Role Summary
The Chemist I will perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Location: Boca Raton, Florida.
Responsibilities
- Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOPs).
- Perform instrument calibration or qualification according to written procedures.
- Perform testing as needed to generate data for method validations and other special projects, following general instructions on routine work and detailed instructions on new assignments.
- Fulfill requests from management for assistance in other matters as needed.
- Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines.
- Utilize cGMP practices in documentation and execution of job functions.
- Review documentation on trained tasks as assigned by manager.
Qualifications
- Required: Experience in a laboratory setting.
- Preferred: Work experience in a regulated environment (FDA, EPA, etc.) is preferred.
- Required: Ability to follow cGMPs and procedures with great attention to detail.
- Required: Ability to work in a high-pressure, deadline-driven environment.
- Required: Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines.
- Required: Time management skills and be able to balance multiple job assignments at once.
- Required: Excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations.
Education
- Required: B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline.