Scientist, Dissolution & Biopharmaceutical Modeling

BioSpace; Indianapolis (IN); On-site; USD 65,000 - 149,000; Full time

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Medical, Dental, Vision benefits

Flexible benefits

Life insurance

Job summary

Lilly is seeking a dedicated scientist on site at our LTC-N Campus in Indianapolis to advance analytical method development for early clinical formulation development of synthetic drug molecules. You will collaborate across disciplines to guide formulation selection, characterize drug products, and mitigate program risks.

This role requires leadership, strong communication, and a track record in GLP/GMP contexts, with a commitment to safety and regulatory compliance in drug development for

Qualifications

• B.S. in Chemistry, Biochemistry, Pharmaceutical Science, or other directly related discipline (e.g., Material Science).
• Understanding of analytical techniques and methods for characterizing physicochemical properties of drug molecules and performance of drug products (e.g., HPLC, UV, NIR, dissolution).
• Strong leadership, supervisor, teamwork, communication and writing skills.

Responsibilities

• Develop analytical methods and conduct experiments to aid early clinical formulation development for drug delivery of various synthetic molecules.
• Collaborate with formulation scientists to design experiments and guide selection/characterization of formulations for pre-clinical and early clinical candidates.
• Partner with biopharmaceutical modeling scientists, analytical chemists, pharmaceutical scientists, and engineers to identify appropriate drug form, formulation, and process characteristics for drug product performance.
• Identify and mitigate technical risks for performance and production of clinical and commercial drug products.
• Execute with attention to safety, quality, regulatory, GLP/GMP, and legal requirements for all activities.
• Author key regulatory documents, demonstrating understanding of product performance control strategy and risk mitigation for clinical trials and commercialization.
• Embrace diverse thought and experience to deliver innovative solutions.
• Possess strong communication (oral, written), organizational, and leadership skills.
• Engage external scientific community to foster collaborations and advance Lilly’s portfolio.

Skills

Analytical chemistry

Leadership

Regulatory knowledge

Communication skills

GLP/GMP knowledge

Education

B.S. in Chemistry, Biochemistry, Pharmaceutical Science, or related discipline

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.

Organization And Position Overview

At Lilly, Synthetic Molecule Design and Development (SMDD) is involved in key activities for the development of synthetic active pharmaceutical ingredients from pre-clinical phases through commercialization of drug substances and drug products. Our scientists and engineers develop key technical and business solutions across the portfolio using their deep technical expertise to accelerate testing of clinical hypothesis and overall drug development. SMDD delivers on these responsibilities by recognizing diverse talent and cultures are necessary to bring the next generation of life-changing medicines to patients.

Responsibilities

• Developing analytical methods and conducting experiments to aid early clinical formulation development to enable drug delivery of a broad range of synthetic drug molecules.
• Collaborating with formulation scientists to design experiments and guide selection and characterization of formulations for pre-clinical and early clinical drug candidates.
• Partnering with biopharmaceutical modeling scientists, analytical chemists, pharmaceutical scientists, and engineers to identify the appropriate drug form, formulation, and process characteristics that provide the desired drug product performance.
• Identifying and mitigating technical risks for the performance and production of clinical and commercial drug products.
• Executing with attention to safety, quality, regulatory, GLP/GMP, and legal requirements for all activities.
• Authoring key regulatory documents, demonstrating appropriate understanding of product performance control strategy, and biopharmaceutics risk mitigation for clinical trials and product commercialization.
• Embrace diverse thought, background, and experience to deliver innovative solutions.
• Possess strong communication (oral, written), organizational, and leadership skills.
• Engaging and influencing the external scientific community to foster collaborations for innovation and to advance Lilly’s internal portfolio.

Basic Requirements

• B.S. in Chemistry, Biochemistry, Pharmaceutical Science, or other directly related discipline (e.g., Material Science)
• Understanding of analytical techniques and methods for characterizing physicochemical properties of drug molecules and performance of drug products (e.g., HPLC, UV, NIR, dissolution)
• Strong leadership, supervisor, teamwork, communication and writing skills.
• Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Skills/Preferences

• Industry, research or internship experience relevant to the position is strongly preferred.
• Knowledge of biopharmaceutics and pharmacokinetic principles, formulation development and pharmaceutical material sciences, and drug product factors impacting in vivo performance and manufacture.
• Basic understanding of regulatory aspects pertaining to development and clinical testing of drug products.
• General understanding of techniques and instrumentation used in characterization of pharmaceutical drug products, especially dissolution and other product performance tests.

Other Information

• This position will be on our LTC-N Campus in Indianapolis, IN
• Travel: 0-10%

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 (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 $65,250 - $148,500. 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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