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Hiring Research Scientist in Bioproduct Analytical Development at Lilly

 

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Hiring Research Scientist in Bioproduct Analytical Development at Lilly

At Lilly, we make a difference for people the world over by discovering, developing and delivering the breakthrough medicines that help them live longer, healthier more active lives. What’s more, you can also count on us and our people to be incredibly civic-minded, supporting our communities through philanthropy, volunteerism and a creative and innovative can-do spirit.

Post : Research Scientist

Job Description
Main Purpose and Objectives of Position
As part of a multi-disciplinary team in BRD Analytical, a successful candidate would be an individual contributor on multiple project teams.  Responsibilities would include performing activities supporting an integrated analytical control strategy for a variety of active pharmaceutical ingredients, dosage forms, reference materials, and placebos.  Included in these responsibilities would be oversight of analytical methods from development to validation, identifying solutions to complex technical issues, and comprehensive documentation to advance the portfolio.

Key Responsibilities
• Understands and complies with corporate, divisional, and departmental procedures, including GMP, safety, and other regulations.
• Efficiently and effectively manage aspects of analytical control strategies of active pharmaceutical ingredients and drug products, as well as reference materials and placebos, for multiple projects in various phases of development.
• Demonstrates comprehensive knowledge of various techniques to enable troubleshooting and problem solving (e.g., HPLC, CE, ELISA, qPCR, Bioassay, Karl Fischer, UV, compendial and parenteral tests such as particulates).
• Oversight of development and verification / qualification / validation of methods to support in-process, release, characterization, and stability testing of active pharmaceutical ingredient and drug product.
• Openly shares technical knowledge and key learning while establishing relationships with key business partners.
• Ability to be flexible within the workday and effective at various forms of communication to enable participation in global team interactions.
• Effectively guide and oversee external work at collaboration partners.
• Demonstrates proficiency at data reporting, interpretation, and trending (e.g., Empower chromatography software and electronic laboratory notebooks).
• Demonstrates good documentation skills with regard to raw data recording and authoring of technical documents (e.g., technical reports, data integrity reviews, and submission components).
• Maintains awareness of analytical science advances, as well as pharmaceutical industry and regulatory trends.


Candidate Profile
•  P4 - BS / MS in analytical or related field with relevant pharmaceutical experience; alternatively, skills commensurate with a BS/MS chemist.
•  R1 / R2 – Ph.D. in analytical, or related field; alternatively, skills commensurate with a Ph.D. chemist.

Experience
• Previous pharmaceutical industry experience (preferably 5+ years) required.
• Chemistry experience with knowledge of one or more of the following, as appropriate: separation sciences, biophysical/ biochemical characterization, and bioanalytical sciences.
• Experience in large molecules and analytical development recommended.
• Capable of designing experiments and interpreting results independently.
• Ability to troubleshoot problems and identify solutions.
• Effective oral and written communication skills, self-management, task planning, and organization.
• Excellent general computer skills (MS Excel, Internet Explorer, PowerPoint, MS-Word, JMP) and the ability to compile, summarize, and present information to diverse groups.
• Must be able to work productively in an interdisciplinary team environment as well as to influence and partner with individuals outside of a formal reporting relationship towards realization of team goals.
• Experience with the drug development process, including knowledge of regulatory compliance issues.
• Fundamental knowledge of cGMP/GLP compliance requirements.
• Customer-focused attitude


Additional Information
Experience : 5+ years
Qualification :  M.Sc, M.Pharma
Location : Bangalore, Karnataka
Industry Type : Pharma / Healthcare / Clinical research
End Date : 10th February, 2023

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