ALKEM Laboratories Walk-In Drive Indore for QA, QC, and Production

Career with ALKEM Laboratories – Walk-In Interview in Indore!
ALKEM Laboratories, a leading global pharmaceutical company, is conducting a walk-in interview for various positions in the QA, QC, and Production departments. This exciting opportunity is set for February 23, 2025, at the Hotel Red Maple in Indore, Madhya Pradesh. If you’re looking to advance your career in the pharmaceutical manufacturing industry, this could be your perfect chance!
Current Vacancies at ALKEM Laboratories Indore Facility
- QA (Quality Assurance)
- QC (Quality Control)
- Production
These positions are available at ALKEM’s Formulation Manufacturing Facility based in Daman. The walk-in drive is specifically targeting candidates who possess a solid foundation in pharmaceutical manufacturing processes and quality control.
Educational Qualifications Required for ALKEM Laboratories Walk-In Drive
- M.Sc. in Pharmaceutical Sciences
- M.Pharm in Pharmaceutical Sciences
- B.Pharm in Pharmacy
- Diploma in Pharmacy
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📱 Join Click HereThe ideal candidate will hold one of these qualifications along with the relevant professional experience to contribute to ALKEM’s high standards of pharmaceutical manufacturing.
Experience Requirements for the Positions
The walk-in drive offers various positions for experienced professionals. Below are the key experience requirements:
- Quality Assurance (QA): 3 to 7 years of experience in handling CAPA, internal/external audits, and process validation.
- Quality Control (QC): 2 to 6 years of experience with analytical instrumentation (HPLC, UV, Dissolution), review of equipment audit trails, and BMR/BPR review.
- Production: 2 to 7 years of experience in the manufacturing core area, handling processes like liquid, tablets, capsules, and solid dosage forms.
Key Responsibilities of QA, QC, and Production Roles at ALKEM Laboratories
QA (Quality Assurance):
- Overseeing quality control measures and ensuring compliance with GMP standards.
- Managing external audits, including USFDA, MHRA, and German regulatory inspections.
- Process validation, equipment qualification, and handling CAPA (Corrective and Preventive Actions).
QC (Quality Control):
- Operating analytical instruments like HPLC, UV, and dissolution testing for raw materials and finished products.
- Performing batch record reviews (BMR/BPR) and line clearance checks.
- Ensuring compliance with regulatory standards for product testing and quality assurance.
Production:
- Managing operations on the shop floor, including liquid, tablet, and capsule manufacturing.
- Handling equipment like Glatt Granulation, compression machines, and capsule filling machines.
- Involved in the production of blister and bulk packaging for pharmaceutical products.

Documents to Carry at the Venue
Please ensure to carry the following documents to the interview:
- Updated Resume with detailed contact information.
- CTC Structure and Increment/Revision Letter from the current employer.
- Passport Photo for identification.
- Aadhar and PAN Card for verification purposes.
Event Details:
- Date: February 23, 2025 (Sunday)
- Venue: Hotel Red Maple, Jhoomer Ghat, Rasalpura, Rau, Indore, Madhya Pradesh, Pin Code: 453446.
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