Eric Kamer Email & Phone Number
@lilly.com
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Who is Eric Kamer? Overview
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Eric Kamer is listed as Clinical Development Manager at Eli Lilly and Company, based in Indianapolis, Indiana, United States. AeroLeads shows a work email signal at lilly.com and a matched LinkedIn profile for Eric Kamer.
Eric Kamer previously worked as Director - Pharma Project Management @ LCCI at Eli Lilly And Company and Pharmaceutical Project Manager at Eli Lilly And Company. Eric Kamer holds Bachelor'S Degree, Chemical Engineering from Rose-Hulman Institute Of Technology.
Email format at Eli Lilly and Company
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AeroLeads found 1 current-domain work email signal for Eric Kamer. Compare company email patterns before reaching out.
About Eric Kamer
Eric Kamer is a Clinical Development Manager at Eli Lilly and Company. He possess expertise in financial audits, managerial finance, financial reporting, accounting, internal controls and 22 more skills. He is proficient in French.
Listed skills include Financial Audits, Managerial Finance, Financial Reporting, Accounting, and 23 others.
Eric Kamer's current company
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Eric Kamer work experience
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Director - Pharma Project Management @ Lcci
Current
Pharmaceutical Project Manager
Current
Technical Services / Manufacturing Sciences Team Leader
Operations Team Leader
- Responsibilities:Responsible for helping the process team achieve the safety, quality, and customer service targets. Acting leader of local safety team, daily production and bi-weekly process team meetings..
- Supported the process team in achieving customer service targets (> 100 million insulin devices per year) while limiting the number of safety and quality events
- Managed process changes that reduced potential product mix-up events by 40%
- Managed device sampling change that standardized and optimized batch release testing in addition to reducing waste (50,000 devices not being incinerated) and providing savings ($325,000/year + 1,500 hours/year)
- Oversaw three support team members with the execution of key operational deliverables
- Drove the reduction/elimination of high-risk ergonomic tasks within the production process
Sr. Engineer - Process, Indianapolis Parenteral Device Assembly And Packaging
- Responsibilities:Responsible for maintaining the reliable operation and qualified state of Parenteral Packaging Lines. Ensured that the equipment was in-control, compliant, and capable of meeting operations’ needs.
- Utilized production data to increase the mean time between failures on the parenteral packaging lines
- Supported the implementation of serialization on parenteral packaging lines
- Managed the pallet pattern adds to increase the amount of bulk package insulin per pallet
- Managed the implementation of a new vision system to reduce obsolete equipment and increase the range of cap colors that could be used for vial products
- Supervised engineering intern through the continuous improvement process
Engineering Intern Coordinator
- Responsibilities:Co-managed the engineering intern program for the manufacturing and development facilities.Accomplishments:
- Provided a holistic experience for the interns by exposing them to the culture, the facilities, the career paths, and Indianapolis.
- Led a developmental supervisor / mentor training to be used as an instructional aide for the program.
- Led/managed the program's steering team.
- Utilized the programs' resources (personnel and financial) effectively and efficiently.
- Participated in recruiting and HR activities to recruit and place interns as well as make offers for full-time positions.
Bioproduct Research And Development Engineer
- Responsibilities:Responsible for the process development of multiple large molecule (monoclonal antibody) projects. Collaborated with manufacturing (engineering, tech services, and quality) and development.
- Successfully supported internal and external manufactures to supply drug product for Phase 1/2 and Phase 3 clinical trial studies
- Improved the demonstration manufacture design to allow for the finished product to support method qualification as well as shelf-life dating
- Facilitated process risk assessments to build the process development plan for three different molecules
- Re-designed the drug product compatibility studies to provide a linkage to the manufacturing facility / process, to lessen the analytical burden, and to ensure repeatability.
- Validated a new freeze-thaw container for the use in the drug product manufacturing process.
Engineering Intern-Bioproduct Research And Development
Production Engineering Intern
Eric Kamer education
Bachelor'S Degree, Chemical Engineering
Bachelor Of Science (B.S.), Chemical Engineering
Frequently asked questions about Eric Kamer
Quick answers generated from the profile data available on this page.
What company does Eric Kamer work for?
Eric Kamer works for Eli Lilly and Company.
What is Eric Kamer's role at Eli Lilly and Company?
Eric Kamer is listed as Clinical Development Manager at Eli Lilly and Company.
What is Eric Kamer's email address?
AeroLeads has found 1 work email signal at @lilly.com for Eric Kamer at Eli Lilly and Company.
Where is Eric Kamer based?
Eric Kamer is based in Indianapolis, Indiana, United States while working with Eli Lilly and Company.
What companies has Eric Kamer worked for?
Eric Kamer has worked for Eli Lilly And Company and Perrigo.
How can I contact Eric Kamer?
You can use AeroLeads to view verified contact signals for Eric Kamer at Eli Lilly and Company, including work email, phone, and LinkedIn data when available.
What schools did Eric Kamer attend?
Eric Kamer holds Bachelor'S Degree, Chemical Engineering from Rose-Hulman Institute Of Technology.
What skills is Eric Kamer known for?
Eric Kamer is listed with skills including Financial Audits, Managerial Finance, Financial Reporting, Accounting, Internal Controls, Ifrs, Business Strategy, and Financial Analysis.
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