Entrepreneurship in the territories: is it the right time?
Human Nature (Gandang Kalikasan, Inc.), is currently the leading brand of natural cosmetics and personal/home care products in the country today. More than being known for our world-class products, we are primarily a social enterprise driven by the core philosophy of Pro-Philippines, Pro-Poor, and Pro-Environment seeking to inspire more businesses to better serve society. Our products showcase the quality and ingenuity of 100% Philippine-made products and our company operates to bring quality life to the poor.
We are looking for a QA Process Specialist is responsible in ensuring GMP, GDP and data integrity are strictly followed in the production area and QA.
Your responsibilities include :
- Analytical testing pH, SG and Viscosity. Signing of all analytical records as the Chemist in-charge.
- In-line monitoring of filling lines and GMP compliance of the are
- Compliance on Good Documentation Practice and data integrity
Detailed job description :
- Verify cleaning and sanitization of equipment, utensils (including pails/orocan and contains), areas and/or rooms that will be used by operations.
- Conduct analytical testing for bulk samples after compounding and filling (Physico Chemico testing: pH, viscosity, specific gravity, appearance, color, odor etc.).
- Keep push-button and bulk samples for micro testing.
- Responsible for ensuring compliance to Good Manufacturing Practice in the production area.
- Ensure compliance to line clearance prior to production and filling operations.
- Verify that the temperature and relative humidity (RH) are within specification in all areas of production.
- Review raw materials dispensing for accuracy of weights of RM and the corresponding RM ticket issued by dispenser.
- Work with production in ensuring that FGs will meet the micro requirements. The concurrent will also be responsible to ensure compliance to WIP monitoring and completion, productivity targets, monitoring usage of alcohol and other production supplies.
- Verify compliance to GKI quality requirements on C & S, filling (including coding) and GMP during production. Ensure timely feedback and escalation for any observed non-compliances.
- Creates Non-Conformity Report (NCR) and ensure that CAPA (Corrective and Preventive Action Plans) are implemented to avoid recurrence.
- Participates in cross-functional investigation and use promote use of quality control tools to investigate and identify the Root Cause and Corrective/Preventive Action plans.
- Comply with Good Documentation Practices (GDP).
- Participates in GMP (Internal Company Audit) and provide required documents for compliance.
- Stop the production or call-out to QA Head/Chairman of GKI for any non-compliance observes during the production of products.
