Sun Pharma Careers: Manager Role in R&D | Apply Now
Are you looking for a Manager LC-MS Job at a leading pharmaceutical company? Sun Pharma Careers has announced a Manager Role in R&D for professionals interested in advancing their Chemistry Careers. This is an exciting opportunity that focuses on LC-MS method development, biologics characterization, regulatory documentation, and GLP-compliant laboratory operations.
About Sun Pharma
Sun Pharmaceutical Industries Ltd is one of India’s largest pharmaceutical companies and a leading global specialty generics organization. Headquartered in Mumbai, the company develops, manufactures, and markets high-quality pharmaceutical formulations and active pharmaceutical ingredients (APIs) across regulated and emerging markets. Sun Pharma is widely recognized for its strong R&D capabilities, advanced analytical laboratories, and global regulatory expertise. The company invests significantly in innovation, biologics research, complex generics, and specialty products. Through Sun Pharma Careers, professionals can explore rewarding Manager Role opportunities in pharmaceutical R&D, supporting advanced LC-MS method development, and expanding long-term Chemistry Careers in a globally respected organization.
- Job Title: MANAGER – 2
- Location: Tandalja – R&D
Key Responsibilities:
- The candidate is expected to develop LC-MS-based methods for protein and peptide product characterization.
- The candidate is expected to qualify the methods for the intended purpose for all pipeline products.
- The candidate is expected to design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product-related variants and impurities. Develop and apply novel sample preparation with emphasis on LC-MS, CEX-MS, and SEC-MS. Characterize innovator product batches sourced from different geographical regions and prepare a quality target profile.
- Responsible for designing advanced workflows such as multi-attribute methods for PTMs, sequence variants, qualitative and quantitative profiling of HCPs, Disulfide shuffling and bond analysis, cell culture metabolite analysis, glycan analysis, etc.
- Preparation and review of method development reports (MDR) and analytical test procedures (ATP).
- Responsible for operating and maintaining the analytical laboratory in compliance with GLP regulations.
- The candidate is responsible for the operation and maintenance of the MS instruments.
- To manage chemicals, consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshot instrument performance and equipment issues.
- Responsible for managing the regulatory queries.
- The candidate is expected to draft the technical content for the regulatory dossier.
