Cadila Pharmaceuticals
At Cadila Pharmaceuticals, innovation is more than a goal — it’s a commitment to advancing healthcare through cutting-edge pharmaceutical development. We’re excited to announce new opportunities in our Formulation & Development (F&D) division for Research Associate / Senior Research Associate – Formulation Development (Injectables) at our state-of-the-art facility in Dholka, Ahmedabad.
Why This Role Matters
Injectable formulations remain one of the most challenging and rewarding areas of pharmaceutical R&D. From aseptic processing to lyophilized and emulsion-based injectables, the work done in this department plays a pivotal role in delivering safe, effective, and life-saving medicines to patients around the world.
As part of our team, you’ll contribute to the design and development of formulations for global markets — including the US, EU, and ROW (Rest of the World) — ensuring they meet stringent regulatory standards and deliver consistent quality.
🔬 We’re Hiring: Research Associate / Senior Research Associate – Formulation Development (Injectables)
📍 Location: Dholka, Ahmedabad
🧪 Experience: 3–6 Years
🎓 Qualification: M.Pharm
🏢 Department: F&D (Injectables)
Are you passionate about injectable formulation development and looking for an opportunity to work on cutting-edge pharmaceutical projects?
We’re seeking highly motivated and detail-oriented professionals to join our growing F&D team!
🔑 Key Responsibilities:
• Prepare BOMs for new UID activities aligned with NPD costings
• Develop and deliver assigned formulations/projects on time and within budget
• Complete documentation to support pre-clinical, clinical, tech transfer, and exhibit batch activities
• Create non-infringing, regulatory-compliant formulation strategies for US, EU, and ROW
• Maintain accurate lab notebooks, compile stability data, and track project milestones
• Prepare and request specifications for raw materials, packaging, IPC, and finished products
• Draft/review documents like MFCs, PDRs, TT dockets, and ensure timely cross-functional coordination
• Identify product/process-specific equipment and maintain usage/maintenance records
• Ensure SOP, GLP, and GDP compliance throughout the development process.
🔎 Desired Candidate Profile:
✅ Hands-on experience with aseptic processing, lyophilized formulations, and suspension/emulsion injectables is a strong advantage.
✅ Strong understanding of regulatory expectations (USFDA, EMA, WHO, etc.).
Proficient in data analysis, scientific documentation, and technical report writing.
✅ Excellent team collaboration and cross-functional coordination skills.
👩🔬 If you have a strong background in injectables, a keen eye for quality, and a proactive approach to R&D—we want to hear from you!
📩 Apply now [[email protected]]
🌟 Be Part of a Culture of Excellence
At Cadila Pharmaceuticals, you’ll work alongside some of the brightest minds in the industry, with access to cutting-edge technologies and a collaborative environment that fosters continuous learning and growth.
If you are passionate about pharmaceutical R&D and ready to make a real impact in healthcare, this is your opportunity to grow with us.
📩 Apply Today!
Send your updated resume to [email protected]
📌 Subject Line: Application for RA/SRA – F&D (Injectables)
Together, let’s shape the future of healthcare—one formulation at a time.
To apply for this job email your details to drashti.chaudhari@cadilapharma.com.
