Current: English
Ipca Laboratories Limited, one of India’s leading pharmaceutical companies, is inviting applications from qualified and experienced professionals for multiple positions in the Engineering (QMS), Lab QA, and Quality Control (QC) departments at its Gandhidham, Gujarat location.
This is an excellent opportunity for candidates looking to build a successful career in the pharmaceutical industry with a reputed organization known for quality, innovation, and regulatory compliance.
Available Positions
1. Engineering – QMS
Designation: Officer / Senior Officer
Qualification:
B.E. / B.Tech / M.Tech or relevant qualification
Experience:
4–6 Years
Key Responsibilities:
QMS & SOP Preparation
Change Control, CAPA & Deviation Management
IQ, OQ & PQ Documentation
Validation & Qualification Activities
HVAC, Water System, DG & Boiler Management
GMP, GDP, ALCOA++ & Data Integrity Compliance
EDMS, LMS, TrackWise & LIMS Operations
2. Lab QA
Designation: Junior Officer / Officer
Qualification:
B.Sc / M.Sc / B.Pharm / M.Pharm or relevant qualification
Experience:
2–4 Years
Key Responsibilities:
HPLC, GC, UV, IR, DT & Dissolution Review
Instrument Calibration Activities
Audit Trail Review & Data Verification
OOS/OOT Investigation
CAPA & Laboratory Investigation
QMS, GMP, GDP & Data Integrity Compliance
EDMS, LMS, LIMS, Chromeleon & TrackWise Knowledge
3. Quality Control (QC)
Designation: Assistant Technician / Technician
Qualification:
D.Pharm / ITI / B.A / B.Com or relevant qualification
Experience:
0–1 Year
Key Responsibilities:
QC Instrument Handling
Sample Analysis Support
GMP & GDP Compliance
ALCOA++ and Data Integrity Awareness
Pharmaceutical Manufacturing Practices
Job Location
📍 Gandhidham, Gujarat
How to Apply?
Interested candidates can share their updated CV to:
📧 shivendrav.singh@ipca.com
Mention the department name in the email subject line:
Engineering – QMS
Lab QA
QC Technician
Technical FAQs
1. What is CAPA in the pharmaceutical industry?
CAPA (Corrective and Preventive Action) is a systematic approach used to identify root causes of deviations, complaints, or quality issues and implement actions to prevent recurrence.
2. What is the difference between OOS and OOT?
OOS (Out of Specification): Test results outside predefined specifications.
OOT (Out of Trend): Results within specifications but showing unusual trends compared to historical data.
3. What is ALCOA++ in Data Integrity?
ALCOA++ principles ensure data is:
Attributable
Legible
Contemporaneous
Original
Accurate
Complete
Consistent
Enduring
Available
4. What are IQ, OQ, and PQ?
IQ (Installation Qualification): Verifies correct installation.
OQ (Operational Qualification): Confirms equipment operates as intended.
PQ (Performance Qualification): Demonstrates consistent performance under actual conditions.
5. Why is Audit Trail Review important in Lab QA?
Audit trail review helps verify data integrity by tracking all changes made in computerized systems, ensuring compliance with regulatory requirements such as USFDA, MHRA, and WHO-GMP guidelines.
Conclusion
Ipca Laboratories Limited offers a promising opportunity for professionals in Engineering (QMS), Lab QA, and QC functions. Candidates with relevant pharmaceutical experience and knowledge of GMP, Data Integrity, Validation, and Laboratory Compliance are encouraged to apply and become part of a leading pharmaceutical organization.
Ipca Laboratories Limited Hiring– Engineering (QMS), Lab QA & QC Departments
The post Ipca Laboratories Limited Hiring– Engineering (QMS), Lab QA & QC Departments appeared first on The Jobs Post –Job Alerts for Freshers & Experts.
