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Center For Breakthrough Medicines Jobs (NOW HIRING)

... breakthrough medicines - and make a direct impact on people's lives around the world! *This is a full-time onsite role located at ABEC's Wilson, NC facility* Company Background: For over 50 years ...

... breakthrough medicines - and make a direct impact on people's lives around the world! *This is a full-time onsite role located at ABEC's Wilson, NC facility* Company Background: For over 50 years ...

... breakthrough medicines - and make a direct impact on people's lives around the world! *This is a full-time onsite role located at ABEC's Wilson, NC facility* Company Background: For over 50 years ...

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Center For Breakthrough Medicines information

What are the key skills and qualifications needed to thrive at the Center for Breakthrough Medicines?

To succeed at the Center for Breakthrough Medicines, you typically need a background in life sciences or engineering, experience with bioprocessing or cell and gene therapy, and relevant advanced degrees or certifications. Familiarity with GMP regulations, laboratory automation systems, and quality management tools is often required. Strong problem-solving, teamwork, and communication skills are crucial for collaborating across multidisciplinary teams and ensuring operational excellence. These skills and qualifications are vital for driving innovation and maintaining regulatory compliance in a cutting-edge biomanufacturing environment.

What are common challenges faced by professionals at the Center for Breakthrough Medicines, and how can new team members prepare for them?

Professionals at the Center for Breakthrough Medicines often work in a fast-paced, rapidly evolving environment focused on advanced therapies and biomanufacturing. Common challenges include adapting to new technologies, managing tight project timelines, and ensuring strict regulatory compliance. New team members can prepare by staying up-to-date on industry best practices, being proactive in communication, and embracing a collaborative mindset to work effectively across multidisciplinary teams. Familiarity with cGMP standards and a willingness to learn are also key to overcoming these challenges and succeeding in this dynamic setting.

What is the Center for Breakthrough Medicines?

The Center for Breakthrough Medicines (CBM) is a contract development and manufacturing organization (CDMO) focused on cell and gene therapy. It provides manufacturing, process development, analytical testing, and support services to biopharmaceutical companies developing advanced therapies. CBM helps clients bring innovative treatments from the research phase through clinical trials and commercial production. Their state-of-the-art facilities and expertise aim to accelerate the development and delivery of life-changing medicines.

What is the difference between Center For Breakthrough Medicines vs Pharmaceutical Manufacturing Technician?

AspectCenter For Breakthrough MedicinesPharmaceutical Manufacturing Technician
Required CredentialsRelevant degrees in life sciences, GMP trainingHigh school diploma or equivalent, GMP certification often preferred
Work EnvironmentResearch labs, manufacturing facilities, collaborative teamsManufacturing floors, quality control labs, production lines
Employer & Industry UsageBiotech and pharmaceutical companies focusing on innovative therapiesPharmaceutical companies, contract manufacturing organizations
Common Search & Comparison IntentUnderstanding roles in biotech manufacturingJob responsibilities and qualifications in pharma production

Center For Breakthrough Medicines typically involves research and development in biotech settings, requiring specialized degrees and GMP training. Pharmaceutical Manufacturing Technicians focus on production processes within pharmaceutical manufacturing facilities, often with less formal education but GMP certification. Both roles are essential in the pharmaceutical industry but differ in responsibilities and work environments.

More about Center For Breakthrough Medicines jobs
What cities are hiring for Center For Breakthrough Medicines jobs? Cities with the most Center For Breakthrough Medicines job openings:
What states have the most Center For Breakthrough Medicines jobs? States with the most job openings for Center For Breakthrough Medicines jobs include:
Infographic showing various Center For Breakthrough Medicines job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution.

Director/Sr. Director/Exec. Director, Molecular Pharmacology (AMD)

Eli Lilly and Company

San Francisco, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

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: Molecular Pharmacology Lead in South San Francisco, CA

Reports to: Head of Molecular Pharmacology, Lilly Research Laboratories

Band: Strategic and Scientific Team Leader

Overview

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

The Lilly Small Molecule Design group is an organization purpose-built to create molecules that make life better for people. We focus on using cutting edge science to unlock new approaches that can treat people suffering from diseases with poor treatment options. We continually challenge ourselves to deliver molecules that can provide breakthrough efficacy with the highest possible safety margins. We are dedicated to optimizing our mindset, technology, and processes for faster, more nimble execution. Our success is built on a culture that empowers innovative problem solving through open collaboration and individual accountability.

