HETERO- HIRING FRESHERS – REGULATORY AFFAIRS

Pharmaguidances; Hyderabad; On-site; INR 300,000 - 420,000; Full time

Job summary

Hetero is seeking enthusiastic freshers to join its Regulatory Affairs team in Hyderabad. The role offers an entry-level path within a global API and generics company.

Location is Hyderabad with interview in Hyderabad. Required qualifications include M.Sc in Organic Chemistry or Biochemistry, or M.Pharmacy in Regulatory Affairs. Candidates should have basic regulatory knowledge and strong documentation skills.

Qualifications

• Basic knowledge of pharmaceutical regulatory requirements.
• Good communication and documentation skills.
• Attention to detail and analytical thinking.
• Ability to work effectively in a team.
• Proficiency in MS Office tools.

Responsibilities

• Prepare, review, and compile regulatory documents and dossiers.
• Coordinate with R&D, QA, QC, and Production teams.
• Maintain regulatory databases and documentation records.
• Ensure compliance with regulatory guidelines and company standards.
• Review labeling, packaging, and artwork for regulatory compliance.

Skills

Basic regulatory knowledge

Communication skills

Attention to detail

Teamwork

MS Office

Education

M.Sc. Organic Chemistry

M.Sc. Biochemistry

M.Pharmacy (Regulatory Affairs)

Job description

HETERO- HIRING FRESHERS – REGULATORY AFFAIRS

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector. We endeavour to serve patients by moulding science and technology into therapies to improve health outcomes and people’s lives.

HETERO IS HIRING | FRESHERS – REGULATORY AFFAIRS

Hetero is looking for enthusiastic, detail-oriented, and motivated freshers to join our Regulatory Affairs Team in Hyderabad.

Job Location : Hyderabad

Interview Location : Hyderabad

Department : Regulatory Affairs

Preferred Qualifications

• M.Sc. Organic Chemistry
• M.Sc. Biochemistry
• M.Pharmacy (Regulatory Affairs)

Key Responsibilities

• Prepare, review, and compile regulatory documents and dossiers.
• Coordinate with R&D, QA, QC, and Production teams.
• Maintain regulatory databases and documentation records.
• Ensure compliance with regulatory guidelines and company standards.
• Review labeling, packaging, and artwork for regulatory compliance.

Required Skills

• Basic knowledge of pharmaceutical regulatory requirements.
• Good communication and documentation skills.
• Attention to detail and analytical thinking.
• Ability to work effectively in a team.
• Proficiency in MS Office tools.

Last Date : 30th October 2026