Quality Assurance Executive

2 - 4 years

0 Lacs

Posted:1 day ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

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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