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Hetero Labs Limited, a leading Indian pharmaceutical company founded in 1993, is hosting a walk-in interview for its manufacturing facilities in Hyderabad, Telangana. Renowned for producing high-quality generic medicines and APIs across 145+ countries, Hetero operates USFDA, EU-GMP, and WHO-GMP compliant plants.
Rated 3.8/5 on AmbitionBox for job security, we invite professionals with 2–9 years of experience to join our team of 10,000+ employees to drive excellence in OSD and injectable formulations.
Walk-In Interview Details
- Date: Sunday, July 6, 2025
- Time: 9:00 AM to 4:00 PM
- Venue: Kyriad Hotel Indore, Plot 34-35, FF Scheme No. 54, Opposite Meghdoot Garden, Vijay Nagar, Indore, Madhya Pradesh – 452010
- Work Location: Hetero Labs Limited, Hyderabad, Telangana (specific units: Jeedimetla, Jadcherla, or similar)
Contact:
- Email resumes to Prashanthkumar.v@hetero.com
- Call +91 9010203989 or +91 8555912639 for inquiries
Required Documents:
- Updated resume (2 copies)
- Original and photocopies of educational certificates (ITI/Diploma/B.Sc/B.Pharm/M.Sc/M.Pharm)
- Last 3 months’ payslips and latest CTC particulars
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Candidates must have 2–9 years of experience in OSD or injectable formulations and exposure to USFDA/EU-GMP approved plants.
- Candidates interviewed at Hetero in the last 6 months are ineligible.
- Willingness to work in shift operations is required.
- Spot offers may be provided subject to document verification.
Open Positions
Production (OSD)
- Designation: Operator / Senior Operator / Officer
- Qualification: ITI / Diploma / B.Sc / B.Pharm
- Experience: 2–7 years
- Vacancies: Multiple (exact number TBD)
Area of Work:
- Operate and troubleshoot equipment for compression, coating, granulation, inspection, and capsule filling.
- Ensure compliance with cGMP, SOPs, and safety standards.
- Support BMR/BPR documentation and regulatory audits (USFDA, EU-GMP).
Key Skills:
- Hands-on experience with OSD equipment (e.g., RMG, FBP, tablet press).
- Knowledge of cGMP, SOPs, and audit compliance.
Production (Injectable)
- Designation: Operator / Senior Operator / Officer / Junior Executive
- Qualification: ITI / Diploma / B.Sc / B.Pharm / M.Sc
- Experience: 2–7 years
- Vacancies: Multiple (exact number TBD)
Area of Work:
- Manage filling and sealing, lyophilizer, visual inspection, autoclave, and vial washing operations.
- Handle QMS activities, deviations, and compliance for audits.
- Ensure aseptic practices and adherence to cGMP standards.
Key Skills:
- Expertise in injectable manufacturing and aseptic processes.
- Knowledge of cGMP, QMS, and regulatory audits (USFDA, EU-GMP).
Quality Control (OSD)
- Designation: Junior Executive / Executive / Senior Executive
- Qualification: B.Pharm / M.Sc / M.Pharm
- Experience: 2–9 years
- Vacancies: Multiple (exact number TBD)
Area of Work:
- Perform IP/FP, stability, method transfer, and method development using HPLC, GC, and other analytical instruments.
- Conduct analytical testing and validation per GLP standards.
- Support regulatory audits with accurate documentation.
Key Skills:
- Proficiency in HPLC, GC, and analytical method development.
- Knowledge of cGMP, GLP, and regulatory compliance (USFDA, EU-GMP).
Quality Assurance (Injectable)
- Designation: Officer / Junior Executive / Executive / Senior Executive
- Qualification: B.Pharm / M.Sc / M.Pharm
- Experience: 2–9 years
- Vacancies: Multiple (exact number TBD)
Area of Work:
- Conduct validation, IPQA, QMS, equipment qualification, and compliance activities for QC and microbiology.
- Review BMR/BPR, manage deviations, CAPA, and change control.
- Ensure compliance with cGMP and regulatory standards (USFDA, EU-GMP).
Key Skills:
- Expertise in IPQA, QMS, and validation for injectables.
- Strong documentation and audit readiness skills.
Why Join Hetero Labs?
- Global Leader: Contribute to a company with a $2 billion revenue (FY 2024), exporting generics and APIs to 145+ countries, including anti-retroviral drugs for HIV/AIDS.
- Regulatory Excellence: Work in USFDA, EU-GMP, and WHO-GMP compliant facilities, with 300+ ANDAs and 25+ EDMFs filed.
- Supportive Culture: Rated 3.8/5 on AmbitionBox for job security and teamwork, though work-life balance is moderate at 3.5/5 due to shift demands.
- Innovation Hub: Join Hyderabad’s thriving pharma ecosystem, with Hetero’s facilities leading in OSD and injectable production.
How to Apply
- Walk-In: Attend the interview on July 6, 2025, at Kyriad Hotel Indore with all required documents.
- For Those Unable to Attend: Email your updated CV to Prashanthkumar.v@hetero.com, mentioning the specific role and department (e.g., “Production Officer – OSD” or “QA Executive – Injectable”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.
Note: Candidates with USFDA/EU-GMP approved plant experience are preferred.
About Hetero Labs
Founded in 1993, Hetero Labs Limited is a Hyderabad-based global pharmaceutical company with 36 manufacturing facilities, including key units in Jeedimetla and Jadcherla.
Specializing in generics, APIs, and biosimilars, Hetero is a world leader in anti-retroviral drugs and serves regulated markets with 300+ ANDAs. With 1,200+ scientists in R&D, Hetero drives innovation and quality in OSD and injectable formulations. Learn more at www.hetero.com.
Important Disclaimer
Hetero Labs Limited does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers to hrd@hetero.com.
Join Hetero Labs and contribute to high-quality pharmaceutical manufacturing in Hyderabad!