Advisor Engineer, Drug Product and Spray Drying Process Development - SMDD

BioSpace; Indianapolis (IN); Vor Ort; USD 129.000 - 209.000; Vollzeit

Benefits dieser Stelle

401(k)

Pension

Medical benefits

Bonus program

Zusammenfassung

Lilly seeks a highly qualified chemical engineer to advance drug product processes, with emphasis on amorphous solid dispersion technology, for Phase 2/3 through commercialization. You will design, scale up, and optimize ASD manufacturing processes and contribute to regulatory submissions.

Ideal candidates will have a PhD or MS/BS in chemical engineering or pharmaceutical science with extensive process development experience, and proven ability to collaborate across disciplines and sites at

Qualifikationen

• Ph.D. in Chemical Engineering, Pharmaceutical Sciences, or closely related STEM with 0-5 years of demonstrated experience in pharmaceutical process development.
• MS in Chemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or closely related STEM degree with 7+ years of demonstrated experience in pharmaceutical process development.
• BS in Chemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or closely related STEM degree with 10+ years of demonstrated experience in pharmaceutical process development.

Aufgaben

• Scale up ASD processes from lab to manufacturing.

Kenntnisse

Heat & mass transfer

Particle formation

Process scale‑up

ASD manufacturing

Tech transfer

Cross‑functional

Documentation

Ausbildung

Ph.D. in Chemical Engineering

MS in Chemical Engineering

BS in Chemical Engineering

Tools

PAT systems

Analytical instrumentation

Jobbeschreibung

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.

Position Brand Description

The Synthetic Molecule Design and Development (SMDD) department within Lilly Research Labs is involved in key activities for the advancement of small molecules, peptides, and oligonucleotides from early discovery phases to commercialization. Our scientists and engineers develop innovative technical and business solutions across a portfolio of projects using their deep technical expertise to accelerate testing of clinical hypothesis and overall drug development. Through recognizing the value of a hardworking, diverse, and inclusive workforce, SMDD delivers on these responsibilities and helps bring the next generation of life‑changing medicines to patients. Our team is seeking a highly motivated candidate to work on drug product process development, with a focus on amorphous solid dispersion manufacturing technologies such as spray drying and related particle engineering platforms, spanning Phase 2/3 clinical trials through registration and commercialization.

Responsibilities

Candidates must possess a strong background in chemical engineering fundamentals, including heat and mass transfer, particle formation, and process scale‑up, and be able to integrate this understanding with analytical and manufacturing considerations to advance drug product manufacturing processes. Specific responsibilities for this role include:

• Apply engineering fundamentals to design, scale up, and optimize amorphous solid dispersion (ASD) manufacturing processes, such as spray drying, hot melt extrusion, and/or coprecipitation, for producing drug product intermediates from lab and pilot scale through commercial manufacturing scale.
• Drive process development activities for drug product intermediates advancing toward commercialization, translating process and analytical understanding into a robust, scalable control strategy that supports commercial manufacturing readiness and regulatory filing.
• Support technology transfer and scale‑up of manufacturing processes to internal and external sites.
• Collaborate and communicate project specific challenges and opportunities with key partners, including external contract manufacturing organizations, to plan and manage short‑and long‑term development activities aligned with the global CMC strategy.
• Engage and influence internal and external scientific communities to solve technical challenges, identify and implement novel drug product manufacturing technologies, and inform process and control strategy decisions.
• Author and review high‑quality technical reports, peer reviewed publications, and regulatory documentation to support new technologies and regulatory submissions.

Basic Requirements

• Ph.D. in Chemical Engineering, Pharmaceutical Sciences, or closely related STEM degree with 0-5 years of demonstrated experience in pharmaceutical process development, or
• M.S. in Chemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or closely related STEM degree with 7+ years of demonstrated experience in pharmaceutical process development, or
• B.S. in Chemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or closely related STEM degree with 10+ years of demonstrated experience in pharmaceutical process development.

Additional Skills/Preferences

• Experience with process development and scale‑up of particle engineering and/or amorphous solids manufacturing technologies (e.g., spray drying process, hot melt extrusion, co‑precipitation, etc.).
• Experience in technical considerations for equipment design and integration, process monitoring, integration of process analytical technology (PAT) systems, and scientific approaches to control strategy. Involvement with process modelling and simulation programs for improved process and formulation understanding.
• Experience with technology transfer to external manufacturing partners and cross‑site process comparability.
• Experience supervising or guiding the work of other engineers or scientists.
• Excellent oral communication and documentation skills.
• Demonstrate ability to effectively collaborate with multidisciplinary teams.
• Demonstrate leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertainty

Additional Information

Possible exposure to chemicals, allergens, and loud noises.

Travel: 0 to 10%

Position Local: Onsite Monday through Friday, Indianapolis, IN; Lilly Technology Center‑North (LTC‑N)

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).

Lilly offers a comprehensive benefit program to eligible employees, including:

• 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)
• Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance)

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $129,000 - $209,000

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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