Tim Davis

Tim Davis Email and Phone Number

Manufacturing Director | cGMP | Pharmaceutical | Medical Device | I help regulated companies improve manufacturing efficiencies through leadership, kaizen, Lean, and 6-sigma that has resulted in $20MM in cost savings @ Elanco
greenfield, indiana, united states
Tim Davis's Location
Brownsburg, Indiana, United States, United States
About Tim Davis

I am currently based in Indianapolis, Indiana and have broad extensive professional experience managing a variety of complex operations in pharmaceutical, medical device, chemical, and food industries. I have been responsible for operations as large as 450 people and $500 million in revenue and delivered cost savings of over $20 million through organizational changes and efficiency improvements. I have a hands-on understanding not limited to: Solid dose, liquid formulations, sterile injectables and IV solutions, clean room operations, API and chemical production, electrical/mechanical medical devices, injection molding, industrial chemical blends and reactions, as well as specialty oil blends. AREAS OF EXPERTISE:• Organizational and process Improvements • Team building & development • Aseptic & Parenteral Experience • People leadership • P & L responsibility• Consolidations and Integrations• Strategic decision making• Training & Mentoring • API production experience• Packaging experience• Liquid Handling• cGMP and regulatory complianceContact information - tedavis0001@gmail.com

Tim Davis's Current Company Details
Elanco

Elanco

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Manufacturing Director | cGMP | Pharmaceutical | Medical Device | I help regulated companies improve manufacturing efficiencies through leadership, kaizen, Lean, and 6-sigma that has resulted in $20MM in cost savings
greenfield, indiana, united states
Website:
elanco.com
Employees:
7176
Tim Davis Work Experience Details
  • Elanco
    Director - Manufacturing Api
    Elanco Nov 2024 - Present
  • Medtronic
    Manufacturing Director (Plant Manager)
    Medtronic Nov 2016 - Jul 2024
    Plainfield, In
    Led 225-person Plainfield plant with P/L responsibility ($37M budget), safety/quality/regulatory performance that assembles, manufactures, repairs, refurbishes, packages medical devices in a cGMP environment for Medtronic. Key contact for Medtronic Indiana including state and federal government; interface with senators and other officials.• Oversaw contract manufacturing operations of $100M ablation product business spanning 5 plants and over 15 vendors. Reduced manufacturing time from 3 months to 30 days by working with vendors. • Reduced recordable safety rate from 5 per year down to 0 by instituting safety awareness programs and OSHA education.• Developed and presented divestiture plan for executive management approval involving comprehensive assessment to impact finances, personnel, and inventory, resulting in modifications by buyer and ultimate approval to proceed along with developing of an OPEX strategy for cost reductions at the site.
  • Medtronic
    Sr. Operations Manager
    Medtronic Jan 2010 - Nov 2016
    Crystal Lake, Il
    Governed overall operations including safety, quality, and other performance metrics, and financial performance ($85M budget) of 250-person production department producing, assembling, and packaging injection molded medical devices in a cGMP environment for Sharps disposal containers and syringe product lines for both branded and contract manufacturing. • Increased OEE 15% by reduced headcount, prioritized roles through cross training, established kanbans and pull systems; strengthened operations, upskilled operators, implemented new systems, and improved training resulting in reducing backorders from $1.6M to $150k in 8 months.• Minimized nonconformance rate (NCR) through CAPA from 30 to 3 per day in 3 months by updating batch record documents, changing cosmetic criteria, and conducting operator training.
  • Avatar Corporation
    Plant Manager
    Avatar Corporation Jun 2008 - Dec 2009
    University Park, Illinois, United States
    Oversaw safety, quality, cost, production, packaging, and delivery of pharmaceutical excipients, food additives, oil lubricants, and cosmetic wax products from raw material suppliers to customers within 110K sq. ft. cGMP plant, 52 employees, and COGS of $52M. • Developed plant operating budget and production metrics and communicated to employees.• Developed a safety training and awareness program to improve the safety culture and lower recordable incidents from RIR of 7 to RIR of 2.
  • Mallinckrodt Pharmaceuticals
    Operations Manager
    Mallinckrodt Pharmaceuticals May 2005 - Jun 2008
    Hobart, Ny
    Promoted to manage 4 fast-paced cGMP high-volume departments involving dispensing, blending, tableting, and packaging generic, branded, and contract pharmaceutical manufacturing in cGMP environment with $260M budget and 450 employees. • Increased production output 5%–10% YoY through staffing changes and installation of 2 packaging lines totaling $12M.• Worked with contract manufacturing customers to reduce changeover times from 6 to 4 hours by implementing Operational Excellence (Lean/Six-Sigma) tools to develop culture of continuous improvement; maintained budget YoY without increases based on continuous improvement.• Implemented quality projects to reduce nonconformances (NCR and CAPA) by 10%. Developed visual line clearance manual to reduce foreign tablet nonconformances from 15 to 1 per year.
  • Mallinckrodt Pharmaceuticals
    Production Superintendent
    Mallinckrodt Pharmaceuticals Jul 2004 - May 2005
    Paris, Ky
    Managed 2 chemical manufacturing and packaging departments with $3M budget. • Increased customer service from 78% to over 95% by initiating second shift in one department and converting another department to 24/7 operation to meet customer orders.
  • Abbott Laboratories
    Multiple Positions
    Abbott Laboratories 2000 - 2004
    Abbott Park, Il
    Nominated into Abbott’s managerial program (Engineering Professional Development Program). Positions held:• Quality Investigation Engineer over parenteral manufacturing – interfaced with FDA and made process changes through change management. Investigated nonconformances and ran CAPA investigations. • Chemical Manufacturing Project Manager - small molecule API production• Manufacturing Supervisor and Inventory Controller – small molecule API production and packaging• Production Engineer for packaging and labeling of pharmaceuticals• Process Support Engineer - Received Presidents Award by increasing small molecule API yields 10% and reducing time.
  • Dow
    Chemical Process Engineer
    Dow May 1995 - Dec 1997
    Midland, Michigan, United States
    Process Engineer over polymer reactions, blending, and processing - Implemented process improvements and qualified equipment

Tim Davis Education Details

Frequently Asked Questions about Tim Davis

What company does Tim Davis work for?

Tim Davis works for Elanco

What is Tim Davis's role at the current company?

Tim Davis's current role is Manufacturing Director | cGMP | Pharmaceutical | Medical Device | I help regulated companies improve manufacturing efficiencies through leadership, kaizen, Lean, and 6-sigma that has resulted in $20MM in cost savings.

What schools did Tim Davis attend?

Tim Davis attended University Of Chicago, University Of Louisville, University Of Louisville.

Who are Tim Davis's colleagues?

Tim Davis's colleagues are Katie Reigelsberger, Edyta B., Amanda Audsley, Ebru Akçay, Francisco Jose Alvarez Darriba, Stuart Adams, Stanislas Boulanger.

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