IPCA Laboratories Ltd., one of India’s leading pharmaceutical companies, has announced an exciting recruitment drive for experienced professionals at its Sikkim manufacturing facility. The company is inviting applications for multiple Officer-level positions across Quality Control, Engineering, Production, Quality Assurance, and Store departments.
If you have relevant pharmaceutical manufacturing experience and are looking to build your career with a reputed organization, this is an excellent opportunity.
Company Overview
Company Name: IPCA Laboratories Ltd.
Industry: Pharmaceutical Manufacturing
Job Location: Sikkim
Job Type: Full-Time
Experience Required: 2–10 Years (Department-wise)
Mode of Application: Email
Current Job Openings
1. QC – HPLC
Designation:
Junior Officer
Officer
Experience Required: 3–5 Years
Key Responsibilities:
Analysis of Raw Materials (RM) and Finished Goods (FG) using HPLC
Method validation
Documentation
Instrument handling
Compliance with GMP, GLP, and Data Integrity requirements
2. Engineering – Electrical & Mechanical
Designation:
Officer
Experience Required: 3–5 Years
Key Responsibilities:
Electrical and mechanical maintenance
Machine troubleshooting
Preventive maintenance
Utilities and equipment management
3. Production – Compression
Designation:
Officer
Experience Required: 2–6 Years
Key Responsibilities:
Compression machine operation
Machine handling
KPI monitoring
Documentation
GMP compliance
4. Lab QA
Designation:
Officer
Experience Required: 3–5 Years
Key Responsibilities:
Documentation review
Change control and deviation handling
CAPA
OOS/OOT investigations
GMP compliance
5. QA Executive (QMS & IPQA)
Designation:
Executive
Experience Required: 8–10 Years
Key Responsibilities:
QMS & IPQA activities
Process and site audits
Supplier audits
Continuous improvement initiatives
Compliance monitoring
6. Store Office
Designation:
Officer
Experience Required: 2–6 Years
Key Responsibilities:
Material receipt and issuance
Stock management
Documentation and record keeping
Coordination with Accounts
Inventory and vendor management
Why Join IPCA Laboratories?
Excellent career growth opportunities
Learning and professional development
Work with an experienced pharmaceutical team
Safe and inclusive workplace
Opportunity to contribute to quality healthcare
Eligibility Criteria
Candidates should possess relevant educational qualifications and pharmaceutical industry experience matching the applied department. Strong knowledge of GMP documentation, SOP compliance, and department-specific technical skills will be preferred.
Application Process
Interested candidates should send their updated CV via email.
Email IDs:
sangita.sharma@ipca.com
amardeep.negi@ipca.com
Subject Line Format: Position Applied For – Your Name
Job Location
Sikkim, India
Important Notes
Apply only if your experience matches the required department.
Ensure your resume is updated with current experience and technical skills.
Mention the correct position in the email subject line.
Shortlisted candidates will be contacted by the recruitment team.
Technical FAQs
1. What is HPLC and why is it important in pharmaceutical QC?
HPLC (High-Performance Liquid Chromatography) is an analytical technique used to identify and quantify pharmaceutical compounds. It ensures products meet quality specifications before release.
2. What is the difference between GMP and GLP?
GMP (Good Manufacturing Practices) focuses on manufacturing quality, while GLP (Good Laboratory Practices) ensures laboratory testing is performed consistently, accurately, and with proper documentation.
3. What do CAPA, OOS, and OOT mean in Quality Assurance?
CAPA: Corrective and Preventive Action
OOS: Out of Specification
OOT: Out of Trend
These systems help investigate quality issues and prevent recurrence.
4. What is IPQA in pharmaceutical manufacturing?
IPQA (In-Process Quality Assurance) monitors manufacturing activities in real time to ensure compliance with GMP, SOPs, and approved processes throughout production.
5. What skills are expected for Production Compression and Engineering roles?
Candidates should have hands-on experience in machine operation, preventive maintenance, troubleshooting, equipment handling, documentation, KPI monitoring, and compliance with GMP and safety standards.

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