Apply now for RS Method Development role at Aurobindo Pharma in Bachupally, Hyderabad. Join our R&D team and shape the future of pharmaceutical innovation!

📢 We’re Hiring: RS Method Development Role at Aurobindo Pharma – Bachupally, Hyderabad

Aurobindo Pharma, a leading name in the global pharmaceutical industry, is expanding its R&D capabilities and inviting passionate professionals to join our RS Method Development team at our Bachupally facility in Hyderabad. If you are looking to elevate your career with an organization that values innovation, quality, and scientific excellence, this is the opportunity you’ve been waiting for.

🔬 About the Role – RS Method Development

The RS (Related Substances) Method Development role is a crucial part of our Research and Development (R&D) function. In this position, you will be at the forefront of analytical method development and validation for identifying related substances and impurities in pharmaceutical products. Your expertise will help ensure the safety, efficacy, and regulatory compliance of our drug formulations.

We are seeking experienced and dedicated professionals with a keen interest in analytical chemistry, method development, and chromatographic techniques to be a part of this mission-critical department.

✅ Job Details:

• Position: RS Method Development – R&D Department

• Location: Bachupally, Hyderabad

• Company: Aurobindo Pharma

• Department: Research & Development (Analytical)

• Type: Full-time

• Experience Required: 2–6 years preferred in RS method development or similar analytical R&D roles

• Email to Apply/Refer: sreeja.yangam@aurobindo.com

🧪 Key Responsibilities:

As a member of the RS Method Development team, your responsibilities will include:

• Designing, developing, and validating analytical methods for the identification and quantification of related substances and impurities in drug substances and drug products.

• Utilizing advanced instrumentation such as HPLC, UPLC, GC, LC-MS/MS, and FTIR for impurity profiling and method development.

• Conducting forced degradation and stability studies as per ICH guidelines.

• Supporting regulatory submissions by preparing analytical reports and method validation documentation.

• Collaborating with cross-functional teams including formulation, QA/QC, and regulatory affairs to ensure method robustness and reproducibility.

• Keeping up to date with the latest regulatory guidelines (e.g., ICH Q2, USP, EP, FDA).

• Troubleshooting analytical issues and optimizing chromatographic conditions for better separation of impurities.

🧑‍🔬 Preferred Candidate Profile:

To succeed in this role, the ideal candidate should meet the following criteria:

• Educational Qualification: M.Sc. in Analytical Chemistry / Organic Chemistry / Pharmaceutical Chemistry or M. Pharmacy (Pharmaceutics/Pharmaceutical Analysis).

• Experience: 2–6 years in RS Method Development / Analytical R&D in a regulated pharmaceutical environment.

• Strong working knowledge of HPLC, GC, UPLC, LC-MS, and method development techniques.

• Experience in ICH guidelines, method validation protocols, and analytical troubleshooting.

• Prior exposure to regulatory audits (USFDA, MHRA, TGA) is a plus.

• Good documentation practices and data integrity standards (ALCOA+ principles).

• Excellent communication and team collaboration skills.

🌟 Why Join Aurobindo Pharma?

At Aurobindo, we don’t just manufacture medicines—we shape the future of healthcare. By joining our R&D team, you’ll be working with some of the brightest scientific minds in the industry on projects that change lives.

Here’s what makes Aurobindo a great place to work:

✔ Innovation-Driven Culture

We invest heavily in R&D and value original thinking. You’ll get opportunities to experiment, explore, and create.

✔ Career Growth Opportunities

We offer a structured career path with performance-based growth and learning opportunities through ongoing training and skill enhancement.

✔ World-Class Infrastructure

Our Bachupally R&D center is equipped with cutting-edge analytical instrumentation and technologies.

✔ Competitive Compensation

We offer industry-standard remuneration and a comprehensive benefits package, including health insurance, provident fund, performance bonuses, and more.

✔ Global Presence

Work on projects that cater to regulatory markets like the US, EU, and emerging economies.

📍 Location Advantage: Bachupally, Hyderabad

Our R&D facility is situated in Bachupally, one of Hyderabad’s fastest-growing pharma and biotech hubs. The area offers:

• Easy connectivity to major parts of Hyderabad

• Affordable housing and good quality of life

• Presence of multiple educational institutions and residential communities

📩 How to Apply

Ready to take the next step in your pharmaceutical career?

✅ Apply Now or Refer a Friend!

📧 Send your updated CV to: sreeja.yangam@aurobindo.com

Ensure to include the subject line: Application for RS Method Development – Bachupally

🔄 Refer & Earn!

Even if you’re not looking for a change, you can refer a friend or colleague who fits this role. Help someone else grow while being part of our employee referral program.

📝 Pro Tips Before You Apply:

• Highlight your RS method development and HPLC/UPLC experience in your resume.

• Include details of any regulatory audits you’ve been part of.

• Mention instruments and analytical techniques you are proficient in.

• If you’ve worked on method validation reports or stability studies, make sure that’s clearly listed.

🚀 Join Us and Make a Difference

This is more than just a job—it’s your chance to be a part of pharmaceutical breakthroughs that impact global health. Join Aurobindo Pharma and contribute to the science of tomorrow.

👉 Apply today and accelerate your career with one of India’s top pharmaceutical companies!