Research Jobs at Baxter | MSc/MPharm Graduates Apply Now for the Associate Scientist Role
Baxter is seeking an Associate Scientist I (R&D – F&D) to join our Ahmedabad, Gujarat team. In this role, you will contribute to the formulation and development of injectable drug products, supporting both new product innovations and enhancements to existing therapies. As part of a mission-driven organization focused on saving and sustaining lives, you’ll collaborate with global cross-functional teams, drive projects using a Quality by Design (QbD) approach, and ensure compliance with international regulatory standards. This is an opportunity to make a meaningful impact while advancing your career in a purpose-led environment.
- Job Posting: Associate Scientist I – R&D
- Location: Ahmedabad, Gujarat, India
- Req ID: JR-177870
About the Company
Baxter is a global healthcare leader dedicated to saving and sustaining lives through innovative medical products and therapies. With a legacy spanning over 90 years, Baxter provides essential solutions in critical care, nutrition, renal, hospital, and surgical care across more than 100 countries. The company’s mission-driven culture focuses on advancing patient safety, delivering high-quality products, and driving innovation to meet evolving healthcare needs worldwide
Role Overview
As an Associate Scientist I in our R&D Formulation & Development (F&D) team, you will lead and support injectable drug product development, technology transfer, and regulatory submissions. This role involves hands-on formulation work, cross-functional collaboration, and ensuring compliance with global quality and regulatory standards.
Key Responsibilities
- Design and execute formulation and stability studies under a Quality by Design (QbD) framework.
- Compile and analyze development and stability data; prepare MFR, PDR, PDLM, protocols, and reports.
- Support process validation, technology transfer, and regulatory submissions.
- Troubleshoot during exhibit/commercial batches; handle OOS/OOT investigations.
- Collaborate with internal teams (Analytical, Regulatory, Manufacturing) and external partners (CMOs/CROs).
- Ensure cGxP compliance, documentation, equipment readiness, and safety (HIRA/EHS).
- Assist in regulatory responses, audits, and market complaint investigations.
- Identify and implement process improvements and new technologies.
What You’ll Need
- M.S. (Pharm.), M. Pharm., or Ph.D. in Pharmaceutics.
- 1–8 years’ experience in injectable formulation development and technology transfer.
- Strong technical writing, data analysis, and presentation skills.
- Knowledge of ICH, cGxP, and global regulatory guidelines (US FDA, EMA, MHRA).
- Experience in cross-functional and global team environments; project leadership a plus.
- Quality- and safety-focused mindset with ability to manage ambiguity and tight timelines.
Why Join Baxter?
- Opportunity to work on innovative healthcare solutions that improve lives worldwide.
- Collaborative culture with personal ownership and growth opportunities.
- Inclusive workplace that values diversity, equity, and work–life balance.
Baxter is an Equal Opportunity Employer.
We provide reasonable accommodations to qualified individuals with disabilities. Beware of recruitment scams; for details, see Baxter’s Recruitment Fraud Notice.
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