
Quality Assurance Executive
3 weeks ago
We are recruiting for a greenfield project in GIDC Vapi having area 10,556 sq m for manufacturing Pharma Intermediates and APIs. Planned facilities include main intermediate production building, GMP facility and set-up for Catalytic Hydrogenation, with a strong focus on green chemistry and competitive innovation.
Roles and Responsibilities:
- The candidate will be responsible for preparing and maintaining Engineering/Project documentation, Qualification & Validation documents for greenfield project stage till commercial manufacturing, while ensuring implementation and compliance in line with industry / cGMP best practices.
- Preparation of Qualification document like URS, DQ, IQ, OQ & PQ for production and utility equipments.
- Responsible for Engineering documents of the complete project including certificates, calibration, test results, inspection requests, non-compliance reports and site instruction/observations, permanent materials delivered and other important QA/QC documents.
- Factory acceptance test at vendor site.
- Qualification of new equipment and periodic re-qualifications of equipment i.e. PW plant HVAC etc, facility, utilities.
- Preparation & Review of SOPs for Engineering department.
- Training and Approval of Qualification SOP.
- Preparation of Facility qualification document.
- Preparation and Approval of Project specific qualification plan for all major changes.
- Document Preparation, Installation and operational qualification protocol and reports. Performance Qualification Protocol and reports.
- Responsible for conducting training to new joinees and Executives regarding Qualification Activities.
Qualifications:
- BE / BTech in Chemical / Mechanical Engineering
- 2-4 years in Engineering/Project (Documentation )
- Good written and verbal communication skills
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