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Associate​/Sr. Associate Manufacturing Scientist - Molecule - Lebanon API

Job in Lebanon, Boone County, Indiana, 46052, USA
Listing for: BioSpace
Full Time position
Listed on 2025-12-19
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 66000 - 171600 USD Yearly USD 66000.00 171600.00 YEAR
Job Description & How to Apply Below
Position: Associate/Sr. Associate Manufacturing Scientist - Small Molecule - Lebanon API

Associate/Sr. Associate Manufacturing Scientist - Small Molecule - Lebanon API

Join to apply for the Associate/Sr. Associate Manufacturing Scientist - Small Molecule - Lebanon API role at Bio Space

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 Overview

Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly’s largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site, and the successful candidate will help to build the processes and systems to enable a successful startup into GMP manufacturing operations.

Responsibilities
  • Understand the scientific principles required for manufacturing intermediates and bulk drug substances, including the interaction of the chemistry and equipment.
  • Execute technical projects (experimental, modeling and/or production data analysis) to improve process control, yield, purity, and/or productivity.
  • Provide technical support for preparation of relevant technical documents, such as technical reports, change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs (Process Flow Documents), VMPs, etc.
  • Develop and monitor established metrics in real‑time to assess process variability and capability.
  • Understand, justify and document the state of validation (process and cleaning) with data that evaluate the capability of the manufacturing process to meet its stated purpose.
  • Ensure that an accurate instruction set (tickets & procedures) and PFD describe the process as performed and the control strategy for the discrete manufacturing steps.
  • Ensure that experiments are well designed with clear objectives.
  • Ability to analyze data and ensure appropriate documentation.
  • Write technical reports and documents.
Basic Requirements
  • Bachelor’s in STEM Discipline (Chemistry preferred)
  • 2+ years of experience in cGMP manufacturing (pharmaceutical manufacturing experience preferred)
Additional Preferences
  • Demonstrated understanding of process chemistry
  • Demonstrated basic knowledge in small molecule, peptide, or oligonucleotide API manufacturing
  • Relevant industrial experience in API manufacturing, TS/MS (Technical Services/Manufacturing Sciences), Quality Control, Quality Assurance, or Development
  • Familiarity with cGMP manufacturing environment and terminology

    Excellent analytical, interpersonal, written and oral communication skills
  • Ability to work on own initiative and as part of a Process Team consisting of a diverse group of management, production, science and engineering professionals
  • Creativity to identify improvement opportunities and the tenacity/initiative to see them implemented
  • Guidance/mentoring of others through processes
  • Flexibility to meet business needs

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600. 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…

Position Requirements
10+ Years work experience
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