Advisor, Analytical CMC

Reposted Yesterday
Be an Early Applicant
Boston, MA, USA
In-Office
138K-224K Annually
Mid level
Healthtech • Biotech • Pharmaceutical
The Role
Develop, optimize, and validate analytical methods for gRNA, mRNA, and LNP products; coordinate method transfer with QC/CMOs; interpret and present data; author technical documents; provide technical oversight, troubleshoot assays, and mentor junior staff while collaborating cross-functionally.
Summary Generated by Built In

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.

Position Summary:

The Analytical Development group is responsible for developing and implementing new analytical methods, as well as optimizing and improving current methods for the characterization of raw materials, RNA drug substances, and LNP products and programs at various development stages.

Additionally, the role includes testing non-GMP samples to support development studies such as comparability assessments, process development, stability, product, and process characterization. The position is part of a Technical Operations team that partners closely with Quality Control, Quality Assurance, Process Development, and Analytical Research & Development.

Responsibilities:

  • Develop, optimize, and execute analytical methods intended for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials.

  • Review, interpret, and present data within the analytical team and cross-functional.

  • Provide technical oversight for troubleshooting and phase-appropriate qualification and validation of analytical assays for the analysis of gRNA, mRNA, and LNP. Work in partnership with internal and/or external QC to coordinate analytical method transfer within the organization or at Contract Manufacturing Organizations (CMOs)/Contract Testing Laboratories (CTLs).

  • Author, review, and revise technical source documents to support phase-appropriate comparability.

  • Serve as the CMC representative on cross-functional project teams.

  • Provide technical oversight to guide analytical/QC investigations, as needed.

  • Actively collaborate with internal and external process development and quality teams.

  • Train and mentor junior team members.

 

Basic Requirements:

  • PhD in Analytical Chemistry, Biochemistry, Biophysics or related disciplines with 3+ years experience in the Pharmaceutical or Biotech industry.

  • 3+ years of experience in LC and CE required

  • Strong technical background in assay development, validation and implementation to support target candidate validation from Analytical Development to Internal/external QC environments required

 

Additional Skills/Preferences:

  • Will also consider: MS degree with 7+ years of experience OR BS degree with 10+ years of Biotech industry experience.

  • Strong hands-on experience using multi-modal HPLC/UPLC LC-fluor, LC-MS, SEC-MALS, spectroscopic (UV/Vis, FTIR), capillary electrophoresis (CE).

  • Knowledge of advanced characterization instrumentation such as cryo-TEM, NMR, FFF-MALS, DLS, NTA, AUC etc.

  • Working experience developing methods for gRNA, mRNA, and LNPs is a plus.

  • Excellent scientific knowledge in analytical chemistry with a conceptual understanding of solid-phase oligonucleotide synthesis and purification strategies.

  • Familiarity with applicable ICH regulations and multi-compendial guidelines related to method validation.

  • Effective oral and written communication skills.

  • Advanced understanding of lipid nanoparticle delivery, production, and purification.

  • Proactive, creative, and positive attitude.

  • Demonstrated scientific and people leadership skills.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$138,000 - $224,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

Top Skills

Auc
Capillary Electrophoresis
Ce
Cryo-Tem
Dls
Fff-Mals
Ftir
Hplc
Lc
Lc-Fluor
Lc-Ms
Nmr
Nta
Sec-Mals
Uplc
Uv/Vis
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The Company
HQ: Indianapolis, IN
39,451 Employees
Year Founded: 1876

What We Do

Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment. For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.

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