Validation Technician

5 months ago


Epping, South Africa Aspen Pharma Group Full time

**JOB REQUIREMENTS**:

- Matric/Grade 12 with Mathematics and Science
- Technical / Engineering qualification which has been completed or studying towards the completion of your qualification (part-time)
- At least 1-3 years’ experience in a cGMP environment preferably in the pharma industry
- Technical experience would be an advantage, in chemical and mechanical processing equipment /systems

**BASIC JOB FUNCTIONS**:

- To provide technical and administrative support for the validation section responsible for equipment qualification
- Report to the senior validation team
- Drafting, executing, and reporting on equipment qualifications for new and existing equipment, systems, and utilities used in the manufacturing of intermediate and finished active pharmaceutical ingredients (API)
- Maintain administration required for qualification documentation as per relevant SOPs
- Liaise with various departments, suppliers, and external contractors regarding validation qualifications
- Witness/execute qualification trials/tests/activities (IQ/OQ/FAT/SAT etc.)
- Preparation of validation qualification documentation for audits, internal and external
- Assist with closure of equipment change controls related to projects worked on
- Maintain engineering/validation databases.
- Comply with GMP requirements as outlined by Company SOP's and written instructions in all tasks and activities.

**PERSONAL ATTRIBUTES (Brief Summary)**:

- Excellent verbal & written communication skills
- Must have the ability to work within a challenging environment
- Must be numerate and show attention to accuracy
- Good organisational skills, hands-on and pro-active
- Good intrapersonal and interpersonal skills
- Proficient in Microsoft Office
- Ability to work at heights and confined spaces
- Proficient report writing skills



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