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John Bain

Laboratory Coordinator @ Nestle Professional Beverages

Manager, Quality Control at Cardinal Health

Indianapolis, Indiana

Ranked #150 out of 2,996 for Laboratory Coordinator in Indiana

Section title

John Bain's Email Addresses & Phone Numbers

John Bain's Work Experience

Nestle Professional Beverages

Laboratory Coordinator

2010 to 2010

Nestle Professional Beverages

Laboratory Coordinator

2010 to 2010

Cardinal Health

Manager, Quality Control

Indianapolis, Indiana

John Bain's Education

Ball State University

Master's Degree, Chemistry

1985 to 1987

Indiana University

Bachelor's Degree, Biochemistry

1981 to 1985

John Bain's Professional Skills Radar Chart

Based on our findings, John Bain is ...

Efficient
Determined
Strong sense of self

What's on John Bain's mind?

Based on our findings, John Bain is ...

57% Left Brained
43% Right Brained

John Bain's Estimated Salary Range

About John Bain's Current Company

Nestle Professional Beverages

Frequently Asked Questions about John Bain

What company does John Bain work for?

John Bain works for Nestle Professional Beverages


What is John Bain's role at Nestle Professional Beverages?

John Bain is Laboratory Coordinator


What is John Bain's personal email address?

John Bain's personal email address is jo****[email protected]


What is John Bain's business email address?

John Bain's business email address is j****[email protected]


What is John Bain's Phone Number?

John Bain's phone (317) ***-*635


What industry does John Bain work in?

John Bain works in the Pharmaceuticals industry.


