We are a technology-focused, multi-dimensional pharmaceutical company having state-of-the-art manufacturing capabilities in diverse therapeutic areas such as Cardiology, Diabetology, Pain Management, Dermatology, Ophthalmology, Neurology and more. We strive towards unlocking the power of science to provide access to affordable and innovative medicines to improve health outcomes and make a difference in people’s lives across the globe.
As we continue to champion the cause of Make-in-India through our steady expansion across various Indian states, we create job opportunities and drive social responsibility programs in education, healthcare, rural development and environmental protection to add value to our local communities. Our roadmap is to continue investing in discovering, developing, manufacturing, and commercializing innovative medicines. Meeting the growth and profitability goals through successful innovation in digital healthcare trends and commercial excellence will continue to be the driving factors over the next decade.
Apply:
- Interested candidates can share your resume to goahr@microlabs.in and vinitagavander@microlabs.in
1. Method Validation
Key Responsibilities:
- Perform validation and qualification of analytical methods.
- Prepare validation protocols, reports, and documentation.
Requirements:
- Minimum of 2 years and up 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.
We have exciting career opportunities at Micro Labs Ltd (Goa Plant )
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