Analysis Skills, Analytical Chemistry, Biotech and Pharmaceutical, Chemistry, Cleanroom, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Data Management, Documentation, Environmental Sciences, Establish Priorities, FDA (Food and Drug Administration), Food Science, Gas Chromatography, High Performance Liquid Chromatography (HPLC), Instrumentation, Interpersonal Skills, Laboratory Testing, Microsoft Office, Presentation/Verbal Skills, Quality Control, Regulatory Compliance, Safety/Work Safety, Standard Operating Procedures (SOP), Standards Development, Team Building, Test Lab, Testing, Time Management, Titration, Veritas Product Family
- Business Title: Analytical Chemist
Position Title: Analytical Chemist
Division: Bureau Veritas Consumer Products Services
Entity: Advanced Testing Laboratory Inc
Location: Iowa City, Iowa
Reports to: Site Manager
FLSA: Non-exempt
Hours Worked: Typically, a 12-hour rotating day/night shift (2-2-3), working every other weekend.
However, must be flexible to meet the needs of the department and complete other projects as assigned.
Position Summary:
The Analytical Chemist is responsible for performing complex laboratory testing to identify, quantify, and analyze the chemical components of samples, ensuring safety, quality, and regulatory compliance across various industries including pharmaceuticals, food, and environmental science.
Duties and Responsibilities:
It is everyone's responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress.
- Perform various sample preparation, extraction, and analysis techniques utilizing analytical methods.
- Perform serial dilutions to create standards and quality control samples following a written method.
- Perform identification, gravimetric, qualitative, and physical testing on a routine basis.
- Execute titration testing, chromatography (GC and/or HPLC), and atomic absorption (AA).
- Utilize basic instrumentation to perform testing on a routine basis.
- Meet all testing assignment deadlines and document all analysis in a timely and accurate manner.
- Perform method validations and verifications.
- Complete DIR/OOS/CAPA documentation.
- Assess SOPs and methods, recommend and initiate changes as needed.
- Support audit activities.
- Perform routine lab maintenance, maintaining a clean and safe laboratory space.
- Handle other essential tasks and responsibilities as assigned.
Skills & Proficiencies:
- Strong interpersonal skills such as relationship building, initiative, positive attitude, and team building.
- Ability to present facts and recommendations effectively, both written and verbal.
- Ability to manage time and prioritize work effectively.
- Ability to work independently as well as in a team environment.
- Accurate data management, sorting, and interpreting.
- Ability to work in a fast-paced, agile environment.
- Proficient in the Microsoft Office suite.
Education and Experience:
- Bachelor's Degree in Chemistry or a closely related scientific discipline.
- 0-1 years of experience working with GC, HPLC, or Atomic Absorption (AA) preferred.
- Experience in an FDA or cGMP regulated environment preferred.
An equivalent combination of education and experience may be accepted in lieu of above.
Compensation Range:
$22 - $24 an hour (e.g., the job posting is not necessarily reflective of actual compensation that may be earned, and actual compensation is subject to variation due to such factors as locations, education, experience, and skillset).