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8471 Process Design Engineer jobs in Indianapolis,IN

New, Posted just now

Warehouse Associate

REVISED PERSONNEL

Indianapolis, IN 46227

Onsite

Able to operate RFGen Gun.
Able to operate forklift safely.
Twisting/Bending: Must be able to twist/bend 50% of the day.
Sitting: Must be able to sit 20% of the day.
Squatting, Climbing and/or Crawling: Must be able to squat/climb/crawl 20% of the day.
High School Diploma or equivalent
Able to communicate both in writing and verbally.
Push/Pull: Must be able to push/pull 50 pounds.
Able to utilize math to perform basic inventory counts.
Able to read and interpret directions and order details.
Must pass pre-employment physical.
Stand: Must be able to stand 80% of the day.
Lift: Must be able to lift and/or carry a minimum of 50 pounds.

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Manufacturing Engineer - Assembly

Rolls-Royce

Indianapolis, IN 46241

HybridEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

PhD with experience in Manufacturing or Assembly Engineering
Bachelor's degree with 2+ years of experience in Manufacturing or Assembly Engineering
Associate's degree with 5+ years of experience in Manufacturing or Assembly Engineering
Masters degree with experience in Manufacturing or Assembly Engineering
In order to be eligible for consideration, you must be a U.S. Citizen

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Associate Director - Global Process Automation and Control Engineering (Corporate)

Eli Lilly

Indianapolis, IN 46262

Health InsurancePaid Time OffRetirement Benefit

Project Manager-Design and Construction

IU Health

Indianapolis, IN 46262

New, Posted 19 hours ago

Technical Sourcer - Design

Virtual Vocations

Indianapolis, IN 46262

Director, Analytical Chemistry Extended Characterization

Eli Lilly and Company

Indianapolis, IN 46227

Onsite

Experience developing global regulatory strategies including authoring regulatory submissions, responding to regulatory questions, and/or registering products across global markets
PhD in analytical chemistry or bioanalytical chemistry, or a related field with 10+ years of experience in the pharmaceutical industry
Experience with technical transfer of analytical methods into manufacturing operations
Prior laboratory operations and management experience leading a team of scientists and associates for analytical development in a clinical stage biotech environment
Travel: 15-30% (initial 4‑6 months travel to Verve Boston site required)
Prior experience must include performing analytical assays to support the development of lead molecules, troubleshooting and optimizing analytical assays for GMP use per ICH guidelines
Conceptual understanding of solid phase oligonucleotide synthesis and purification strategies
Experience with analytical control strategy implementation, and/or regulatory submissions related to advanced gene therapies
Demonstrated success in persuasion, influence, and negotiation
Direct experience analyzing LNPs and RNA by biophysical techniques such as LC‑MS, DSC, DLS, MALS, etc.
Experience with planning and executing product and process development studies such as forced degradation, comparability assessments, stability, extended characterization, etc.
Ability to prioritize multiple activities and manage ambiguity
Ability to influence others to promote a positive work environment
Demonstrated competency in operating HPLC/UPLC/LC‑MS instrumentation
Good interpersonal skills and a sustained tendency for collaboration
Hands‑on experience analyzing DNA/RNA by IP‑RP, IEX, LC‑fluor and multi‑modal LC techniques required
Demonstrated technical proficiency and ability to create ideas for future work plans