Lilly Analytical Scientist Job Opening – Apply Online
Analytical Scientist
Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full Time Regular
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Organization Overview:
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana, USA. Our 39,000 employees worldwide work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.
The Product Research and Development (PRD) organization strives to develop and deliver quality medicines to patients. The portfolio consists of the development and commercialization of:
- Insulins
- Small molecules
- Monoclonal antibodies
- Novel therapeutic proteins
- Peptides
- Oligonucleotide therapies
- Gene therapy systems
This multidisciplinary group collaborates with therapeutic business units and manufacturing to deliver Lilly’s clinical portfolio to patients worldwide.
The Lilly Capability Centre India (LCCI) in Bengaluru is a strategic investment to attract top talent from India’s vibrant academic and professional environment. The LCCI group in India houses a PRD team that works closely with the PRD team in Indianapolis to enable the delivery of Lilly’s portfolio.
Responsibilities and Skillsets:
The individual will be part of a multi-disciplinary team in Synthetic Molecule Design and Development (SMDD) and Bioproduct Research and Development (BRD) Analytical organizations within PRD.
- Contribute to one or more project teams working on small or large molecules.
- Perform activities to evaluate the stability of active pharmaceutical ingredients (API) and dosage forms to support clinical trials and product development.
- Assist in activities like testing, evaluation, and release/disposition of raw materials and excipients.
- Develop and execute analytical methods for oral and/or parenteral products.
- Understand compendial method requirements and procedures for raw materials, drug substances, and drug products.
- Test and evaluate release and stability data, troubleshoot methods, and manage method development, qualification, validation, and transfer.
- Handle various analytical techniques, including:
- HPLC, GC, CE-SDS, SEC, ELISA, qPCR
- DSC, Bioassay, Karl Fischer, UV, LC-MS
- Dissolution, Disintegration, X-ray diffraction
- Work on analytical methods for:
- Antibodies/bifunctional/fusion proteins/proteins
- Peptides/oligonucleotides/other genetic medicines
- Small molecules/other synthetic molecules
- Raw materials and packaging materials testing
Other Key Responsibilities:
- Understand and adhere to business, compliance, regulatory (cGMPs), quality, environmental, and safety expectations.
- Proactively communicate with other scientists and management.
- Manage project deliverables with ownership and accountability.
- Develop and maintain strong professional relationships with internal and external stakeholders.
- Author regulatory documents and follow good documentation practices (e.g., Empower, NuGenesis, Signals (eLN)).
- Demonstrate proficiency in data integrity review, analysis, reporting, and trending.
- Author and track change controls.
- Conduct laboratory investigations and address OOT/OOS/aberrant data with root cause analysis and CAPA implementation.
- Support inspection readiness activities and internal/external audits.
- Utilize tools like Power BI, Python, and databases.
Educational Requirements:
- MS with 1–5 years of experience or BS with 3–5 years of experience in the analytical department of a pharmaceutical organization developing API or DP for clinical or commercial use.
Link to apply: APPLY ONLINE HERE
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