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.