
Pharmaceutical Quality Specialist
6 days ago
This role plays a vital part in ensuring the pharmaceutical compounding centre operates in compliance with regulatory and GMP requirements.
The successful candidate will contribute to ongoing continuous improvement in Quality performance across the site, implementing improvements to raise compliance and efficiency.
Key Responsibilities:
- Release of compounded batches
- Participation in investigation and root cause analysis of non-conformances, supplier and customer complaints
- Participation in risk assessment, change control, validation, internal audits, document reviews, CAPA and recall activities
- Liaising with relevant stakeholders to complete action items related to the above
- Conducting and coordinating training on Quality procedures and requirements
- Supporting the team with Environmental Monitoring activities and performing quality assessments quarantined incoming goods as required
The ideal candidate will have experience in a GMP compliant pharmaceutical manufacturing environment, sterile compounding environment, and continuous quality improvement. They should be competent in common IT software, time and task management, and have a tertiary qualification in a Science discipline.
Required Skills and Qualifications:
- Experience in GMP compliant pharmaceutical manufacturing
- Knowledge of sterile compounding environment
- Continuous quality improvement skills
- Competence in common IT software
- Time and task management skills
- Tertiary qualification in a Science discipline
Benefits:
This is an excellent opportunity to join a dynamic team and make a meaningful contribution to the company's success.
Others:
We are committed to providing a safe and supportive work environment that promotes professional growth and development.
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