Mankind Pharma is conducting a Mega Walk-In Drive for experienced Quality Control (QC) and Quality Assurance (QA) professionals. The hiring drive offers opportunities across API, Formulation, OSD, Injectables, and Ophthalmic manufacturing facilities located in Rajasthan and Himachal Pradesh.
Candidates with experience in regulated pharmaceutical environments and exposure to USFDA/MHRA standards are encouraged to participate. This is an excellent opportunity for professionals seeking career growth in pharmaceutical quality assurance and quality control functions.
Walk-In Interview Details
Date: 31st May 2026 (Sunday)
Time: 09:30 AM to 04:00 PM
Venue:
Sayaji Hotel
H-1, Scheme No. 54, Vijay Nagar,
Indore – 452010, Madhya Pradesh
Available Positions
1. API Unit-1, Behror (Rajasthan)
Quality Control
Experience: 2+ Years
Qualification: B.Sc / M.Sc (Chemistry) / B.Pharm
Key Skills
- HPLC & GC operation using Empower software
- Wet lab analysis
- UV, IR, SOR, LOD, Assay
- KFT, Bulk Density, PSD, Surface Area analysis
- Advanced instrument handling including LC-MS
Quality Assurance
Experience: 2+ Years
Qualification: M.Sc (Chemistry) / B.Pharm / M.Pharm
Key Skills
- Process validation
- Technology transfer
- Change control management
- CAPA handling
- Audit trail review
- SAP knowledge
- Documentation compliance
2. Formulation Plant Unit-2, Paonta Sahib (Himachal Pradesh)
Raw Material Quality Control (RM QC)
Experience: 2–8 Years
Qualification: M.Sc / B.Pharm / M.Pharm
Key Skills
- Raw material sampling and inspection
- Incoming material testing
- HPLC analysis
- OOS/OOT investigations
- Documentation and calibration
Finished Goods Quality Control (FG QC)
Experience: 2+ Years
Qualification: M.Sc / B.Pharm
Key Skills
- Finished product testing
- HPLC analysis
- Stability studies
- Shelf-life analysis
- Product release documentation
3. Formulation Plant Unit-3, Paonta Sahib (OSD, Injectables & Ophthalmic)
Quality Control Officer
Experience: 2–5 Years
Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)
Instrument Knowledge
- AAS
- LC-MS
- GC-MS
- IC
- GCHS
- UV
- HPLC
Exposure Required
- Raw Material Analysis
- Finished Product Testing
- Stability Analysis
Quality Assurance Officer (IPQA/QMS)
Experience: 2–5 Years
Qualification: B.Pharm / M.Pharm
Key Responsibilities
- IPQA activities
- QMS management
- GMP compliance monitoring
- Documentation review
- Process monitoring
Key Responsibilities
- Perform pharmaceutical quality control testing.
- Conduct HPLC, GC, LC-MS and analytical instrument operations.
- Execute IPQA and QMS activities.
- Manage CAPA, change controls, and audit compliance.
- Review batch records and quality documentation.
- Support regulatory compliance and validation activities.
- Participate in investigations including OOS and OOT events.
- Ensure adherence to GMP, GLP and data integrity requirements.
Required Qualifications
- B.Sc (Chemistry)
- M.Sc (Chemistry)
- B.Pharm
- M.Pharm
Preferred Candidates
- Experience in USFDA or MHRA regulated manufacturing facilities.
- Himachal Pradesh domicile candidates preferred for Unit-2 and Unit-3 positions.
- Strong analytical and documentation skills.
Benefits
- Opportunity to work with one of India’s leading pharmaceutical companies.
- Exposure to regulated manufacturing environments.
- Career growth in API, OSD, Injectables, and Ophthalmic segments.
- Hands-on experience with advanced analytical instruments.
- Competitive salary and employee benefits.
- Learning opportunities in quality systems and regulatory compliance.
How to Apply
Eligible candidates can directly attend the walk-in interview at the specified venue.
Contact Details
Email: sandeep.bhadana@mankindpharma.com