Position Summary

The Advanced Molecule Design team's mission is to optimize lead molecules to strong drug candidates that become breakthrough medicines. Molecular Pharmacology People Managers (L2) are scientific leaders who drive team performance by combining deep pharmacology expertise with strong people leadership. These roles are responsible for building and sustaining highly effective teams that deliver high-quality data, advance drug discovery programs, and develop the next generation of scientists. L2 leaders are expected to excel in both scientific leadership and people development - delivering on functional goals while creating an environment where scientists thrive and grow.

Key Responsibilities

Technical / Scientific Contributions: Champion Rigorous Science and Deliver on Functional Goals

  • Establish robust screening cascades; lead the team to deliver highly reproducible, high-quality assays that drive SAR and compound optimization.

  • Routinely investigate and guide mechanistic characterization of molecules in vitro to inform compound optimization and target product profiles.

  • Make sound scientific decisions that advance programs while maintaining quality - balance speed with scientific rigor.

  • Focus the team on the highest-impact activities that advance programs toward patients.

  • Design screening cascades that enable clear, data-driven go/no-go decisions.

  • Act with speed and decisiveness on critical scientific issues; surface challenges early with radical transparency.

Enabling: Partnerships and Tools That Accelerate Impact

  • Lead cross-functional collaboration; partner with Medicinal Chemistry, Computational Chemistry, ADME, and other functions to advance program goals.

  • Directly mentor and guide scientists to embrace and implement AI, automation, and new technologies into workflows.

  • Build ONE TEAM, SAME TEAM collaboration - break down silos and foster partnerships that accelerate programs.

  • Build scientific credibility and influence across the organization through deep expertise and strategic thinking.

Supporting: People Leadership and Team Development

  • Elevate individual and team performance consistently - provide coaching, feedback, and development that increases impact.

  • Develop scientists across all four competency areas: Deep Thinking, Execution & Delivery, Culture & Teamwork, and Growth Mindset.

  • Cultivate a growth mindset within the team; address performance gaps and adherence to Lilly cultural standards promptly and constructively.

  • Make fair, evidence-based performance assessments; differentiate based on impact and consistency.

  • Have courageous conversations - celebrate excellence and address performance gaps directly and constructively.

  • Create conditions where scientists can be successful - remove barriers, provide resources, and empower the team.

  • Contribute to a work environment that fosters support, collaboration, professionalism, mutual respect, and patient focus.

  • Be accessible - make time for your team and create an environment where people feel comfortable bringing challenges forward.

Safety & Compliance - Model Safety Leadership Through Personal Practice

  • Demonstrate an unwavering commitment to safety-first laboratory practice: complete required safety training, conduct risk assessments before experiments, and escalate concerns immediately.

  • Follow all site safety, environmental, and regulatory compliance requirements; actively reinforce a safety-first team culture.

Basic Requirements

  • PhD Degree in Biochemistry, Biology, Biophysics, Molecular Biology, Pharmacology, or related fields with a minimum of 15+ years of drug discovery experience in the pharmaceutical industry; or BS/MS Degree in Biochemistry, Biology, Biophysics, Molecular Biology, Pharmacology, or related fields with 20+ years of equivalent experience.

Additional Preferences

  • Demonstrated drug discovery experience with a track record of delivering high-quality pharmacology data that has driven program decisions.

  • Proven ability to lead, develop, and motivate a team of scientists in a fast-paced research environment.

  • Deep scientific background in biochemistry, biophysics, and/or cell biology to guide assay strategy and compound optimization.

  • Strong cross-functional collaboration skills; ability to build productive relationships across disciplines.

  • Team player with a positive, can-do attitude and a commitment to scientific rigor, integrity, and Lilly's cultural values.

  • Experience managing direct reports in a pharmaceutical or biotechnology drug discovery setting.

  • Familiarity with AI/ML tools and laboratory automation platforms.

  • Broad experience across multiple modalities or therapeutic areas is a plus.

Physical Demands / Travel

The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Work Environment

This is an onsite position located in San Francisco, CA.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

*To perform this job successfully, an individual must be able to perform the role and responsibilities satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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

$163,500 - $281,600

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.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876