Senior Scientist -Manufacturing Science - Indianapolis, IN | Biospace
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Senior Scientist -Manufacturing Science

Eli Lilly and Company

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Location:
Indianapolis, IN
Posted Date:
7/12/2017
Position Type:
Full time
Job Code:
30043BR
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:
Biochemistry, Biology, Chemical Engineering, Chemistry, Manufacturing, Pharmaceutical, PhD, Technical Services,

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 39,000 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.

*Responsibilities  
How would you like a career where you get to use your best technical and analytical skills in a global scientific leadership role?  We are seeking a new scientific leader on our Parenteral Product Network Technical Services /Manufacturing Science (TS/MS) team.  Bring your skills and talents to our TS/MS organization where you’ll have the opportunity to make an impact on the lives of patients around the globe.

In this role, you are critical to the success of Lilly’s monoclonal antibody and biomolecule manufacturing.  As a Global Product Steward, you are a key member on our TS/MS cross-functional team and are responsible to provide product technical stewardship across multiple manufacturing sites, and to commercialize our strong pipeline portfolio of new parenteral products.  In addition, you will be responsible to design and implement global technical improvement projects for the Lilly bioproduct portfolio.  

In this Global Product Steward scientist role, you will have the opportunity to collaborate with cross-functional teams across Lilly and external manufacturing organizations.  As an individual contributor, you will work side-by-side with other Lilly professionals to drive the drug product technical agenda, including the exciting journey of new pipeline products from development into manufacturing.   You will provide influence, both on and off the manufacturing floor, by mentoring junior technical associates.  

Additional Information  
•Recognition and future promotion on the Technical Ladder
•10-20% domestic and international travel
•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 protected status.

Requirements

*Basic Qualifications  
•A degree in relevant area such as Biochemistry, Chemistry, Chemical Engineering, Biology or Pharmaceutical Science with one of the following:
?PhD degree with 3 years of practical experience of parenteral product manufacturing or
?Master degree with 8 years of practical experience of parenteral product manufacturing or
?Bachelor degree with 10 years of practical experience of parenteral product manufacturing
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) for this employment position.  

Additional Skills/Preferences  
We want you to bring your biomolecule expertise and technical influence to lead the manufacturing of medicine.  Candidates with parenteral drug product manufacturing experience and previous formulation and/or process development work are preferred.  We’re also excited if you bring an insatiable desire to learn, to innovate and to challenge yourself for the benefit of patients.