Advisor Process Analytical Technologies Lilly Medicine Foundry

Eli Lilly and Company

Hybrid

Quick summary

Work type: Hybrid
Location: IN
Salary: $126,000–$204,600 / yr
Posted: 3 days ago

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $177k

This role $165k

$115k most similar roles pay here $228k

This role pays less than 54% of similar roles. Most pay $137,562–$216,800 — the shaded band above. At the midpoint, this role pays about $165k versus about $177k for comparable roles.

Based on 238 similar postings.

Employer

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that discovers, develops, and markets medicines in areas such as diabetes, oncology, neuroscience, and immunology, known for products like insulin and Mounjaro. Industry: Pharmaceuticals

View all roles at Eli Lilly and Company

At a glance

TL;DR · Advisor Process Analytical Technologies Lilly Medicine Foundry

Apply Now Log in to save

Join Lilly as a Process Analytical Technology (PAT) Advisor at the newly established Lilly Medicine Foundry, a cutting-edge facility combining research and manufacturing. This technical-track position requires a collaborative PAT scientist to lead analytical strategies for drug substance production, ensuring compliance with GMP standards while fostering a safety-focused culture. You will drive the adoption of advanced automation tools like synTQ, mentor scientific staff, and collaborate across development and manufacturing teams to support clinical trials and regulatory submissions. Ideal candidates hold a Ph.D. in chemistry or chemical engineering, with expertise in pharmaceutical product development and cGMP compliance, along with experience in LC/MS and GC/MS technologies.

Skills

Python SQL LabVIEW R PAT LC/MS GC/MS cGMP SOPs synTQ GLP GMP Pharmaceutical Development Analytical Methods Validation Automation Development Technical Transfer Regulatory Submissions Project Management Quality Assurance Process Monitoring Continuous Improvement

What you'll do

Drive implementation of PAT strategies for drug substance production.
Investigate feasibility and ensure technical soundness of instruments for in-line monitoring.
Mentor scientific staff to ensure continuous professional growth and knowledge sharing.
Plan and manage development activities, including setting agendas and timelines.
Author or contribute to critical technical documents such as SOPs and regulatory submissions.

What we're looking for

Ph.D. in chemistry, chemical engineering, or related field; OR B.S./M.S. with 10+ years of experience.
Expertise leading analytical efforts in pharmaceutical product development and commercialization.
Strong knowledge of cGMP compliance requirements and practical cGMP experience.
Experience developing, validating, and transferring analytical methods to manufacturing operations.
Demonstrated ability to drive change and manage multiple activities under ambiguity.
Excellent communication, organizational, and leadership skills for team mentorship.