Hetero, one of India’s leading pharmaceutical companies, has announced a Talent Drive for its API Division to recruit talented professionals across multiple departments. The company is offering opportunities for freshers and experienced candidates at its manufacturing facilities located in Hyderabad and Vizag. Immediate joiners in QC, QA, and Production departments are eligible for a joining bonus.
This walk-in recruitment drive provides candidates with the opportunity to receive an offer letter on the spot after successful interview rounds.
About Hetero
Hetero is a globally recognized pharmaceutical organization specializing in APIs, generics, biosimilars, and custom pharmaceutical services. The company operates state-of-the-art manufacturing facilities and supplies healthcare products to numerous international markets.
Available Departments and Roles
1. Production
Role: Chemist / Executive
Qualification: B.Sc / M.Sc
Experience: 0–8 Years
2. Quality Control (QC)
Role: HPLC, GC, Wet Lab, Microbiology
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 0–8 Years
3. Quality Assurance (QA)
Role: AQA, IPQA, QMS, Documentation
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 0–8 Years
4. Engineering Services
Role: Maintenance, Electrical, Civil
Qualification: B.Tech / Diploma
Experience: 3–8 Years
5. EHS (Environment, Health & Safety)
Role: Process Safety & Environmental
Qualification: B.Tech (Chemical) / Diploma
Experience: 3–6 Years
6. TSD (Technical Services Department)
Role: Process Engineering
Qualification: B.Tech (Chemical)
Experience: 3–6 Years
Walk-In Interview Details
Interview Dates: 13th & 14th June 2026
Time: 09:00 AM – 04:30 PM
Venue:
Hotel Sitara Grand,
Opp. Srinivasa Theatre, Chanda Nagar,
Hyderabad – 502032
Contact Persons:
Kiran Kumar S – 8977524947
Anil – 8977539379
Documents Required
Candidates should carry:
Updated Resume
Educational Certificates
Latest Increment Letter
Last 3 Months’ Salary Slips
Last 6 Months’ Bank Statements
Passport Size Photographs
Aadhaar Card Copy
Why Join Hetero?
Opportunity to work with a leading pharmaceutical manufacturer
Openings for both freshers and experienced professionals
Multiple career paths across Production, Quality, Engineering, and Safety
Immediate joining opportunities
Spot offer letters for selected candidates
Exposure to advanced API manufacturing technologies
Selection Process
The recruitment process may include:
Resume Screening
Technical Interview
HR Discussion
Document Verification
Offer Letter Issuance for selected candidates
Important Recruitment Notice
Hetero conducts recruitment only through official channels and does not authorize any third-party agencies for hiring. Candidates should be cautious of fraudulent recruitment activities and contact the company through official communication channels for verification.
Technical FAQs
1. What is the role of HPLC in Quality Control laboratories?
HPLC (High Performance Liquid Chromatography) is used to identify, quantify, and analyze pharmaceutical compounds, impurities, and degradation products to ensure product quality and compliance with regulatory specifications.
2. What are the key responsibilities of an IPQA professional?
An IPQA professional monitors manufacturing activities, verifies compliance with SOPs, reviews batch records, performs line clearances, and ensures adherence to GMP requirements during production.
3. Why is process safety important in API manufacturing?
Process safety helps prevent chemical accidents, explosions, toxic releases, and operational hazards by implementing risk assessments, safety protocols, and engineering controls.
4. What is the significance of GC analysis in pharmaceutical laboratories?
Gas Chromatography (GC) is primarily used for residual solvent analysis, volatile compound testing, and impurity profiling as per pharmacopeial and regulatory requirements.
5. What does a Process Engineer do in the TSD department?
A Process Engineer optimizes manufacturing processes, improves production efficiency, supports technology transfer, investigates process deviations, and ensures consistent product quality during scale-up and commercial manufacturing.


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