Sun Pharmaceutical Industries Ltd, one of India’s most prestigious pharmaceutical giants, is inviting applications for a role in its cutting-edge Biotechnology Research & Development division in Tandalja. The position of Executive – SPR Method Development offers an exciting opportunity to work on biosimilars, therapeutic proteins, and innovative biotech solutions.
If you’re a life sciences graduate with 1–3 years of experience, strong lab skills, and a passion for analytical development, this might just be the role that defines your career.
🌞 About Sun Pharmaceutical Industries Ltd
Sun Pharma is the 4th-largest specialty generic pharmaceutical company globally, with a presence in over 100 countries. Its commitment to R&D, innovation, and affordable healthcare solutions has made it a household name in India and a recognized force worldwide.
Focusing on complex generics, biosimilars, and biologics, Sun Pharma is expanding its biotech footprint rapidly—and this opening is a part of that growth.
🧬 Job Role: Executive – Biotechnology (SPR Method Development)
🏢 Location: Tandalja (Sun Pharma R&D Center)
👨🔬 Experience: 1–3 Years
🎓 Qualification: M.Sc. in Biochemistry, Biotechnology, Life Sciences, or similar field
🔬 Department: R&D – Analytical Development (Biologics)
In this role, you’ll be working on Surface Plasmon Resonance (SPR) technology to study biomolecular interactions—an essential part of the biosimilar drug development process.
🔍 Key Responsibilities
As an Executive in Biotechnology at Sun Pharma, your focus will be developing and qualifying SPR-based methods and ensuring analytical consistency in biosimilar programs. Below are the core responsibilities you’ll manage:
1. SPR-Based Method Development
- Design and develop analytical protocols using SPR to assess binding constants (kinetic & equilibrium).
- Work with monoclonal antibodies and peptide-based products.
2. Analytical Similarity Studies
- Conduct similarity studies between in-house biosimilars and originator biologics sourced globally.
- Ensure that analytical results align with regulatory and efficacy benchmarks.
3. Characterization & QTPP Creation
- Characterize innovator biologics and build Quality Target Product Profiles (QTPP) for development goals.
4. Documentation & Compliance
- Draft Method Development Reports (MDR) and Analytical Test Procedures (ATP).
- Ensure adherence to Good Laboratory Practices (GLP) at every stage.
5. Instrument Management
- Operate and maintain SPR instruments with accuracy.
- Handle calibration and resolve equipment-related issues quickly.
6. Inventory & Reagent Handling
- Manage stocks of chemicals, consumables, and critical reagents used in method development.
🧠 Skills and Technical Expertise
This role demands both strong academic knowledge and hands-on lab skills. Here’s what Sun Pharma expects:
- ✔ Proficiency in SPR (Surface Plasmon Resonance) applications.
- ✔ Experience in biosimilarity testing and comparative studies (preferred).
- ✔ Hands-on exposure to monoclonal antibodies, peptides, and biologic drug formats.
- ✔ Working knowledge of analytical tools like HPLC, CE (Capillary Electrophoresis), and other biophysical techniques.
- ✔ Strong documentation and report-writing skills.
- ✔ Awareness of GLP, quality guidelines, and international biosimilar standards.
🧭 Career Growth & Why This Role Is a Game Changer
This is more than just a technical position—it’s a launchpad into advanced biotech R&D. Here’s why this opportunity stands out:
🌍 Exposure to Global-Grade Projects
Work on real-world biosimilar comparisons involving global-originator biologics, meeting global regulatory standards.
🧪 Deep Dive into Biologics
Get hands-on training in working with proteins, antibodies, and peptides—skills that are in high demand across biotech companies globally.
📈 Structured R&D Environment
Sun Pharma offers a rich ecosystem of mentorship, documentation systems, and compliance protocols, perfect for professional growth.
🧬 Entry to High-Value Domains
This job opens doors to career paths in:
- Biologic Analytical Development
- Regulatory Affairs (Biotech)
- Quality Control for Biopharmaceuticals
- Formulation Development (mAbs, Peptides)
👨💼 Who Should Apply?
This role is ideal for:
✅ Postgraduates (M.Sc.) in Biotechnology, Biochemistry, or Life Sciences
✅ Professionals with 1–3 years’ experience in analytical method development
✅ Scientists with a passion for biosimilar development & protein analytics
✅ Researchers interested in building a long-term career in regulated markets (EU, US, etc.)
🛡️ Perks & Benefits
- 🕓 Balanced Work-Life Culture
- 🧠 Challenging Research Projects in evolving therapeutic areas
- 🛡️ Insurance and Employee Support
- 📊 Exposure to Regulatory Submissions & International Standards
💬 Final Words
In today’s competitive biotech space, biological method development skills—especially around techniques like SPR—are becoming must-haves. Joining Sun Pharma’s R&D team at this level allows you to work with a globally recognized pharma leader while advancing your expertise in one of the most specialized domains of pharmaceutical research.
Whether you’re transitioning from academic research or looking for deeper industry exposure, this job role helps bridge that gap and grow your biotech career at the cutting edge.
Content Writer
