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Advisor, Senior – Synthetic Molecule Analytical Chemistry
Eli Lilly and Company. Provide technical oversight of key process development activities at a strategic Indian CDMO .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Analytical Chemistry with a focus on developing and implementing analytical methods, ensuring compliance with regulatory requirements, and providing technical guidance across diverse teams. Proven ability to innovate and adapt strategies for process development in a CDMO environment.
Highest-signal resume keywords
PhD In Analytical ChemistryExperience With HPLCExperience With Mass SpectrometryExperience With NMRRegulatory Requirements Familiarity
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Analytical Method DevelopmentSpecification JustificationStability Study DesignStarting Material Rationale EstablishmentImpurity IdentificationDrug Product Performance TestingTechnical Guidance ProvisionDigital Technology Transfer DeploymentProcess Development CollaborationEmerging Trends Monitoring
Soft Skills
Strong Interpersonal SkillsSelf-InitiativeRisk-TakingFlexibilityCollaboration
Tools & Technologies
Digital Tools
Industry Keywords
CDMOSynthetic ProgramsSmall Molecule ProgramsAnalytical ChemistryScientific ExcellenceSafetyCompliance
About the role
Key responsibilities & impact- Provide technical oversight of key process development activities at a strategic Indian CDMO
- Act as the technical bridge between Lilly scientists and the CDMO
- Review and influence CDMO strategies
- Ensure alignment with Lilly requirements
- Escalate risks and develop mitigation plans
- Deliver technical solutions enabling deeper understanding of processes and products
- Design, develop, and implement product control strategies for synthetic and small molecule programs
- Develop analytical methods, justify specifications, design stability studies, establish starting material rationales, identify impurities, and test drug product performance characteristics
- Provide technical guidance for analytical activities across the CDMO network
- Collaborate with process development chemistry, engineering, and manufacturing engineering colleagues to translate processes from bench to pilot plant scale
- Identify and implement innovative solutions to development challenges
- Monitor emerging trends in analytical chemistry
- Deploy digital tools for seamless digital technology transfer
- Document all work appropriately
- Coach and mentor peers and other scientists
- Promote a culture of scientific excellence, collaboration, safety, and compliance
Requirements
What you’ll need- PhD in Analytical Chemistry, Biochemistry, Chemistry, or related field
- 5+ years of experience
- Experience with analytical techniques such as HPLC, mass spectrometry, and NMR
- Ability to develop analytical methods, justify specifications, design stability studies, establish starting material rationales, identify impurities, and test drug product performance characteristics
- Ability to provide technical guidance for analytical activities and ensure methods are technically sound and fit for purpose
- Familiarity with applicable regulatory requirements
- Experience deploying digital tools for digital technology transfer
- Track record of working with diverse groups across the value chain and multiple locations
- Strong interpersonal skills for collaboration
- Self-initiative and appropriate risk-taking
- Ability to learn and apply technical knowledge to changing project needs
- Ability to prioritize multiple activities and handle ambiguity
- Flexibility to accommodate collaboration across multiple time zones
- Willingness to travel up to 20%, mainly domestically and occasionally internationally
- Ability to work with potential exposure to chemicals, allergens, and loud noises
Benefits
Comp & perks- Opportunity to work on life-changing medicines and improve global health
- Work with world-class capabilities and extensive pharmaceutical development experience
- Collaboration with multidisciplinary, global teams
- Coaching and mentoring opportunities
- Work hours flexibility to accommodate collaboration across multiple time zones