Analytical Chemist

Direct message the job poster from Bell International Laboratories

The Analytical Laboratory Chemist is pivotal in conducting and managing analytical testing of raw materials, in-process samples, and finished products to ensure compliance with cGMP standards. This role supports the Quality Control Lab Manager in upholding the integrity and quality of the laboratory environment.

• Develop and validate analytical methods to ensure reliability and accuracy of test results.
• Operate and maintain sophisticated laboratory instruments, including HPLC, GC, UV-Vis, and FTIR.
• Conduct routine calibration and validation of laboratory instruments to maintain compliance with operational standards.
• Prepare and analyze samples from raw materials, in-process batches, and finished products using both wet chemistry techniques and instrumental analysis.
• Maintain meticulous laboratory records and notebooks, ensuring detailed documentation following regulatory requirements.
• Collaborate with team members to efficiently complete testing assignments within set timelines.
• Monitor ongoing product quality to confirm adherence to established standards and specifications.
• Adhere to Standard Operating Procedures (SOPs) and global methodological standards such as USP, AOCS, and ASTM.
• Troubleshoot and perform minor repairs on analytical instruments to minimize downtime.
• Implement safety protocols for handling chemicals, managing laboratory waste, and maintaining a clean lab environment.
• Organize and manage laboratory inventory to ensure availability of necessary supplies and equipment.
• Mentor and train new laboratory personnel on testing procedures and instrument operations.

• Proficient in the use of standard laboratory equipment and familiar with advanced analytical techniques.
• Excellent communication skills, both verbal and written, with the ability to convey complex information clearly.
• Strong analytical thinking and problem‑solving capabilities.
• Effective time management skills to handle multiple tasks and meet strict deadlines.
• Demonstrated ability to work autonomously in a dynamic, fast‑paced environment.
• Keen attention to detail with a commitment to high‑quality work.
• Flexibility to adapt to new procedures or rapid changes in project priorities.
• Proficient in Microsoft Office.

• Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.
• 3 to 5 years of hands‑on experience in an analytical laboratory setting, preferably within the personal care, pharmaceutical, or related industries.
• Extensive knowledge of cGMP practices, organic chemistry, and instrumental analytics (HPLC, GC, UV‑Vis, FTIR).

Associate

Full‑time

Analyst, Science, and Quality Assurance

Industries:
Personal Care Product Manufacturing

• Medical insurance
• Vision insurance
• 401(k)
• Paid maternity leave
• Paid paternity leave
• Tuition assistance
• Disability insurance

St Paul Park, MN

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