Lilly Research Scientist Job Opening 2021 – Apply Online
Lilly Research Scientist in Analytical Development Chemistry job opening at Lilly. Chemistry job opening at Lilly. Pharma job opening at Lilly. Lilly Research Scientist in Analytical Development Recruitment – Applications Invited. Research Scientist in Analytical Development Job Opening. Chemistry Scientist vacancy 2021.
Job Title: Research Scientist in Analytical Development
Location India, Bengaluru
Main Purpose and Objectives of Position
As part of a multi-disciplinary team in BRD Analytical, responsible to define the use of analytical control strategies and the use of analytical, bioanalytical, and characterization methods to design an integrated control strategy enabling process and product development. Responsible for developing the portfolio strategy and for the development and application of technical capabilities to the portfolio of synthetic small molecules, peptides, and oligonucleotides.
Key Responsibilities
- Understands and complies with corporate, divisional, and departmental procedures, including GMP, safety, and other regulations.
- Demonstrates technical excellence at performing and assessing multiple analytical methods to enable oversight of third-party labs. Displays comprehensive knowledge of various techniques to enable troubleshooting and problem solving (e.g., HPLC, GC, X-ray diffraction, Karl Fischer, UV, MS, Dissolution, Disintegration, compendial and parenteral tests – particulates).
- Develop all or portions of analytical control strategies including reference materials.
Oversight of the development and verification/qualification/validation of methods to support in-process, release, characterization analysis, and stability testing of active pharmaceutical ingredients and drug products. - Responsible for the introduction of new methodologies for optimization of existing modalities or development of control strategies for new modalities.
- Openly shares technical knowledge and key learning.
- Establishes relationships with key business partners.
- Workday flexibility 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 and regulatory documents (e.g., technical reports, data integrity reviews, and submission components).
- Maintain awareness of the external environment (industry and regulatory).
Eligibility Criteria:
Ph.D. in analytical, or related field; alternatively, BS/MS with skills commensurate with a Ph.D. chemist.
Experience Requirements
- 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 synthetic small molecule, peptide, and/or oligonucleotide process and analytical development recommended.
- Capable of designing experiments and interpreting results independently.
Problem solving and decision-making. - Effective oral and written communication skills, self-management, task planning and organization.
- Must be able to work productively in an interdisciplinary team environment.
Experience with the drug development process, including knowledge of regulatory compliance issues. - Fundamental knowledge of cGMP/GLP compliance requirements.
- License/Certificate Requirements
Language Requirements English
Travel Requirements 0-15% is typical
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