Join Micro Labs Limited – Shape Your Future in Pharmaceuticals!
Summary: Micro Labs Limited, a leading pharmaceutical company committed to quality and innovation, is seeking talented and dedicated individuals to join our Verna, Goa facility. We offer diverse opportunities across Production, Quality Assurance, Quality Control, Packing, Engineering, EHS, and TT QC Validation departments. If you’re a motivated B.Pharm, M.Pharm, B.Sc, M.Sc, BE, or Diploma holder looking for a challenging and rewarding career, we encourage you to apply!
About Micro Labs Limited:
Micro Labs Limited is a renowned pharmaceutical manufacturer with a strong presence in the Indian and global markets. We are committed to providing high-quality, affordable medicines and fostering a culture of innovation and excellence. At Micro Labs, we believe in investing in our employees and providing them with opportunities for growth and development.
Open Positions at Our Verna, Goa Facility:
We are currently hiring for the following positions:
1. Packing Department
- Qualification: B.Pharm / M.Pharm
- Experience: 0-5 years
- Responsibilities: Performing and overseeing Blister Packing operations. Ensuring compliance with cGMP guidelines during packing processes. Maintaining accurate records and documentation. Troubleshooting packing equipment issues.
2. Production Department
- Qualification: B.Pharm / M.Pharm
- Experience: 0-5 years
- Sections: Compression / Granulation
- Responsibilities: Operating and maintaining compression or granulation equipment. Adhering to SOPs and batch manufacturing records. Monitoring production parameters and ensuring product quality. Participating in equipment cleaning and sanitization activities.
3. Quality Assurance (QA)
- Qualification: B.Pharm / M.Pharm
- Experience: 2-10 years
- Areas: Process Validation, Investigation Team, Market Complaints, Vendor Qualification, Artwork
- Responsibilities:
- Process Validation: Developing and executing validation protocols, analyzing validation data, and preparing validation reports.
- Investigation Team: Participating in investigations of deviations, OOS results, and customer complaints.
- Market Complaints: Handling and resolving market complaints related to product quality.
- Vendor Qualification: Auditing and qualifying vendors of raw materials and packaging materials.
- Artwork: Reviewing and approving artwork for packaging materials. Ensuring compliance with regulatory requirements.
4. Quality Control (QC)
- Qualification: B.Sc / M.Sc
- Experience: 2-8 years
- Responsibilities:
- Analyzing Raw Materials (RM), Packaging Materials (PM), stability samples, and finished products according to pharmacopoeial and in-house methods.
- Performing analytical testing using HPLC, GC, UV-Vis spectrophotometer, and other instruments.
- Maintaining accurate records of analysis and reporting results.
- Troubleshooting analytical issues and participating in method development and validation activities.
5. TT QC Validation (Method Validation & Transfer)
- Qualification: B.Sc / M.Sc
- Experience: 3-8 years
- Responsibilities:
- Performing method validation activities for analytical methods.
- Executing method transfer protocols from R&D to QC or between different QC labs.
- Preparing validation and transfer reports.
- Ensuring compliance with regulatory guidelines for method validation and transfer.
6. Engineering
- Qualification: BE Electrical/Mechanical / Diploma Draughtsman
- Experience: 0-5 years
- Requirement: Process Engineering
- Responsibilities: Supporting process equipment maintenance and troubleshooting. Assisting in the design and implementation of new equipment and systems. Ensuring compliance with safety regulations and engineering standards. Performing preventive maintenance activities.
7. Environment, Health & Safety (EHS)
- Qualification: B.Sc / BE Electrical/Mechanical / Diploma
- Experience: 0-5 years
- Requirement: ADIS certification + Pharma EHS experience
- Responsibilities: Implementing and maintaining EHS programs. Conducting safety audits and inspections. Providing EHS training to employees. Investigating accidents and incidents. Ensuring compliance with environmental regulations.
Key Responsibilities (General):
- Ensure strict compliance with cGMP (Current Good Manufacturing Practices) and other relevant regulatory guidelines.
- Perform assigned tasks related to production, packing, quality assurance, or quality control with precision and efficiency.
- Conduct analytical testing using sophisticated instruments like HPLC and maintain accurate records.
- Actively participate in validation activities, investigations, and comprehensive documentation processes.
- Contribute to the upkeep of equipment, utilities, and uphold stringent safety standards.
Required Qualifications:
- A degree in Pharmacy (B.Pharm, M.Pharm), Science (B.Sc, M.Sc), or Engineering (BE), depending on the specific department requirements.
- Relevant hands-on experience in the pharmaceutical industry (freshers are encouraged to apply for select positions).
- A thorough understanding of GMP, GDP (Good Documentation Practices), and pharma manufacturing processes.
- Proficiency in the operation and maintenance of analytical instruments (for QC roles).
- ADIS certification is mandatory for EHS positions.
Benefits of Joining Micro Labs Limited:
- Competitive salary commensurate with experience and qualifications (ranging from ₹2.2 LPA to ₹9.5 LPA).
- Exceptional career growth opportunities within a leading Indian pharmaceutical company.
- Exposure to cutting-edge, technology-driven manufacturing systems and processes.
- A stable and supportive work environment with a strong emphasis on continuous learning and development.
- Comprehensive benefits package.
How to Apply:
If you meet the above qualifications and are eager to contribute to a dynamic and growing organization, we encourage you to apply! Please send your updated CV to:
- Email: [email protected]
- Location: Verna Industrial Estate, Goa
We look forward to receiving your application and exploring how your skills and experience can contribute to the success of Micro Labs Limited.