Alkem Laboratories Limited, one of India’s leading pharmaceutical companies, has announced a Walk-In Interview for experienced professionals at its Formulation Manufacturing Facility in Daman. The recruitment drive offers opportunities in Quality Control (QC), Production Formulation, and Production Packing departments.
Candidates with relevant pharmaceutical manufacturing experience are invited to attend the interview with all required documents.
Walk-In Interview Details
Particular Details
Company
Alkem Laboratories Limited
Industry
Pharmaceutical – Formulation Manufacturing
Job Type
Walk-In Interview
Interview Date
19th July 2026 (Sunday)
Interview Time
09:00 AM to 03:30 PM
Facility Location
Daman Formulation Manufacturing Facility
Interview Venue
Hotel Woodland (Vapi), NH No. 8, Near Desai Auto Mobiles, Balitha, Vapi, Gujarat
Department-wise Vacancy Details
1. Quality Control (QC) – Formulation
Position
Officer
Senior Officer
Qualification
M.Sc.
B.Pharm
Experience
2 to 7 Years
Required Technical Skills
Finished Product (FP) Analysis
Stability Testing
HPLC Operation
UV Spectrophotometer
Dissolution Testing
Analytical Instrumentation
LIMS
Empower Software (Waters)
2. Production – Formulation
Position
Technical Associate
Qualification
Diploma
B.Sc.
ITI
Experience
2 to 6 Years
Manufacturing Expertise Required
Wurster (Glatt, 21 CFR SCADA)
Pellet Coating
Bottom Spray (Glatt)
Granulation (Integrated Line, GEA/Glatt)
Flow Coater
Compression (KORSCH, SEJONG, GEA, CADMACH)
Coating (Glatt Coater)
Liquid Manufacturing
Liquid Filling
Capsule Manufacturing
Sachet Filling Machines (Wraptech/Bossar)
3. Production (Packing)
Positions
Officer
Senior Officer
Technical Associate
Qualification
B.Pharm
Diploma
B.Sc.
ITI
Experience
2 to 6 Years
Primary Packing Expertise
Blister Packing (Uhlmann, Elmach, BQS)
Bulk Packing
Bottle Packing
CVC Machines
Liquid Packing
Documents Required
Candidates should carry:
Updated Resume
Passport Size Photograph
Salary Breakup
Latest Increment Letter
Aadhaar Card Copy
PAN Card Copy
Why Join Alkem Laboratories?
One of India’s leading pharmaceutical companies
Great Place to Work Certified
Modern formulation manufacturing facility
Career growth opportunities
Exposure to advanced pharmaceutical manufacturing technologies
Professional and GMP-compliant work environment
Selection Process
Walk-In Registration
Document Verification
Technical Interview
HR Discussion
Final Selection
Important Instructions
Reach the venue before the reporting time.
Carry all original documents along with photocopies.
Bring multiple copies of your updated resume.
Candidates with relevant formulation manufacturing experience will be preferred.
Dress professionally for the interview.
Conclusion
This Alkem Laboratories Walk-In Interview 2026 is an excellent opportunity for experienced pharmaceutical professionals looking to advance their careers in Quality Control, Production, and Packing. Candidates possessing the required qualifications and technical expertise are encouraged to attend the interview on 19th July 2026 in Vapi, Gujarat.
Technical FAQs
1. Which analytical instruments should QC candidates be familiar with?
Candidates should have hands-on experience with HPLC, UV Spectrophotometer, Dissolution Testing, Stability Testing, LIMS, and Waters Empower software.
2. What manufacturing equipment experience is expected for Production roles?
Experience with Glatt Wurster systems, GEA Granulation, KORSCH/SEJONG/CADMACH Compression machines, Flow Coaters, Capsule Manufacturing, and Sachet Filling machines is preferred.
3. Which packing machines are used in the Packing department?
Candidates should have knowledge of Uhlmann, Elmach, BQS blister packing machines, CVC bottle packing systems, bulk packing, and liquid packing operations.
4. Is pharmaceutical manufacturing experience mandatory?
Yes. The advertised positions require 2–7 years of relevant experience in formulation manufacturing, quality control, production, or packing, depending on the role.
5. What GMP knowledge is expected from candidates?
Candidates should be familiar with Good Manufacturing Practices (GMP), SOP compliance, documentation practices, safety procedures, equipment operation, and quality standards followed in pharmaceutical manufacturing.



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