
Senior Therapeutic Goods Specialist
6 days ago
The role of a GMP Assistant Director in the Manufacturing Quality Branch is a key position that plays a vital part in regulating therapeutic goods in Australia.
This leadership role involves leading a team of staff who evaluate overseas manufacturers to ensure medicinal products supplied to Australia meet internationally recognised quality standards.
Assessments cover Active Pharmaceutical Ingredients, vaccines, prescription and over-the-counter medicines, providing opportunities for growth and expansion in medicines regulation.
The team engages with international regulatory authorities to evaluate equivalency and acceptability of overseas GMP standards within the Australian framework. Domestic and international forums are also attended to support broader goals.
Key Responsibilities
- Leading a team of staff evaluating overseas manufacturers
- Evaluating equivalency and acceptability of overseas GMP standards
- Attending domestic and international forums to support broader goals
Desirable Qualifications
A tertiary qualification in chemistry, biochemistry, microbiology, biotechnology, pharmacy or engineering from an Australian institute or equivalent overseas qualification is highly desirable.
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