– Must be a Registered Pharmacist or Chemical Engineer, with available license.
– With at least 5 years of supervisory experience in pharmaceutical manufacturing industry
– Has a wide knowledge and experience in production planning, pharmaceutical equipment, root cause analysis and
– Has experience in Quality Assurance, Quality Risk Management, GMP Certification , ISO Certification, and Pharmaceutical Validation
– Must have hands on experience in production operations or quality assurance esp. for solid dose forms.
– Strong leadership, analytical and judgmental skills.
– Must be a person of integrity and honesty.
– Must know how to value teamwork
– Must possess time-management and stress-management skills.
– Must be willing to work in Silang, Cavite
* Ensures that all processes adhere to Quality Assurance and Quality Control standards in the pharmaceutical industry
* Enforces Quality System and proper product production, to produce quality products.