We at MicroCrispr Pvt. Ltd are looking for agile personnel to join the vibrant QA team for cell and gene therapy (CGT) and other Advanced Therapeutic Medicinal Products (ATMPs). If you are a potential fit, kindly share your resume at [email protected] & [email protected]

Opening for QA Verticals:-

- IPQA (In-Process Quality Assurance)
- AQA (Analytical Quality Assurance)
- QMS (Quality Management System)
- Engineering QA/Qualification
- DMS / Documentation QA
- DQA (Development Quality Assurance)
- Data Integrity (DI Officer)
- Computer System Validation (CSV QA)
- Clinical QA
- GLP QA
- Pharmacovigilance QA
- Training QA
- Audit & Compliance QA

Key Responsibilities

- Ensure compliance with cGMP, GDP, GLP, GCP and regulatory guidelines.
- Support Quality Management System (QMS) activities including deviations, CAPA, change control and investigations.
- Perform review and approval of quality documents and records.
- Conduct shop floor monitoring and compliance checks where applicable.




- Maintain data integrity and proper documentation practices.
- Support internal audits, regulatory inspections and compliance activities.
- Coordinate with cross-functional teams such as Production, QC, Engineering and R&D;.
- Ensure timely closure of quality observations and corrective actions.

Qualifications

- B.Tech Biotechnology/M.Tech Biotechnology/M.Sc in Life Sciences/M.Pharma etc.

Experience

- 1 – 10 Years of experience in CGT (Exp will be prefered) Pharma / Biotech / Biopharma industry.

Key Skills

- cGMP / GDP / GLP / GCP knowledge
- Quality Management System (QMS)
- Documentation & Data Integrity
- Audit & Compliance
- Regulatory understanding

Location- Vapi, Gujarat

? Interested candidates may share their updated CV at: [email protected] & [email protected]

📌 Quality Assurance Specialist (Vapi)
🏢 Micro Crispr
📍 Vapi