Ajanta Pharma Walk-In Interview for Manufacturing, Packing & Quality Control Roles in Indore – May 11, 2025

Join Ajanta Pharma Limited, a Great Place to Work® Certified (Feb 2025–Feb 2026) specialty pharmaceutical company, at our Walk-In Interview on May 11, 2025, in Indore for Manufacturing, Packing, and Quality Control (QC) roles at our USFDA-approved formulation facility in Dahej, Bharuch, Gujarat.

With operations in 30+ countries and 7 state-of-the-art manufacturing facilities, Ajanta is a leader in oral solid dosage (OSD) formulations, generating ₹4,200 Crore revenue (FY24). Rated 3.9/5 for job security on AmbitionBox (2,800+ reviews), salaries range from ₹2.5–8 Lakhs/year (Glassdoor). Be part of our mission to Serve Health Care Needs Worldwide!

Walk-In Interview Details

• Date: Sunday, May 11, 2025
• Time: 9:00 AM – 5:00 PM
• Venue: Papaya Tree Hotel, A.B. Road, Near Dr. Hardia Eye Clinic, Rau, Indore, Madhya Pradesh 453331
• Work Location: Ajanta Pharma Limited, Plot No. Z-103/I, SEZ Phase-II, Dahej, Bharuch, Gujarat 392130
• Application: Walk-in with documents or email CV to referral.dhj@ajantapharma.com, subject: “[Position] – Dahej, May 2025.”
• Contact: +91-22-6606-1000, referral.dhj@ajantapharma.com
• Website: www.ajantapharma.com
• Transport: AC bus provided from Bharuch/Vadodara to Dahej plant.

Notes:

• Fraud Alert: Ajanta does not charge fees or request banking details. Verify via sanketa.pednekar@ajantapharma.com or www.ajantapharma.com.

Why Ajanta Pharma?

Ajanta’s Dahej facility is USFDA and MHRA-approved, specializing in OSD formulations (tablets, capsules) for cardiology, dermatology, and ophthalmology. With 170+ ANDAs and a focus on first-to-market products, Ajanta drives innovation. Rated 3.8/5 for skill development (Indeed), it offers robust training but scores 3.6/5 for career growth due to competitive promotions. Benefits include health insurance, transport, and canteen.

The roles align with India’s $24.4 billion pharma export market (10% CAGR, Invest India). Ajanta’s 2024 leadership in anti-malarial generics and recent USFDA approvals highlight its global impact.

Job Positions

1. Manufacturing/Packing – Associate/Operator

• Qualification: 10th, 12th + ITI (AOCP, MMCP), Diploma (Mechanical, Chemical), D.Pharm
• Experience: 2–10 years in OSD formulations
• Vacancies: ~10–15 (estimated)
• Skills:
  • Manufacturing: Granulation (RMG, FBE), pellet coating (Wurster), capsule filling (AF-90T, Zanasi), compression (Fette, Korsch).
  • Packing: Primary (blister packing, sachet filling, bottle/bulk packing), secondary (cartonator, labeling, Track & Trace).
  • Knowledge of cGMP, SOPs, and regulatory audits (USFDA, MHRA).
• Tasks: Operate manufacturing/packing equipment, ensure compliance, maintain BMR/BPR, support audits.
• Why Join?: Hands-on OSD expertise for global markets; 80% tasks support regulatory compliance.

2. Manufacturing/Packing – Sr. Officer/Officer

• Qualification: B.Pharm, M.Pharm
• Experience: 2–8 years in OSD formulations
• Vacancies: ~5–8
• Skills:
  • Manufacturing: Compression, pellet coating, capsule filling.
  • Packing: Primary/secondary packing, Track & Trace.
  • Expertise in e-BPR, e-log, cGMP, and USFDA/MHRA audits.
• Tasks: Supervise production/packing, troubleshoot processes, manage electronic records, ensure audit readiness.
• Why Join?: Lead OSD operations with digital tools for regulated markets.

