Director, External Quality Control & Stability

Eli Lilly and Company

Indianapolis (IN)

Remote

USD 117,000 - 260,000

Full time

29 hours ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Centessa Pharmaceuticals, a wholly owned Lilly subsidiary, seeks a Director of External Quality Control & Stability to lead analytical QC strategy across multiple programs and oversee stability design and regulatory compliance.

This remote US-based role requires 10+ years in QC and analytical development, with a proven ability to drive strategic vision and coordinate method validation, transfer, supplier oversight, and regulatory submissions.

Qualifications

  • BS/MS/PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
  • 10+ years quality control and analytical development experience.
  • Experience developing strategic vision as well as providing tactical support for quality control programs

Responsibilities

  • Analytical Oversight and Tactical Support: Develop and lead analytical quality control strategy across multiple programs.
  • Review analytical methods, specifications, and validation activities for adequacy and collaborate on updates.
  • Support analytical method transfer, as required.
  • Collaborate on supplier qualification and/or remediation activities.
  • Stability Program Leadership: Oversee the stability program design and execution across multiple programs.
  • Monitor and report on stability trends and product quality attributes as required.
  • Ensure ongoing regulatory compliance of stability activities.
  • Supplier Oversight: Manage supplier ongoing relationships.
  • Perform routine reviews of testing results and overall quality of documentation.
  • Drive issue resolution to facilitate regulatory compliance.
  • Regulatory Support: Provide tactical support for regulatory submissions.
  • Support health authority inspections and audits, as required.
  • Review analytical and stability sections within CMC filings.

Skills

Analytical development
Quality control
Strategic vision

Education

BS/MS/PhD in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

Analytical methods
Stability testing

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Overview

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions. Headquartered in Boston, Massachusetts, Centessa was recognized as a Great Place to Work® in 2026.

The Director, External Quality Control & Stability will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development.

Responsibilities
Analytical Oversight and Tactical Support
  • Develop and Lead analytical quality control strategy across multiple programs.
  • Review analytical methods, specifications, and validation activities for adequacy and collaborate on updates, as required.
  • Support analytical method transfer, as required
  • Collaborate on supplier qualification and/or remediation activities.
Stability Program Leadership
  • Oversee the stability program design and execution across multiple programs.
  • Monitor and report on stability trends and product quality attributes as required.
  • Ensure ongoing regulatory compliance of stability activities.
Supplier Oversight
  • Manage supplier ongoing relationships.
  • Perform routine reviews of testing results and overall quality of documentation.
  • Drive issue resolution to facilitate regulatory compliance.
Regulatory Support
  • Provide tactical support for regulatory submissions
  • Support health authority inspections and audits, as required.
  • Review analytical and stability sections within CMC filings.
Basic Qualifications
  • BS/MS/PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
  • 10+ years quality control and analytical development experience.
  • Experience developing strategic vision as well as providing tactical support for quality control programs
Work Location

The Director, External Quality Control & Stability role is a remote role based in the US.

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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $117,000 - $259,600

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

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Director, External Quality Control & Stability
Director, External Quality Control & Stability

100 Eli Lilly and Company • United States

Remote
USD 117,000 - 260,000
Senior Director, Analytical Development CMC
Senior Director, Analytical Development CMC

Eli Lilly and Company • United States

Remote
USD 153,000 - 290,000
401(k) plan
Pension
Vacation benefits
+3
Associate Director, Product Quality
Associate Director, Product Quality

BioSpace • Indianapolis (IN)

On-site
USD 117,000 - 189,000
Company bonus
401(k) plan
Medical benefits
+4
Senior Advisor, Clinical Pharmacology
Senior Advisor, Clinical Pharmacology

Eli Lilly and Company • United States

Remote
USD 153,000 - 268,000
Performance bonus
401(k) plan with company match
Healthcare, dental, vision benefits
+1
Senior Director, Global Medical Affairs
Senior Director, Global Medical Affairs

Eli Lilly and Company • Indiana

Remote
USD 177,000 - 339,000
Bonus eligibility
401(k)
Pension
+5
Senior Director, Regulatory CMC (remote)
Senior Director, Regulatory CMC (remote)

Lilly • Boston (MA)

Remote
USD 176,000 - 284,000
401(k) matching
Pension
Health, dental, vision benefits
+1
Senior Director, Regulatory CMC (remote)
Senior Director, Regulatory CMC (remote)

Lilly • Indianapolis (IN)

Remote
USD 176,000 - 284,000
401(k)
Pension
Vacation benefits
+2
Senior Advisor, Clinical Pharmacology
Senior Advisor, Clinical Pharmacology

Eli Lilly and Company • Boston (MA)

On-site
USD 153,000 - 268,000
401(k) plan
Pension
Vacation benefits
+3
Senior Director, Drug Product CMC
Senior Director, Drug Product CMC

Eli Lilly and Company • Indiana

On-site
USD 164,000 - 264,000
Senior Advisor, Clinical Pharmacology
Senior Advisor, Clinical Pharmacology

BioSpace • Indianapolis (IN)

On-site
USD 153,000 - 268,000
Bonus program
Comprehensive benefits