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

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

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