Scientist Chemistry

Responsibilities:

• Excellent employment opportunity for a Scientist Chemistry in the Mt Vernon IN area.
  (onsite)
• 2nd shift: 12:00PM 10:30PM
• Perform qualitative and/or quantitative analytical chemistry testing on pharmaceutical raw materials components and/or finished products according to policy and procedures at consistently high levels with a focus on quality and efficiency (Role may include shift
  work).
• Participates in and may lead some QC Team Discussions.
• Maintains adequate inventories of reagents glassware and other supplies.
• Maintains current complete legible notebooks and laboratory records in compliance with good scientific and regulatory practices.
• Support testing for laboratory investigations of known laboratory errors and Out of Specification (OOS) results using the current electronic deviation system and/or other QC procedures.
• Participates in investigations for PET process areas related to QC processes or data.
• Troubleshoots methods and processes.
• Executes laboratory processes in compliance with GMPs site and corporate policies standard operating procedures (SOPs) and test methods.
• Immediately reports deviations that have the potential to compromise product quality.
• Performs testing on a range of samples including chemical raw materials components
  (including packaging materials) finished products stability samples water and environmental samples.
• May perform sampling activities of various types in the facility (e.g. swabs.).
• Dispose of flammable materials in the 90day accumulation container.
• Maintains and troubleshoots testing equipment.
• Provides and follows up on ideas for continuous improvements in laboratory processes.
• Performs project work.
• Troubleshoots methods and processes.
• May serve as an expert in a specific area of laboratory equipment process or system.

Experience:

• Bachelors Degree and 12 years of related experience.
• The incumbent is not necessarily performing all the Major Responsibilities of the role immediately.
• The incumbent may begin by specializing in one or more of these responsibilities whilst working to develop a solid knowledge of the process being supported and applicable cGMPs.
• Over time the incumbent will be expected to obtain the necessary training to become skilled in all major responsibilities of the role.