Ipca Laboratories Hiring 2026 – Quality Control Jobs in Gujarat
Ipca Laboratories Limited has announced an opportunity for experienced professionals in its Quality Control (QC) department at Gandhidham, Gujarat.
The opening is aimed at candidates who have solid experience in pharmaceutical QC laboratories and are comfortable handling analytical testing, investigations, documentation, compliance systems and laboratory operations.
If you have 7–10 years of relevant pharmaceutical QC experience, this could be a good opportunity to take the next step in your career.
Job Overview
| Details | Information |
|---|---|
| Company | Ipca Laboratories Limited |
| Department | Quality Control (QC) |
| Position | Executive / Senior Executive |
| Experience | 7–10 Years |
| Qualification | B.Pharm / M.Pharm / B.Sc / M.Sc |
| Location | Gandhidham, Gujarat |
| Industry | Pharmaceutical |
| Work Type | Full-Time / On-site |
| Application Mode |
Position: Executive / Senior Executive – Quality Control
The selected professional will be responsible for supporting QC laboratory activities while maintaining strong standards for testing, documentation, investigation and regulatory compliance.
The role combines technical laboratory knowledge with experience in quality systems and team coordination.
Major Areas of Work
- Quality Control laboratory operations
- Analytical testing and review
- Investigation and deviation handling
- CAPA management
- Change control
- SOP preparation
- Data review and GLP compliance
- QC instrument calibration
- Team and manpower planning
Eligibility Criteria
Candidates should have:
- B.Pharm / M.Pharm / B.Sc / M.Sc qualification
- 7–10 years of relevant experience in pharmaceutical Quality Control
- Strong experience working in a pharmaceutical QC laboratory
- Good knowledge of analytical instruments and QC systems
- Experience with investigations and quality documentation
Freshers are not eligible for this particular opening.
Technical Skills Required
Candidates should be familiar with pharmaceutical analytical testing and laboratory equipment, including:
- HPLC
- GC
- UV Spectrophotometer
- IR
- Disintegration Test (DT)
- Dissolution testing
- QC instrument calibration
Experience in troubleshooting and maintaining analytical equipment will be valuable for this position.
Quality & Compliance Skills
The role also requires practical experience in:
- CAPA
- Deviation management
- Change control
- Root Cause Analysis (RCA)
- Investigation handling
- SOP preparation and drafting
- Training management
- Data review
- GLP practices
- Manpower planning
These skills are particularly important for professionals working in regulated pharmaceutical QC environments.
Software Knowledge
Experience with pharmaceutical quality and laboratory systems is expected.
Useful software knowledge includes:
- TrackWise
- EDMS
- LMS
- LIMS
Familiarity with electronic documentation and laboratory management systems can be an advantage when handling QC workflows and compliance activities.
Key Responsibilities
Depending on the assigned responsibilities, the selected candidate may be involved in:
- Managing day-to-day QC laboratory activities
- Reviewing analytical test results
- Handling deviations and investigations
- Preparing and monitoring CAPA
- Supporting change-control activities
- Conducting root-cause analysis
- Preparing and updating SOPs
- Reviewing QC documentation
- Ensuring GLP and data-integrity practices
- Managing QC instrument calibration activities
- Planning laboratory manpower and work allocation
- Supporting training activities
- Working with laboratory software such as LIMS and TrackWise
- Supporting audit and inspection readiness
Why Consider This Opportunity?
For experienced QC professionals, the role offers an opportunity to work in a structured pharmaceutical environment and take on responsibilities beyond routine testing.
You can gain exposure to:
- Advanced QC laboratory operations
- Pharmaceutical quality systems
- Investigations and CAPA
- Regulatory compliance
- Laboratory management
- Team coordination and training
The experience can also support future progression toward senior QC and managerial positions.
How to Apply
Interested and eligible candidates should send their updated CV by email.
Email: shivendrav.singh@ipca.com
Work Location: Gandhidham, Gujarat
Before applying, make sure your resume clearly highlights your QC experience, analytical instrument knowledge, investigation experience, quality systems and software expertise.
Important Eligibility Note
This is an experienced-level QC opportunity.
Candidates should have 7–10 years of relevant pharmaceutical Quality Control experience. Fresh graduates and candidates without the required experience should not apply for this particular position.
Frequently Asked Questions
1. Who can apply for Ipca Laboratories QC jobs?
Candidates with B.Pharm, M.Pharm, B.Sc or M.Sc qualifications and 7–10 years of relevant pharmaceutical QC experience can apply.
2. Are freshers eligible for this position?
No. This particular Executive/Senior Executive QC opening requires substantial relevant experience.
3. Where is the job located?
The position is based at Gandhidham, Gujarat.
4. What analytical instruments should candidates know?
Candidates should have experience or knowledge of HPLC, GC, UV, IR, disintegration and dissolution testing, along with QC instrument calibration.
5. What quality-system experience is useful?
Experience with CAPA, deviations, change control, RCA, investigations, SOP preparation, GLP and data review is important.
6. Which software knowledge is preferred?
Candidates should be familiar with systems such as TrackWise, EDMS, LMS and LIMS.
7. How can I apply?
Send your updated CV to shivendrav.singh@ipca.com and mention the relevant QC position in your application.