3. Quality Control (QC) – Sr. Officer/Officer

• Qualification: B.Sc (Chemistry), M.Sc (Chemistry), B.Pharm, M.Pharm
• Experience: 2–8 years in OSD QC
• Vacancies: ~5–8
• Skills:
  • Analysis of finished products, in-process, or stability samples using HPLC, UV spectrophotometer, dissolution tester.
  • Experience in analytical method validation/transfer (ICH Q2).
  • Operation of GC, ICPMS, or LCMS (preferred).
  • Knowledge of GLP, QMS, and OOS/OOT investigations.
• Tasks: Conduct sample analysis, validate methods, manage lab instruments, support regulatory audits.
• Why Join?: Master analytical techniques for USFDA-compliant OSD products.

Who Can Apply?

• Qualifications: 10th, 12th, ITI, Diploma, D.Pharm, B.Sc, M.Sc, B.Pharm, M.Pharm.
• Experience: 2–10 years in OSD manufacturing, packing, or QC with USFDA/MHRA exposure.
• Key Skills:
  • Manufacturing/Packing: Granulation, compression, coating, capsule filling, blister/bottle packing, Track & Trace, e-BPR/e-log.
  • QC: HPLC, UV, dissolution testing, method validation, GC/ICPMS/LCMS, GLP.
  • Strong documentation and shift adaptability (A/B/C).
• Preferred: Experience with Fette/Korsch (compression), Wurster coaters, or Chromeleon software; audit-facing roles.

How to Prepare

1. Bring Documents: CV (highlight USFDA/MHRA experience), mark sheets (10th, 12th, ITI/Diploma/Degree), degree certificate, experience letters, CTC breakup, last 3 months’ payslips, Aadhaar/PAN copies, passport-size photo.
2. Dress Smart: Formal attire (shirt, trousers; avoid casuals).
3. Study Up:
   • Manufacturing/Packing: Review granulation (e.g., RMG parameters), compression (e.g., tooling issues), pellet coating, blister packing, Track & Trace, e-BPR. Prepare examples (e.g., “How did you resolve a coating defect?”).
   • QC: Study HPLC method validation, dissolution testing, OOS/OOT handling, and ICH Q2. Discuss lab experience (e.g., “How did you troubleshoot an HPLC peak?”).
   • Research Ajanta’s Dahej facility and OSD portfolio (e.g., anti-malarials, dermatology). Visit www.ajantapharma.com.
   • Address shift concerns diplomatically (28% rate work-life balance low, AmbitionBox).
4. Arrive Early: 8:30 AM for registration; expect 1–2 hour wait (AmbitionBox). Public transport (Indore BRTS) to Rau; parking available.
5. Interview: Expect technical (65%) and behavioral (35%) questions; emphasize regulatory exposure.

Why Dahej, Gujarat?

Ajanta’s Dahej facility, located in SEZ Phase-II, is part of Gujarat’s $7 billion pharma sector (12% CAGR, Invest India). Just 40 km from Bharuch via NH-48, it offers 300+ pharma jobs (Naukri) and affordable living (₹10,000/month for 1BHK, AmbitionBox). AC bus transport from Bharuch/Vadodara ensures connectivity. Ideal for regulatory-focused OSD careers.

Contact Information

• Email: referral.dhj@ajantapharma.com (Applications), sanketa.pednekar@ajantapharma.com (Verification)
• Phone: +91-22-6606-1000 (Corporate Office)
• Venue: Papaya Tree Hotel, A.B. Road, Near Dr. Hardia Eye Clinic, Rau, Indore, Madhya Pradesh 453331
• Work Location: Ajanta Pharma Limited, Plot No. Z-103/I, SEZ Phase-II, Dahej, Bharuch, Gujarat 392130
• Corporate Office: Ajanta Pharma Limited, Ajanta House, 98 Govt Industrial Area, Charkop, Kandivli (West), Mumbai, Maharashtra 400067
• Connect: LinkedIn, Facebook
• Website: www.ajantapharma.com

Apply Now for Ajanta Pharma’s Walk-In on May 11, 2025, in Indore to join a USFDA-approved leader in Dahej, Gujarat!