Shilpa Biologics Hiring for Regulatory Affairs, Production, R&D, QC Microbiology
Shilpa Biologics, a subsidiary of Shilpa Medicare Ltd, is expanding its team and is currently hiring for key roles in Regulatory Affairs, Production, R&D, and QC Microbiology. Located in Dharwad, Karnataka, Shilpa Biologics offers state-of-the-art facilities and a dynamic environment for professionals looking to make an impact in the world of biologics.
With over 35 years of expertise in the formulations and API (Active Pharmaceutical Ingredients) industry, Shilpa Biologics is at the forefront of biopharma innovation, specializing in curative therapies and cutting-edge research.
Available Positions at Shilpa Biologics
Shilpa Biologics is seeking experienced professionals for multiple departments:
- Regulatory Affairs
- Experience Required: 3-5 years in biologics.
- Key Role: Ensuring regulatory compliance and liaising with health authorities to support product approval and manufacturing processes.
- Production (USP and DSP)
- Experience Required: 2-10 years.
- Key Responsibilities: Manufacturing processes, both Mammalian and Microbial production, and downstream processing (DSP).
- R&D (Research and Development)
- Experience Required: 1-8 years.
- Positions Available: Cell line development, bioassay, formulations, and analytical research.
- Key Role: Developing innovative biologics and supporting therapeutic advancements.
- QC Microbiology
- Experience Required: 2-5 years.
- Key Responsibilities: Quality control processes, microbial testing, and ensuring product safety and efficacy.
Each of these roles plays a crucial part in Shilpa Biologics’ mission to develop life-saving therapies, with a focus on curative treatments that address unmet medical needs.
How to Apply
Candidates with relevant experience in biologics are encouraged to apply for the above positions. Please submit your CV to harikrishnau@shilpabio.com