QA Inspector

2 weeks ago


Epping, South Africa Aspen Pharma Group Full time

**BASIC JOB FUNCTIONS (Brief Summary)**:

- Carrying out site audits
- Document/report writing, reviewing, issuing, and change control
- Preparing the site for external audits and Regulatory Inspections
- Verification of validation activities within the nominated manufacturing area
- Producing and checking labels for raw materials, intermediates, and finished goods according to the set standard operating procedures and master schedule of standard labels
- Checking the issuing of tamper-evident packaging components according to the set procedure
- Ensuring production is in compliance with cGMP, the BPR instructions, and all related SOPs
- Reviewing BPRs and raising deviations where necessary
- Assisting with the batch release procedure
- Maintaining the electronic databases related to the batches released
- Maintaining relevant filing systems that ensure traceability of the position’s functions
- Investigating and documenting deviations
- Understanding and complying with all relevant SOPs
- Facilitate training in compliance with cGMP
- Performing internal audits

**PERSONAL ATTRIBUTES (Brief Summary)**:

- Observation - ability to observe and evaluate processes and procedures
- Excellent organisational and administrative skills
- Excellent problem-solving skills
- Attention to detail - proofreading and auditing
- Ability to communicate with all levels of the business
- Ability to interpret regulations and take initiative
- Confident to address adverse issues at all levels of the business

**JOB REQUIREMENTS**:

- Minimum Matric / Grade 12 with Mathematics & Science
- A tertiary qualification - National Diploma/BTech in Quality or BSc Chemistry or Life Sciences or Equivalent Qualification as per the National Qualifications Framework (NQF) - SAQA would be considered
- Must be computer literate, MS Windows, i.e., Word, Excel, PowerPoint, etc.
- Validation and Production experience will be advantageous