Lilly
healthcare
SeniorScientist-TSMS
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“Senior Scientist - TSMS at Lilly. Skills: technical oversight and stewardship for peptide manufacturing processes, resolution of technical issues, cGMPs, pharmaceutical manufacturing. Provide technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. Process monitoring”
What You'll Achieve.
achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards; Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state; Influence and implement the network technical agenda
Industry & Context.
Leads resolution of technical issues including those related to control strategy and manufacturing
Some travel (<25%) is required, Some off-shift work (night/weekend) may be required to support 24/7 operations, Qualified candidates must be legally authorized to be employed in the United States, Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status)
What They're Looking For.
Must Have
Bachelors in scientific disciplines of Chemistry, Biochemistry, Biology, Pharmacy, or Engineering, 3+ years of demonstrated experience and proficiency with pharmaceutical manufacturing, working knowledge of regulatory expectations
Nice to Have
Chemistry/Biochemistry strongly preferred, Knowledge and experience with Regulatory requirements, Knowledge of data management practices across manufacturing, Enthusiasm for changes, team spirit and flexibility, Ability to influence and communicate to diverse groups on business, or technical issues within the site and function, Proficiency in delivering complex tasks and/or tasks that are cross-functional, Demonstrated Project Management skills and ability to coordinate complex projects
What You'll Do.
Provide technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards
Improvements where necessary
Provide technical oversight and stewardship for peptide manufacturing processes
Leads resolution of technical issues including those related to control strategy and manufacturing
Ensure proper characterization of processes and products
Ensure effective documentation of the process description
and specifications (and the justification of these measures
Ensure that processes are compliant
and maintained in a validated or qualified state
justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose
Influence and implement the network technical agenda and drive continuous improvement
Maintaining peptide processes in a state of compliance with US and global regulations
How You'll Work.
Team & Collaboration
Interacts daily with a wide variety of people, primarily external partners team members and site management; working cross-functionally within the site and other functions to deliver on technical objectives; Build and maintain relationships with development and central technical organizations; Operate with ‘Team Lilly’ in mind
Communication Scope
Employ excellent communication skills to manage internal and external relationships; Ability to influence and communicate to diverse groups on business, or technical issues within the site and function
Process & Methodology
Demonstrated Project Management skills and ability to coordinate complex projects
Full 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. Organization Overview: Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API EM TS/MS Sr. Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Sr. Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners team members and site management. The candidate will be responsible for process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives. Key Objectives/Deliverables: * Provide technical oversight and stewardship for peptide manufacturing processes. * Leads resolution of technical issues including those related to control strategy and manufacturing. * Empl
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