Chemist - 3rd Shift

RIM Recruitment Professionals

Milwaukee (WI)

Sur place

USD 34 000 - 48 000

Plein temps

14 jours+

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Résumé du poste

RIM Recruitment Professionals in Milwaukee, WI seeks a Chemist on 3rd shift to interpret chromatography and analytical data, support GMP documentation, and contribute to method development and validation.

You will perform release and in-process testing, maintain compliant records, and collaborate with quality and manufacturing teams to ensure timely results. Requires a Bachelor’s in Chemistry and 2–3 years of industrial chemistry experience; GMP experience preferred.

Qualifications

  • Bachelor’s degree in Chemistry, Biochemistry, Biology, or related scientific discipline.
  • 2–3 years of industrial chemistry experience in QC or analytical lab.
  • Experience with analytical instrumentation.
  • Ability to interpret chromatography and analytical data.
  • Experience working within GMP or other regulated quality system.
  • Ability to write procedures, test methods, protocols, reports, and specifications.

Responsabilités

  • Perform release and in-process testing of raw materials, intermediates, test materials, and finished products.
  • Follow procedures, specifications, and test methods while ensuring compliance with internal and regulatory requirements.
  • Perform wet chemistry and analytical chemistry techniques to support quality control activities.
  • Interpret chromatography data and analytical results using applicable laboratory data management systems.
  • Assess analytical results against specifications and support material release decisions.
  • Perform and review critical and complex calculations associated with analytical testing and data evaluation.
  • Prepare and standardize volumetric solutions for routine and non-routine testing.
  • Maintain complete, accurate, and compliant GMP laboratory documentation.
  • Perform routine maintenance and basic troubleshooting of laboratory instrumentation.
  • Review calculations and analytical data associated with validation activities.
  • Provide analytical information and documentation to support customer complaints, returns, and investigations.
  • Write and revise procedures, test methods, protocols, reports, and material specifications.
  • Participate in training and provide guidance to support consistent laboratory compliance.
  • Meet established testing schedules and quality control deadlines.
  • Progress through a structured training program from supervised testing to independent execution of analytical methods.
  • Maintain laboratory supplies and ensure proper setup and use of analytical equipment.
  • Lift up to 25 pounds as needed to handle laboratory materials, reagents, and equipment.
  • Collaborate with other laboratory personnel and cross-functional teams in both laboratory and manufacturing environments.

Connaissances

Analytical chemistry
Chromatography data interpretation
Mathematical calculations
Attention to detail
Team collaboration
GMP compliance
Volumetric solutions

Formation

Bachelor’s degree in Chemistry

Outils

Analytical instrumentation

Description du poste

Chemist - 3rd Shift The Chemist will interpret chromatography and analytical data, maintain accurate GMP documentation, support laboratory investigations, and contribute to method development, validation, and continuous improvement initiatives.

Responsibilities

Perform release and in-process testing of raw materials, intermediates, test materials, and finished products in accordance with written methods and procedures. Follow applicable procedures, specifications, and test methods while ensuring compliance with internal and regulatory requirements. Perform wet chemistry and analytical chemistry techniques to support quality control activities. Interpret chromatography data and analytical results using applicable laboratory data management systems. Assess analytical results against specifications and support material release decisions. Perform and review critical and complex calculations associated with analytical testing and data evaluation. Prepare and standardize volumetric solutions for routine and non-routine testing. Maintain complete, accurate, and compliant GMP laboratory documentation. Perform routine maintenance and basic troubleshooting of laboratory instrumentation. Review calculations and analytical data associated with validation activities. Provide analytical information and documentation to support customer complaints, returns, and investigations. Write and revise procedures, test methods, protocols, reports, and material specifications. Participate in training and provide guidance to support consistent laboratory compliance. Meet established testing schedules and quality control deadlines. Progress through a structured training program from supervised testing to independent execution of analytical methods. Maintain laboratory supplies and ensure proper setup and use of analytical equipment. Lift up to 25 pounds as needed to handle laboratory materials, reagents, and equipment. Collaborate with other laboratory personnel and cross-functional teams in both laboratory and manufacturing environments.

Qualifications

Bachelor’s degree in Chemistry, Biochemistry, Biology, or a related scientific discipline. 2–3 years of industrial chemistry experience, preferably within a quality control or analytical laboratory. Experience with analytical instrumentation. Ability to accurately interpret chromatography and analytical data. Strong mathematical and analytical calculation skills. Experience working within GMP or another regulated quality system. Experience preparing and standardizing volumetric solutions and performing wet chemistry techniques. Ability to write clear procedures, test methods, protocols, reports, and specifications. Ability to perform routine instrument maintenance and basic troubleshooting. Ability to evaluate analytical results against established specifications. Strong attention to detail and commitment to quality. Ability to work collaboratively in a laboratory and manufacturing environment. #RIMUS

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