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.
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