Job Description
SUMMARY OF RESPONSIBILITIES
- Manages and maintains a database for the quality system and prepares/assists in the preparation of monthly and annual reports and quality trending reports
- Reports the status of the quality levels of staff, systems and production activities and participates in improvement program
- Participates in the evaluation of quality events, incidents and possible complaints and the follow-up activities.
- Keep up to date with all related quality legislation and compliance issues
- Coordination of Staff GMP Training
- Handling of obsolete/rejected raw and packaging materials
- Management of deviations and non-conformities in production processes and follow up on CAPA
- Manage internal and external audit programmes which includes preparing CAPA plans and close out of compliance directives
- Writing, reviewing, distributing and filing of completed Quality Management System documents.
- Handling of Product Complaint and reporting on investigations carried out and submission of investigation report
Qualifications
- Bachelor’s Degree in Industrial Chemistry
- A Master’s Degree in Environmental Management.
- 10 years of relevant pharmaceutical manufacturing experience.
A Few Required Competencies:
- Team work.
- Problem Solving.
- Good communication.
- Good decision making.
What we Offer:
- Competitive salary and performance bonus.
- A dynamic work environment that fosters career development and growth opportunities.
- Medical insurance and retirement benefits, etc.