Responsibilities:- Ensures that the GMP Manual and Quality Manual are carefully read and understood, and uses this document as reference when performing quality-related works.
Ensure that all operations and documentations are carries out as per SOP and as per PIC/S GMP requirements.- Strictly observes the Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Safety Standards in the performance of duty at all times.
Participates in the validation and audit activities of the company when needed.
- Observes safety rules and regulations, and keeps work area clean and orderly (Clean as you go)
Candidate must possess a Bachelor's/College Degree in Chemical Engineering, Pharmacy/Pharmacology, or equivalent.
- Must have Professional Regulations Commission (PRC) license.
Preferably with at least 1-2 years experience as QA Engineer preferably in pharmaceutical of manufacturing set-up.- Knowledgeable on Statistical Process Control (SPC), moderate to advance expertise in Microsoft Excel or similar tools, Familiar with 7 QC Tools, Pharmaceutical Manufacturing Knowledge, project management
Team player, cooperative, with initiative to learn and help, responsible, can work with minimum supervision and willing to give inputs or share ideas.
- Can start as soon as possible
Job Types: Full-time, Permanent
Pay: Php18,
- 00 - Php23,000.00 per month
Benefits: - Company Christmas gift
Company events Life insurance
Schedule:
Monday to Friday
Supplemental pay types: Overtime pay
