My client a world leader in healthcare urgently require a Quality Officer
He/she will manage and co-ordinate Quality Assurance activities and resources associated with the Pharmaceutical manufacturing and release of Products.
In the role one will be responsible for compliance in-house requirements and cGMPs.
Whay you'll need :
- Responsible for the continuous review of the CAPA & Internal & Compliance programs.
- Can implement process improvements to ensure predictable processes across all lines.
- Responsible for facility compliance with regulatory commitments, in-house requirements & GMP.
- Introduction of quality systems in line with industry practices and GMP requirements.
- Preparation of procedures and policies for area of responsibility
- Responsibility for maintenance and development of GMP awareness facility-wide, including:
- Preparation and execution of training programmes, assessment of GMP training requirements etc.
- Investigation for QA review of all GMP critical documents.
- In-house auditing.
- Line clearance procedures.
- Exception and deviation management e.g. deviations, Alarms, OOS, etc.
- Validation: Define process, product and test method validation requirements,
- Compilation of required Regulatory documentation.
- Educational Requirements:
- Minimum qualification: BSC/BEng degree.
- Familiar with Quality Systems: ISO 17025, ISO 14001, OHSAS 18001
- Minimum of 3 years experience in a QA role within a regulated environment.
- For more information please call Colin by E-Mail firstname.lastname@example.org
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