About John Bain

đź“– Summary

Laboratory Coordinator @ Nestle Professional Beverages From 2010 to 2010 (less than a year) Laboratory Coordinator @ Nestle Professional Beverages From 2010 to 2010 (less than a year) Manager, Quality Control @ Cardinal Health • Oversees the laboratory systems to ensure that the data generated by the laboratories (Incoming materials, DS, DP, Release/ Stability) are produced in accordance with all applicable regulations and company policies and procedures• Develops and applies practices, which will enable the laboratory to meet and exceed, desired customer and regulatory standards in a cost effective fashion• Monitors quality assurance activities (Calibration, Maintenance, Method Transfer, etc.) in the laboratories to determine conformance with applicable procedures and good practices• Assists in and/or conduct all laboratory investigations of discrepancies to resolve problems and works with Management to ensure corrective action or preventive actions are implemented in a timely manner• Remains aware of developments in the analytical chemistry and microbiology by reading current technical literature and attending technical meetings• Makes recommendations to management to improve the performance of the laboratories• Advises in the purchase of those laboratory supplies which have a direct effect on quality• Develops and monitors key performance indicators for the laboratory and implements CAPA as needed• Executes or participates in internal and external laboratory quality audits, as directed by management• Assists in the training efforts of the laboratory personnel• Works closely with Operations regarding the interpretation and implementation of any element of the Quality Management System, to resolve differences, and ultimately to ensure that the system is understood and applied uniformly Indianapolis, IndianaTeam Coordinator, Equipment Validation @ Cook Pharmica • Mentor, lead and supervise a team of six salaried validation employees responsible for the qualification of pharmaceutical manufacturing equipment and quality control laboratory equipment.• Serve as the leader of a cross functional team commissioned to qualify laboratory equipment and associated systems in a cGMP environment.• Provide qualification strategy from a project management and technical standpoint.• Serve as the Project Manager for all Quality Control Laboratory systems (laboratory equipment and computer systems).• Utilize Microsoft Project to track project status.• Manage multiple projects to provide documented qualification of new manufacturing equipment and Quality Control Laboratory equipment.• Develop, review and approve lifecycle documents including impact assessments, user requirements specifications, component criticality assessments, installation and operational qualification protocols, summary reports and traceability matrices using Regulus/Syncade.• Develop and execute qualification protocols, analyze data and author summary reports using Regulus/Syncade.• Utilize TrackWise software to process Change Control, CAPA and/or Deviations. From January 2014 to October 2014 (10 months) Team Lead, Laboratory Systems Validation @ Cook Pharmica • Serve as the leader of a cross functional team commissioned to qualify laboratory equipment and associated systems in a cGMP environment.• Provide qualification strategy from a project management and technical standpoint.• Serve as the Project Manager for all Quality Control Laboratory systems (laboratory equipment and computer systems).• Utilize Microsoft Project to track project status.• Manage multiple projects to provide documented qualification of Quality Control Laboratory equipment.• Develop, review and approve lifecycle documents including impact assessments, user requirements specifications, component criticality assessments, installation and operational qualification protocols, summary reports and traceability matrices.• Develop and execute qualification protocols, analyze data and author summary reports.• Utilize TrackWise software to process Change Control, CAPA and/or Deviations. From July 2013 to January 2014 (7 months) Bloomington, Indiana AreaValidation Associate @ Cook Pharmica • Serve as lead Validation Associate for Quality Control Laboratory equipment qualification.• Manage multiple projects to provide documented qualification of Quality Control Laboratory equipment.• Develop and review lifecycle documents including impact assessments, user requirements specifications, component criticality assessments, risk assessments and traceability matrices.• Develop and execute qualification protocols, analyze data and author summary reports.• Utilize TrackWise software to process Change Control, CAPA and/or Deviations. From August 2011 to July 2013 (2 years) Bloomington, Indiana AreaQuality Associate - Methods Lead @ Eli Lilly and Company • Lead the deployment of the Method Management aspect of the Global Laboratory Information Management System (GLIMS) Project to the QC Labs around the world. Trained QC personnel across all Lilly QC labs in the use of Regulus (a.k.a. Syncade) for the business processes associated with analytical methods.• Assess each Quality Control Lab’s methods for compliance to GQS603, section 1.1.• Negotiate and coordinate site deployment/training visits (within the US and at international Lilly facilities) with appropriate personnel from the local site and other teams within the Global LIMS Deployment Group.• Create effective training presentations.• Equip site personnel with the knowledge of the Method Management Business Process through training and guidance.• Provide consultation (technical and strategic advice) to customers after deployment visit.• Negotiate Method Management Charter for each site as a means to define project scope and milestones.• Establish routine meetings with customers to monitor their progress against goal.• Raise awareness of issues encountered in the field to the owner of Method Management Business Process and that person’s team for the purpose of further refining that process. From May 2006 to May 2010 (4 years 1 month) Indianapolis, Indiana AreaProject Leader @ Eli Lilly and Company • Survey the Dry Products and Small Molecule Bulk Quality Control Laboratory networks and MS&T Molecule Stewards for analytical issues.• Develop process to capture findings of survey as well as an effective means to present findings to GQL Director.• Mentor, lead and supervise a chemist.• Engage appropriate resources to remediate methods and/or provide consultation to QC Lab customers. From March 2005 to May 2006 (1 year 3 months) Indianapolis, Indiana AreaLeader Cleaning Validation @ Eli Lilly and Company • Build Analytical Cleaning Validation Technical Knowledge Network.• Coordinate personnel from Analytical Development and their activities to support manufacturing as well as the remediation of analytical methods.• Mentor, lead and supervise a group of five chemists.• Provide technical advice and/or project coordination for a variety of clients.• Drive, facilitate and manage the transfer of 22 methods within 15 months. From January 2004 to March 2005 (1 year 3 months) Indianapolis, Indiana AreaAnalytical Chemist @ Eli Lilly and Company • Document the qualification of new instruments.• Coordinate personnel and activities for laboratory renovation on the Wet Chemistry/Metals laboratory of Environmental Analytical Services.• Mentor, lead and supervise a group of five laboratory technicians across two shifts in the Wet Chemistry/Metals laboratory of Environmental Analytical Services.• Provide technical advice and/or project coordination for a variety of clients.• Author laboratory standard operating procedures to be compliant with Environmental Protection Agency (EPA) recommendations.• Develop sample preparation methods.• Manage special projects. From September 2000 to December 2003 (3 years 4 months) Lafayette, Indiana AreaLead Scientist @ Indianapolis Power & Light Company • Develop, implement, monitor and oversee corporate Quality Assurance Plans pertinent to laboratory sampling and testing methods.• Resolve variety of scientific testing, sampling and quality matters pertaining to NPDES Permits, fuel (coal & fuel oil) quality, water quality and other miscellaneous issues.• Author and standardize laboratory test and quality assurance procedures for all five of IPL's laboratories.• Develop and establish all laboratory and sampling methods to conform to appropriate regulatory agency protocol.• Serve as the corporate advisor to all of IPL in scientific matters.• Prioritize, assign and supervise daily work of IPL's Central Laboratory.• Negotiate Laboratory Budget.• Write specifications for all laboratory equipment purchased as "Capitol Expense".• Develop and institute all laboratory data entry spreadsheets using MS Excel 97. From June 2000 to September 2000 (4 months) Indianapolis, Indiana AreaLaboratory Director @ City of Kokomo • Hire, train and manage Lab Staff of three.• Prioritize, assign and supervise daily work.• Develop and establish all laboratory and sampling methods to conform to appropriate regulatory agency protocol.• Employ statistical process control (SPC) in all process control spreadsheets for the Operations Division.• Advise wastewater plant Superintendent, Assistant Superintendent and Pretreatment Coordinator in scientific matters.• Develop and institute all laboratory data entry spreadsheets using MS Excel 97.• Negotiate Laboratory Budget.• Write specifications for all laboratory equipment purchased as “Capitol Expense”.• Monitor chemical substances in city’s environment.• Act as Quality Assurance Officer.• Perform Monthly Audit of Laboratory Data and Procedures.• Serve as Laboratory Inventory Clerk.• Interact with representatives of regulatory agencies to assure compliance with NPDES Permit Limits.• Expedite laboratory orders to scientific supply vendors. From June 1996 to June 2000 (4 years 1 month) Kokomo, Indiana AreaChief Chemist @ City of Muncie, Indiana • Act as Quality Assurance Officer.• Perform Quality Control on acquired data using Environmental Protection Agency protocol and a personal computer.• Operate Inductively Coupled Plasma (ICP) and Graphite Furnace.• Employ a variety of wet chemical tests.• Monitor chemical substances in city’s environment.• Advise staff on daily testing.• Assume primary responsibility in Lab Manager’s absence. From September 1988 to June 1996 (7 years 10 months) Muncie, Indiana Area


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In a nutshell

John Bain's Personality Type

Extraversion (E), Intuition (N), Thinking (T), Judging (J)

Average Tenure

2 year(s), 3 month(s)

John Bain's Willingness to Change Jobs

Unlikely

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