Company: Eli Lilly
Posted on: September 20, 2022
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 35,000 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.
At Lilly, we serve an extraordinary purpose. We make a difference
for people around the globe by discovering, developing and
delivering medicines that help them live longer, healthier, more
active lives. Not only do we deliver breakthrough medications, but
you also can count on us to develop creative solutions to support
communities through philanthropy and volunteerism.
Position Brand Description:
Provides technical support to achieve the reliable and compliant
manufacture of bulk drug substance to predetermined global quality
standards via a detailed set of manufacturing instructions and
- Understand the scientific principles required for manufacturing
intermediates, bulk drug substance, and drug product including the
interaction of the chemistry and equipment.
- Ensure that an accurate instruction set (tickets & procedures)
and PFD describe the process as performed and the control strategy
for the discrete manufacturing steps.
- Develop, monitor and appropriately react to established
statistically based 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.
- Prepare, review, approve, and provide technical support for
preparation of relevant technical documents, as required, such as:
change controls, regulatory submissions, deviation investigations,
validation protocols and summary reports, processing records,
procedures, PFDs, VMPs, etc. Participate in development and
implementation of process improvements, including capital
expansions and technical projects. Work within or lead
cross-functional teams in positive fashion to implement TS/MS
objectives and deliver on business plan and quality
- Serve as technical mentor for TS/MS Scientists and PDTs,
Managers and other disciplines.
- Support and/or lead technical projects (experimental, modeling
and/or production data analysis) to improve process control, yield,
purity, and/or productivity.
- Provide support to the global and local Post Launch
Optimization teams.Basic Requirements:
- Bachelor's or equivalent in scientific disciplines of
Biochemistry, Protein Chemistry, Biophysical Chemistry,
Bioanalytical Chemistry, Microbiology, Analytical Chemistry or
- Relevant industrial experience (greater than 5 years) in any of
the following associated disciplines such as Protein Manufacturing,
Quality Control, Quality Assurance, Advanced Project Management,
Regulatory, Development, or Administration.Additional Preferences:
- Technical/Scientific knowledge
- Decision making
- Ability to influence groups and communication skills
- Computer skills
- Problem solving
- Teamwork and interpersonal skills
- Clear understanding of cGMPs
- Mentoring Leadership
- Good written and oral communicationsEli Lilly and Company,
Lilly USA, LLC and our wholly owned subsidiaries (collectively
"Lilly") are committed to help individuals with disabilities to
participate in the workforce and ensure equal opportunity to
compete for jobs. If you require an accommodation to submit a
resume for positions at Lilly, please email Lilly Human Resources (
Lilly_Recruiting_Compliance@lists.lilly.com ) for further
assistance. Please note This email address is intended for use only
to request an accommodation as part of the application process. Any
other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and does not
discriminate on the basis of age, race, color, religion, gender,
sexual orientation, gender identity, gender expression, national
origin, protected veteran status, disability or any other legally
Our employee resource groups (ERGs) offer strong support networks
for their members and help our company develop talented individuals
for future leadership roles. Our current groups include: Africa,
Middle East, Central Asia Network, African American Network,
Chinese Culture Network, Early Career Professionals, Japanese
International Leadership Network (JILN), Lilly India Network,
Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans
Leadership Network, Women's Network, Working and Living with
Disabilities. Learn more about all of our groups.
As a condition of employment with Eli Lilly and Company and its
subsidiaries in the United States and Puerto Rico, you must be
fully COVID-19 vaccinated and provide proof of vaccination
satisfactory to the company (subject to applicable law).
Keywords: Eli Lilly, Carmel , Scientist, Other , Carmel, Indiana
Didn't find what you're looking for? Search again!