REMOTEFULLTIME
Advisor / Sr Advisor - Synthetic Molecule Analytical Chemistry
Eli Lilly and Company
Remote · remote · Posted 13d ago
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Undisclosed5–10 yrsfulltimeRemote
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Section · 01
About this role
Job Summary
Role Overview and Key Responsibilities
Scientific Technical Leadership
People Leadership
Basic Qualifications
Additional Skills/Preferences
Additional Information
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
PRD / SMDD Bangalore has an exciting opportunity for an Advisor / Sr Advisor - Synthetic Molecule Analytical Chemistry to join our multidisciplinary team of chemists and engineers. The individual will have technical oversight of key process development activities performed at a strategic Indian contract development and manufacturing organization (CDMO). The individual will act as the technical bridge between Lilly scientists and the CDMO, review influence CDMO strategies, ensure alignment with Lilly requirements, escalate risks and develop mitigation plans.
Empowered by access to world-class capabilities and extensive pharmaceutical development experience, you will help deliver technical solutions that enable deeper understanding of processes and products across the portfolio. Ideal candidates will possess experience across multiple analytical techniques ( e.g. , HPLC, mass spectrometry, NMR), demonstrate an aptitude in technical problem-solving, and be motivated to work both independently and collaboratively in a dynamic environment. The individual will enable comprehensive characterization of materials and processes necessary to ensure the quality, safety, and efficacy of Lilly's medicines. This responsibility requires direct contribution to the development of analytical methodology and the design of experiments to generate key data.
This position is in Hyderabad
Role Overview and Key Responsibilities
Scientific Technical Leadership
- Demonstrate learning agility across modalities (small molecules, peptides, and oligonucleotides). Drive the design, development, and implementation of product control strategies for synthetic / small molecule programs. Demonstrated ability to develop analytical methods, justify specifications, design stability studies, establish starting material rationales for synthetic processes, identify impurities, and test drug product performance characteristics ( e.g. , dissolution/disintegration).
- Provide technical guidance for analytical activities carried out within the CDMO network. Ensure methods are technically sound, well developed, and fit for purposes. Collaborate closely with process development chemistry and engineering colleagues and manufacturing engineers to translate processes from the bench to pilot plant scale.
- Identify and implement innovative solutions to development challenges, monitor emerging trends in analytical chemistry, and maintain familiarity with applicable regulatory requirements.
- Proven record of embracing advanced digitization efforts by deploying digital tools to enable seamless digital technology transfer.
- Proven track record of working with diverse groups across the value chain and in multiple locations.
- Thrive at the interface between disciplines and be able to quickly move from one scientific challenge to another while navigating ambiguity.
- Document all work in an appropriate manner.
People Leadership
- Exhibit coaching and mentoring of peers and other scientists.
- Work as a team and take responsibility with accountability.
- Promote a team culture of scientific excellence, collaboration, safety, and compliance.
Basic Qualifications
- PhD in Analytical Chemistry, Biochemistry, Chemistry, or related field, with 5+ years of experience
Additional Skills/Preferences
- Use of strong interpersonal skills for collaboration
- Demonstrated self-initiative and appropriate risk-taking
- Ability to learn and apply technical knowledge to meet changing project needs
- Ability to prioritize multiple activities and handle ambiguity
Additional Information
- Potential exposure to chemicals, allergens, and loud noises
- Work hours flexibility to accommodate collaboration across multiple time zones
- Travel: up to 20%. Mainly domestic. Occasionally international.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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Section · 02
Skills
Pilot PlantPeptidesProduct researchChemistryMass spectrometryProduct controldigital technologycharacterizationprocess developmentHPLCBiochemistrydesign of experimentsChemicalsManufacturingcompliancePharmaceutical
Section · Company
About Eli Lilly and Company
Eli Lilly and Company
Pharma
2.7k+
employees
1993
33 years old
Indianapolis, Indiana
United States (USA)
₹23.4L PA avg
Avg at Eli Lilly and Company
About
Lilly unites caring with discovery to create medicines that make life better for people around the world.
Industries
Pharma
Employee ratings
10 reviews
3.7/ 5
Culture
2.2
Career growth
2.0
Work-life
3.3
Employees rate it well for
Work-Life Balance39Job Security38
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