Micro Labs Hiring 2026 – Quality Control Jobs in Sikkim
Looking for an experienced Quality Control job in the pharmaceutical industry?
Micro Labs Ltd. is inviting applications for Sr. Officer / Sr. Executive – Quality Control positions at its Sikkim manufacturing facility.
The opportunity is aimed at professionals with 3–7 years of relevant experience in pharmaceutical formulation manufacturing and hands-on exposure to analytical instruments, stability studies, method validation and laboratory compliance systems.
Candidates with B.Pharm, M.Pharm or M.Sc qualifications can apply.
Job Overview
| Details | Information |
|---|---|
| Company | Micro Labs Ltd. |
| Department | Quality Control |
| Position | Sr. Officer / Sr. Executive |
| Qualification | B.Pharm / M.Pharm / M.Sc |
| Experience | 3–7 Years |
| Location | Sikkim |
| Industry | Pharmaceutical Formulations |
| Work Type | On-site |
| Application Mode |
About Micro Labs
Micro Labs Ltd. is an established pharmaceutical company with operations across formulation manufacturing and healthcare products.
For experienced QC professionals, working in a formulation environment provides exposure to analytical testing, data integrity, laboratory systems, validation and regulatory compliance.
The current opening is particularly relevant to candidates who already have experience in regulated pharmaceutical manufacturing facilities.
Position – Sr. Officer / Sr. Executive, Quality Control
Department
Quality Control
Qualification
- B.Pharm
- M.Pharm
- M.Sc
Experience
3–7 years of relevant Quality Control experience
Preferred Background
Candidates should have prior experience in pharmaceutical formulation manufacturing.
Analytical Instrument Experience
Applicants should have hands-on experience operating and troubleshooting instruments such as:
- HPLC
- GC
- UPLC
- UV Spectrophotometer
- IR Spectrophotometer
Experience with these systems is important because the position involves analytical testing and laboratory operations.
Key Technical Skills Required
Candidates should have knowledge of:
- Stability testing
- Analytical method validation
- Instrument calibration
- Instrument qualification
- Data integrity
- GLP
- GMP
- GDP
- Laboratory documentation
- Pharmacopoeial requirements
Professionals should also be comfortable working in a compliance-driven QC environment.
Regulatory & Compliance Knowledge
The role may require familiarity with regulatory and quality expectations such as:
- USFDA
- MHRA
- WHO-GMP
- EU-GMP
- ICH Guidelines
- Schedule L1
- Schedule M
- Good Laboratory Practices
- Data Integrity principles
Previous exposure to regulatory audits or inspections can be valuable.
Key Responsibilities
The selected candidate may be responsible for:
- Performing routine and advanced QC analysis
- Operating HPLC, GC, UPLC, UV and IR instruments
- Troubleshooting analytical equipment
- Conducting stability testing
- Supporting analytical method validation
- Performing calibration and qualification of instruments
- Maintaining laboratory records
- Ensuring data integrity
- Following GLP and GMP requirements
- Supporting regulatory audit readiness
- Reviewing analytical data
- Ensuring compliance with approved SOPs and pharmacopoeial requirements
Who Should Apply?
This opportunity is suited to:
- Experienced pharmaceutical QC professionals
- Candidates with formulation manufacturing exposure
- Professionals with strong analytical instrument experience
- Candidates familiar with regulated laboratory environments
- Professionals seeking senior-level QC responsibilities
Freshers are not eligible for this particular opening.
Why Consider This Opportunity?
The role provides professionals with practical exposure to:
- Advanced analytical instruments
- Pharmaceutical formulation QC
- Stability studies
- Method validation
- Regulatory compliance
- Data integrity
- Laboratory investigations
- Global quality standards
This experience can support future progression toward roles such as QC Executive, Senior Executive, Assistant Manager or QC Manager.
How to Apply
Interested candidates can send their updated CV to:
Email: santu.pal@microlabs.in
Contact: +91 6294339843
Immediate joiners may be given preference.
When applying, clearly mention the position:
“Sr. Officer / Sr. Executive – Quality Control”
Important Notes
- Experience requirement: 3–7 years
- Formulation manufacturing experience is expected
- Freshers are not eligible
- Immediate joiners may receive preference
- Candidates should highlight analytical instrument exposure clearly in their CV
Frequently Asked Questions
1. Which position is Micro Labs hiring for?
Micro Labs is hiring for Sr. Officer / Sr. Executive – Quality Control roles.
2. What qualification is required?
Candidates should have B.Pharm, M.Pharm or M.Sc qualifications.
3. How much experience is required?
The role requires 3–7 years of relevant Quality Control experience.
4. Are freshers eligible?
No. This opening is intended for experienced QC professionals.
5. Is formulation experience mandatory?
The supplied recruitment information specifically emphasizes experience in a pharmaceutical formulation manufacturing facility.
6. Which analytical instruments should candidates know?
Hands-on experience with HPLC, GC, UPLC, UV and IR is relevant.
7. What compliance knowledge is useful?
Knowledge of GMP, GDP, GLP, Data Integrity, ICH, Schedule L1 and Schedule M is useful.
