Address
Form of workScientist Chemistry
Mount Vernon, IN
3+ Month Contract
Micro lab on day shift only.
Job Responsibilities:
Performs data review activities as required.
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.
Writes and executes laboratory investigations for known lab 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.
Trains QC employees in good analytical techniques, methods and instrumentation based on expertise.
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.
The role may include shift and weekend work.
Performs testing on a range of samples, including finished products, water, and environmental samples.
May perform sampling activities of various types in the facility (e.g., swabs.).
Dispose of flammable materials in the accumulation container.
Maintains and troubleshoots testing equipment.
Provides and follows up on ideas for continuous improvements in laboratory processes.
Performs project work.
Trains QC employees in GMP, SHE, QC methods and processes.
Troubleshoots methods and processes.
May serve as an expert in a specific area of laboratory equipment, process, or system.
Typical Accountabilities:
Conduct activities and interactions consistent with Company values and in compliance with the Code
of Ethics and supporting Policies and Standards relevant to your role. Complete all required training on the Code of Ethics and supporting Policies and Standards on time.
Report potential issues of
non-compliance.
Ensures compliance with Corporate Policies and Directives, site Standard Operating Procedures,
site policies, work instructions, regulatory requirements, and industry best practice (cGMPs, GAMP,
ITIL, PMI).
Maintains a safe work environment and performs work in accordance with site, Safety, Health, and
Environment (SHE) policies and procedures.
Immediately report potential unsafe conditions to management.
Supports internal, external, and regulatory inspections including FDA, EMEA, and third-party
inspections
Participates in the investigation and resolution of product quality problems
Education, Qualifications, Skills and Experience-
Essentials: Bachelor degree or a minimum of 3 years of
demonstrated relevant experience in Quality Control
lab setting.
Desirable: Bachelor of Science degree, preferably
in Microbiology or a related discipline.
2 years laboratory experience.
High level of knowledge and
competence with a specific piece of
laboratory equipment, or a QC/QA
process or system.
M - F 9 - 5
Mount Vernon, IN
3+ Month Contract
Micro lab on day shift only.
Job Responsibilities:
Performs data review activities as required.
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.
Writes and executes laboratory investigations for known lab 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.
Trains QC employees in good analytical techniques, methods and instrumentation based on expertise.
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.
The role may include shift and weekend work.
Performs testing on a range of samples, including finished products, water, and environmental samples.
May perform sampling activities of various types in the facility (e.g., swabs.).
Dispose of flammable materials in the accumulation container.
Maintains and troubleshoots testing equipment.
Provides and follows up on ideas for continuous improvements in laboratory processes.
Performs project work.
Trains QC employees in GMP, SHE, QC methods and processes.
Troubleshoots methods and processes.
May serve as an expert in a specific area of laboratory equipment, process, or system.
Typical Accountabilities:
Conduct activities and interactions consistent with Company values and in compliance with the Code
of Ethics and supporting Policies and Standards relevant to your role. Complete all required training on the Code of Ethics and supporting Policies and Standards on time.
Report potential issues of
non-compliance.
Ensures compliance with Corporate Policies and Directives, site Standard Operating Procedures,
site policies, work instructions, regulatory requirements, and industry best practice (cGMPs, GAMP,
ITIL, PMI).
Maintains a safe work environment and performs work in accordance with site, Safety, Health, and
Environment (SHE) policies and procedures.
Immediately report potential unsafe conditions to management.
Supports internal, external, and regulatory inspections including FDA, EMEA, and third-party
inspections
Participates in the investigation and resolution of product quality problems
Education, Qualifications, Skills and Experience-
Essentials: Bachelor degree or a minimum of 3 years of
demonstrated relevant experience in Quality Control
lab setting.
Desirable: Bachelor of Science degree, preferably
in Microbiology or a related discipline.
2 years laboratory experience.
High level of knowledge and
competence with a specific piece of
laboratory equipment, or a QC/QA
process or system.
M - F 9 - 5
