India's DMPLOI - Jobs & Networking AppLincoln Pharmaceuticals Ltd., one of India’s leading pharmaceutical manufacturing companies, has announced a Walk-In Interview Drive on 14th June 2026 (Sunday) for multiple positions across Production, Quality Assurance, Quality Control, Warehouse, and Packing departments. This recruitment drive offers excellent career opportunities for experienced pharmaceutical professionals seeking growth in OSD and Injectable manufacturing operations.
The company is inviting qualified candidates with relevant experience to join its expanding operations at the Khatraj Unit, Gujarat.
Walk-In Interview Details
Company: Lincoln Pharmaceuticals Ltd.
Interview Date: 14th June 2026 (Sunday)
Time: 9:00 AM to 3:00 PM
Venue: Lincoln House, Behind Satyam Complex, Science City Road, Sola, Ahmedabad – 380060, Gujarat
Open Positions
1. Production – OSD & Injectable
Officer / Sr. Officer
Qualification: B.Pharm, B.Sc, M.Sc
Experience: 1 to 5 Years
OSD Sections:
Coating
Compression
Packing
Granulation
Ointment/External Preparation
General Manufacturing
Sterile Manufacturing
Injectable Sections:
Aseptic Processing
SIP/CIP Operations
Batch Manufacturing
Bulk Manufacturing
Dry Powder
Oral Liquid
2. Production – OSD & Injectable
Operator
Qualification: ITI, Diploma
Experience: 1 to 8 Years
OSD Sections:
Compression
Granulation
Coating
Capsule Filling
Ointment Manufacturing
Sterile Manufacturing
Tube Filling
Injectable Sections:
Mixing
Dry Powder Manufacturing
3. Warehouse
Officer / Sr. Officer
Qualification: B.Sc, M.Sc, B.Com, BBA
Experience: 1 to 5 Years
Section:
RM & PM Store Management
4. Packing – OSD
Operator
Qualification: ITI, Diploma
Experience: 1 to 5 Years
Section:
Auto Carton Machine
Strip Machine
Dry Syrup Machine
5. Quality Assurance (QA)
Officer / Sr. Officer / Executive
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
Experience: 1 to 7 Years
Key Areas:
IPQA
OSD & Injectable QA
AQA
APQR
Documentation
Validation
QMS
CQA
Artwork Management
Stability
6. Quality Control (QC)
Officer / Sr. Officer
Qualification: B.Sc, M.Sc, B.Pharm
Experience: 1 to 8 Years
Analytical Sections:
HPLC Operation & Calibration
Dissolution Testing
Assay & Related Substances
RM Testing by HPLC
GLP Compliance
Finished Product Analysis
Stability Studies
PM Laboratory Testing
Microbiology Section:
Microbiological Testing
Environmental Monitoring
Sterility Testing
Why Join Lincoln Pharmaceuticals?
Strong presence in domestic and international pharmaceutical markets.
Opportunities in both OSD and Injectable manufacturing facilities.
Exposure to cGMP-regulated manufacturing environments.
Career growth through advanced pharmaceutical technologies.
Professional work culture focused on quality and compliance.
Important Notes
Freshers are requested to email their CVs to hr@lincolnpharma.com and should not attend the walk-in interview.
Candidates who have attended an interview with Lincoln Pharmaceuticals within the last six months will not be considered.
Carry updated resume, educational certificates, experience documents, salary proof, and passport-size photographs.
Technical FAQs
1. What is the purpose of CIP and SIP in injectable manufacturing?
CIP (Clean-In-Place) is used to clean equipment without dismantling it, while SIP (Sterilize-In-Place) sterilizes equipment using steam. Both processes are critical for maintaining sterility and preventing contamination in injectable manufacturing.
2. Why is HPLC widely used in pharmaceutical quality control?
High-Performance Liquid Chromatography (HPLC) is used for assay, impurity profiling, stability testing, and raw material analysis because it provides high accuracy, sensitivity, and reproducibility.
3. What is IPQA and why is it important?
In-Process Quality Assurance (IPQA) involves monitoring manufacturing activities during production to ensure compliance with GMP requirements and product quality standards before batch release.
4. What is APQR in pharmaceutical quality systems?
Annual Product Quality Review (APQR) is a periodic review of manufacturing and quality data to evaluate product consistency, identify trends, and implement continuous improvement measures.
5. What are the critical parameters monitored during sterile manufacturing?
Key parameters include:
Differential pressure
Temperature and humidity
HEPA filter integrity
Viable and non-viable particle counts
Environmental monitoring results
Aseptic process compliance
These controls help ensure product sterility and patient safety.
Conclusion:
The Lincoln Pharmaceuticals Walk-In Interview on 14th June 2026 presents an excellent opportunity for pharmaceutical professionals with experience in Production, QA, QC, Warehouse, and Packing functions. Candidates possessing relevant qualifications and hands-on manufacturing experience are encouraged to attend the interview and explore rewarding career opportunities with a growing pharmaceutical organization.
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