Job Description

JOB DETAILS


1 QA batch release of manufactured ‘specials’.
2 Reviewing and approving new formulations, labels, shelf life extensions, repacks and in-house
preparations.
3 Writing, reviewing and approving Quality documentation, including validation protocols and reports,
change controls and Good Manufacturing Practice (GMP) deviations.
4 Assisting with customer and product queries and complaints.
5 Writing, reviewing and approving Standard Operating Procedures (SOPs).
6 Involvement with technical customer queries and product investigations.
7 Responding to enquiries in a timely manner, giving advice on ‘specials’ quality requirements in order to
maintain the company's reputation for customer service and technical acumen.
8 Dealing with the administration and monitoring of the QMS, including change controls, GMP deviations,
technical agreements, validation reports, quality risk assessments, customer complaints, periodic reviews,
self inspection and external audit reports, and SOPs.
9 Conducting/assisting with internal self inspection audits.
10 Participating in regulatory inspections.
11 Ensuring that the business complies with current and future worldwide GMP standards and requirements.
FUNCTIONAL AREA
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