Chemist 2 Quality Control

5 days ago


East Brunswick, New Jersey, United States USPL Nutritionals, LLC. Full time
Job Summary

We are seeking a highly skilled Chemist 2 to join our Quality Control team at USPL Nutritionals, LLC. The successful candidate will be responsible for performing routine analysis of samples, preparing reagents and standards, and verifying quality in accordance with statistical process control.

Key Responsibilities
  • Perform assigned sampling, physical, and chemical tests on raw materials, active dietary ingredients, in-process, finished, and stability products in a FDA GMP regulated lab environment.
  • Use a variety of wet chemicals, physical, and instrumental techniques, as well as routine QC instruments, including HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), and Potentiometer.
  • Work independently on HPLC and other QC instruments after skilled training.
  • Participate in troubleshooting of testing-related investigations to assist in determining the root cause of off-spec product results.
  • Ensure compliance with company and customer specifications, as well as federal, state, and local regulatory requirements.
  • Perform complicated testing with supervisory direction and document work clearly and accurately.
  • Record and report results as per GDP guidelines and procedures for all testing performed on a daily basis.
  • Prepare and/or review Test Procedures, SOPs, and Protocols as assigned.
  • Perform calibrations of laboratory instruments/equipment with supervisory direction/training, if required.
  • Comply with all regulatory/in-house requirements, including safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation, when performing assigned activities.
  • Operate Microsoft Word and Excel on a daily basis.
  • Assist junior staff in training on specific tests, instrument operation, and performing troubleshooting of test-related issues or instrument-related issues to the best available knowledge.
  • Must be able to work extended hours as needed and occasional weekends.
Requirements
  • BS in Chemistry or related scientific disciplines.
  • One (1) year of basic chemistry techniques (can be academic) is a plus.
  • Minimum of 3 years QC lab work experience in operating HPLC with industry experience in dietary supplements, food, or OTC manufacturing.
Preferred Skills and Abilities
  • Ability to maintain integrity and honesty at all times and to communicate with transparency.
  • Ability to work independently or as part of a team.
  • Solid understanding of cGMPs and GLP and familiarity with 21 CFR Part 11.
  • Strong working knowledge of Microsoft Word, Excel.
  • Good documentation practices and ability to write simple, clear reports.
  • Meets commitments on time and practices time-management skills.
  • Seeks to identify continuous improvement needs.
  • Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution, and Waters Empower Lab Software is a plus.
Work Environment

The successful candidate will work in a laboratory environment with moderate temperatures, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents.


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