Hetero, a leading global pharmaceutical company, is hiring Analytical R&D (OSD) Method Validation professionals for its Jadcherla facility. This is a golden opportunity for candidates with 1–4 years of experience in Method Validation to grow their careers with a top pharmaceutical player.
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If you have strong technical expertise and a passion for regulatory compliance, this role is tailor-made for you.
🔹 Key Responsibilities
- Perform method validation and transfer activities for oral solid dosage (OSD) forms.
- Develop, validate, and review analytical methods in line with ICH, USP, and regulatory guidelines.
- Support troubleshooting during validation and ensure accurate documentation.
- Collaborate with cross-functional teams for compliance with global regulatory standards.
- Maintain data integrity, audit readiness, and timely project delivery.
🔹 Required Qualifications
- Education: M.Pharm / M.Sc. in Analytical/Pharmaceutical Chemistry or related field.
- Experience: 1–4 years in Analytical R&D – Method Validation (OSD).
- Hands-on experience with HPLC, GC, Dissolution, and related analytical instruments.
- Sound knowledge of regulatory guidelines (ICH, USFDA, WHO, EMA, etc.).
- Strong documentation and reporting skills.
🔹 Benefits of Working at Hetero
- Competitive salary and benefits package.
- Exposure to global regulatory standards.
- Opportunity to work with cutting-edge technology in OSD development.
- Career growth in one of India’s leading pharmaceutical organizations.
📩 How to Apply
Interested candidates can share their updated CVs at:
Email: vijaybabu.r@hetero.com
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