Job Summary:
The InProcess Quality Assurance Executive will be responsible for ensuring that all products are manufactured and packaged in accordance with cGMP and other regulatory standards. The position will work closely with production teams to monitor and verify the quality of products throughout the manufacturing process.
Key Responsibilities:
- Ensure quality is maintained from warehouse to production and packing.
- Ensure compliance with cGMP and other regulatory requirements for the manufacturing and packaging of products.
- Work closely with production teams to identify and resolve quality issues in realtime.
- Participate in investigations of deviations and nonconformances and provide support for root cause analysis and corrective and preventive actions (CAPAs).
- Maintain accurate and complete documentation of all qualityrelated activities.
- Participate in internal and external audits and inspections and provide support for the preparation of responses to findings and observations.
- Provide guidance and training to production personnel on qualityrelated topics.
- Participate in the development and review of qualityrelated procedures and policies.
- Stay uptodate with the latest regulatory requirements and industry best practices for inprocess quality assurance.
Qualifications:
- Bachelors degree in Chemistry Biochemistry Pharmacy or related field.
- At least 1 year of experience in inprocess quality assurance in the pharmaceutical industry.
- Strong knowledge of cGMP and other regulatory standards for inprocess quality assurance.
- Excellent problemsolving communication and interpersonal skills.
- Ability to work independently and in a team environment.
- Experience in participating in investigations of deviations and nonconformances and providing support for root cause analysis and CAPAs.
- Strong analytical and documentation skills.
- Experience in participating in internal and external audits and inspections.
Required Experience:
Junior IC