About Company:
Hetero is one of India’s leading generic pharmaceutical companies and the world’s largest producer of anti-retroviral drugs. Backed by 25 years of expertise in the pharmaceutical industry, Hetero’s strategic business areas spread across APIs, generics, biosimilars, custom pharmaceutical services and branded generics. The company is globally recognized for its strengths in Research and Development, manufacturing and commercialization of a wide range of products. Hetero has 36 state-of-the-art manufacturing facilities strategically located worldwide, approved by stringent global regulatory authorities. Our portfolio includes 300 plus products encompassing major therapeutic categories such as HIV/AIDS, Oncology, Cardiovascular, Neurology, Hepatitis, Nephrology, Urology, Diabetes, Ophthalmology, Hepatology and Immunology etc. Hetero has a strong global presence in over 145+ countries and focusses on making affordable medicines accessible to patients worldwide.
Website
http://www.hetero.com
Vacancy Details:
Job Description:
Exciting Opportunity at HETERO R&D!
We’re hiring passionate professionals to join our thriving R&D team and contribute to 30+ years of pharmaceutical excellence. If you have experience in HPLC Method Development, Calibration Review of Analytical Instruments, or HPLC Method Development using QbD, we’d love to meet you!
Walk-in Interview Details:
Date: 11th April 2025
Time: 10:00 am – 01:00 pm
Venue: Hetero R&D, Balanagar, Hyderabad, Telangana – 500018
Open Roles & Experience Required:
1.HPLC Method Development (3–7 years)
2.Calibration Review – Analytical Instruments (7+ years)
3.HPLC Method Development using QbD (10–12 years)
What to Bring:
1.Updated Resume
2.Last 3 Months’ Payslips
3.Passport-size Photograph
4.Experience Certificates
Be a part of shaping the future of healthcare with us!
Be part of a thriving organization with 30+ years of pharmaceutical excellence. Together, let’s shape the future of healthcare.
Requirements:
1.HPLC Method Development (3-7 Years)
1.Development of assay and related substances methods by HPLC for KSMs, intermediates, and drug substances
2.Experience in mini-validations and forced degradation (FD) studies
Il Calibration Review – Analytical Instruments (7+ Years)
1.Review calibration data for HPLC, GC, KF, Auto Titrator, Optical Rotation, etc.
2.Ensure compliance and data integrity
III.HPLC Method Development using QbD (10-12 Years)
1.Method development using QbD approach for assay & related substances
2.Skilled in QbD tools/software
3.Conduct validations & FD studies
4.Prepare/review validation protocols and QbD documentation
What to Bring:
1.Updated Resume
2.Last 3 Months’ Payslips
