Micro Labs Ltd is seeking talented professionals for various positions at our Goa Plant. Join our team and contribute to our mission of delivering excellence in pharmaceutical manufacturing and quality assurance.
Open Positions
1. Method Validation
Key Responsibilities:
- Perform validation and qualification of analytical methods.
- Prepare validation protocols, reports, and documentation.
Requirements:
- 2 to 5 years of experience in Method Validation.
- Strong knowledge of analytical techniques and industry standards.
- Excellent attention to detail and documentation skills.
2. Quality Assurance in 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:
- 4 to 10 years of experience in Validation.
- In-depth knowledge of GMP, GxP, and related regulations.
- Strong 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:
- 4 to 8 years of experience in Audit and Compliance.
- Thorough understanding of regulatory requirements (FDA, EMA, etc.).
- Experience in conducting audits and preparing audit reports.
How to Apply
Interested candidates can share their resumes at:
📧 Email: goahr@microlabs.in and vinitagavander@microlabs.in
Join Micro Labs Ltd and take the next step in your career with us! 🚀