Senior Executive, Chemical Process

Key Responsibilities:

1. Prepare, review and maintain GMP documentation include but not limit to batch records, protocols, reports, risk assessment, impact assessment, Standard Operating Procedures and Equipment Operating Procedures
2. Ensure accuracy, completeness, and compliance of all documentation with applicable GMP requirements
3. Prepare e investigation reports and implement appropriate corrective and preventive actions (CAPA)
4. Support facility expansion projects and equipment installation activities
5. Review qualification protocols and reports to ensure compliance with GMP requirements
6. Ensure compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company quality standards
7. Follow Environmental Health and Safety (EHS) policies and procedures at all times
8. Support internal and external audits, inspections, and compliance initiatives.
9. Update and maintain Batch Manufacturing Records and other GMP documentation in accordance with ALCOA++ principles.
10. Adherence to Standard Operating Procedures, Operational Control Procedures

Qualifications:

1. Bachelor's degree in chemical engineering / manufacturing engineering / Biotech Engineering
2. Years of Experience: 4 years to 6 years
3. Preferred Industry: Industry with GMP background (added advantage)