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QA Specialist
About the job
Job Title: Quality Assurance (QA) Specialist
About the Job
We are seeking a Quality Assurance Specialist with solid experience in Quality Management Systems (QMS) and the capability to draft, review, and implement Standard Operating Procedures (SOPs). The ideal candidate will join PPI’s Quality team and support manufacturing and inventory activities while ensuring full compliance with GMP standards.
Key Responsibilities
- Ensure all manufacturing activities comply with GMP requirements and prevent any potential cross contamination.
- Verify adherence to all procedures related to production operations.
- Inspect and sample received bulk products.
- Inspect machines and production lines for cleanliness.
- Manage and review batch records.
- Perform in process checks and daily production floor rounds.
- Collect medicinal product samples.
- Conduct material and product reconciliation.
- Manage and store pharmaceutical waste.
- Review generated operational records.
- Control weighed and dispensed materials.
- Collect reference and retention samples.
- Handle quarantine and rejected materials, destruction processes, and returned goods.
- Support quality investigations and deviation assessments.
Qualifications & Skills
- Bachelor’s degree in Science, Pharmacy, or a related field.
- Minimum of 2 years of experience in Quality Assurance within the pharmaceutical industry.
- Strong knowledge of cGMP requirements.
- Good English communication skills (reading, writing, speaking).
- Good computer skills.
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To apply, please click here for available vacancies.