ensure that all products are produced, tested and stored according to SOP's