Hetero Pharma, one of India’s leading pharmaceutical companies, has announced exciting career opportunities for candidates looking to build a successful career in the pharmaceutical industry. The company is currently recruiting for two positions at its Hyderabad facilities: Trainee – QC Sampling and Regulatory Affairs Specialist.
These openings provide excellent opportunities for freshers as well as experienced pharmaceutical professionals. Candidates with qualifications such as Intermediate, B.Pharm, M.Pharm, and M.Sc can apply based on the role requirements.
Hetero Pharma Recruitment 2026 – Job Overview
Company Name: Hetero Pharma
Job Locations:
• Hyderabad
• Jeedimetla, Hyderabad
Available Positions:
• Trainee – QC Sampling
• Regulatory Affairs Specialist
Employment Type:
Full-Time
Number of Vacancies:
Not Disclosed
Position 1: Trainee – QC Sampling
Department:
Quality Control
Job Location:
Hyderabad
Experience:
Freshers Preferred (2022–2026 Batch)
Qualification:
• Intermediate (MPC / BiPC)
Age Criteria:
• 18 to 25 Years
Job Purpose
The selected candidates will perform sampling activities according to approved procedures while ensuring compliance with cGMP, safety, and quality standards. The role supports quality control testing activities within the manufacturing facility.
Key Responsibilities
• Perform sampling of Raw Materials (RM), Packing Materials (PM), Intermediates, and Finished Products as per SOPs.
• Verify material labels, batch numbers, and container integrity before sampling.
• Maintain cleanliness of sampling booths, tools, and accessories.
• Transfer sampled materials to the QC laboratory.
• Complete sampling records, logbooks, and documentation accurately.
• Follow Good Documentation Practices (GDP).
• Adhere to cGMP, SOPs, and safety guidelines during all sampling activities.
Position 2: Regulatory Affairs Specialist
Department:
Regulatory Affairs
Work Location:
Jeedimetla, Hyderabad
Experience:
3 to 9 Years
Qualification:
• M.Pharm
• B.Pharm
• M.Sc
Market Exposure:
ROW, EU, and US Markets
Job Responsibilities
• Preparation, review, and submission of regulatory dossiers.
• Handle Life Cycle Management activities.
• Manage Post Approval and Pre Approval regulatory activities.
• Support MAA (Marketing Authorization Application) submissions.
• Ensure compliance with CMC documentation requirements.
• Coordinate with cross-functional teams for regulatory submissions and approvals.
Required Skills
• Strong understanding of global regulatory guidelines.
• Knowledge of dossier compilation and submission.
• Experience in pharmaceutical regulatory documentation.
• Excellent communication and coordination skills.
• Understanding of EU, US, and ROW regulatory requirements.
Salary and Benefits
Expected Salary Range
Trainee – QC Sampling:
₹1.8 LPA – ₹3.0 LPA
Regulatory Affairs Specialist:
₹6.0 LPA – ₹12.0 LPA
Benefits
• Competitive compensation package
• Career growth opportunities
• Exposure to global pharmaceutical markets
• Learning and development programs
• Professional work environment
• Employee welfare and healthcare benefits
Selection Process
• Application Screening
• Technical Evaluation
• HR Interview
• Final Selection
How to Apply
For Trainee – QC Sampling:
Interested candidates can apply through Hetero Pharma’s recruitment channels and official hiring drives.
For Regulatory Affairs Specialist:
Eligible candidates should send their updated CV to:
Subject Line:
Application for RA
