Micro Labs Ltd., a leading pharmaceutical company, is hiring experienced professionals for its Quality Control (QC) Department at its Sikkim manufacturing facility. The opening is specifically for candidates with 3–7 years of pharmaceutical QC experience and strong analytical laboratory exposure.

Job Details

Key Responsibilities

Candidates should have hands-on experience in:

• Operation and troubleshooting of HPLC, GC, UPLC, UV and IR spectrophotometers
• Stability testing
• Analytical method validation
• Calibration and qualification of QC instruments and equipment
• GMP, GDP and GLP requirements
• Data Integrity requirements
• Pharmacopoeial requirements
• ICH Guidelines
• Schedule L1 & M requirements
• Analytical laboratory operations
• Regulatory compliance

Preferred Candidate Profile

The company specifically prefers candidates with:

• Pharmaceutical manufacturing experience
• Experience in a formulation manufacturing company — mentioned as mandatory in the advertisement
• Strong analytical skills
• Strong documentation and compliance skills
• Exposure to regulatory standards and inspections such as:
  • USFDA
  • MHRA
  • WHO-GMP
  • EU-GMP
• Immediate joiners will be preferred.

Important: This opportunity is specifically for experienced Quality Control professionals. Freshers and candidates from other functions are requested not to apply.

Ideal Candidate

M.Pharm / B.Pharm / M.Sc + 3–7 years Pharma QC experience + HPLC/GC/UPLC + stability testing + method validation + regulatory compliance

Candidates with experience in formulation manufacturing QC and exposure to regulated markets will be particularly relevant.

Apply Now

📧 Email: santu.pal@microlabs.in
📞 Contact: +91 6294339843

Interested candidates meeting the above requirements can apply with their updated CV.