Join our team at Micro Labs Ltd (Goa Plant) and be a part of a leading pharmaceutical organization. We are currently hiring for multiple roles across departments.
1. Method Validation
Key Responsibilities:
- Perform validation and qualification of analytical methods
- Prepare validation protocols, reports, and supporting documentation
Requirements:
- Experience: 2–5 years in Method Validation
- Strong knowledge of analytical techniques and industry standards
- Excellent attention to detail and proficiency in documentation
2. Quality Assurance – Process Validation
Key Responsibilities:
- Oversee and manage process validation activities
- Ensure compliance with regulatory requirements and industry standards
- Develop and execute process validation protocols and reports
Requirements:
- Experience: 4–10 years in Validation
- Strong knowledge of GMP, GxP, and related regulations
- Excellent communication and problem-solving skills
3. Audit and Compliance
Key Responsibilities:
- Conduct internal audits to ensure compliance with quality standards and regulations
- Assist in preparing for external audits and regulatory inspections
- Review and analyze compliance-related documentation and processes
Requirements:
- Experience: 4–8 years in Audit and Compliance
- Comprehensive understanding of regulatory requirements (FDA, EMA, etc.)
- Hands-on experience in conducting audits and preparing detailed audit reports
How to Apply
If you’re ready to take the next step in your career, share your resume with us:
Become part of our dynamic team and grow with Micro Labs Ltd!
