Analytical Chemistry Supervisor- Raw Material

Eagle

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's or Doctorate in Analytical Chemistry or related field
  • 3-4 years of experience in an analytical chemistry lab in the pharmaceutical industry
  • Hands-on experience with sample preparative chemistry and wet chemistry analysis
  • Understanding of instrumental analysis procedures in modern chemistry labs
  • Competency with laboratory-related computer applications
  • Knowledge of sampling methods and quality control systems

Responsibilities

  • Oversee and schedule analytical testing of raw materials according to procedures and regulatory guidelines
  • Review and interpret test results; lead investigations into unexpected outcomes
  • Supervise the maintenance and calibration of analytical equipment
  • Ensure team proficiency with relevant equipment and standard operating procedures
  • Stay updated on advances in analytical techniques and regulatory expectations
  • Provide leadership across testing workstations, facilitating cross-training
  • Ensure compliant documentation of testing activities and results
  • Lead the development and review of relevant SOPs and lab documentation

Benefits

  • Opportunity to lead and develop a team within a specialized field
  • Engagement with cutting-edge analytical techniques and instrumentation
  • Contribution to pharmaceutical manufacturing quality and compliance
  • Focus on continuous improvement of laboratory capabilities
  • Support for professional development and staying current with industry standards
Full Job Description
What We're Looking For

The Supervisor, Analytical Chemistry: Raw Material Testing is responsible for providing scientific, logistical, and personal leadership within the analytical chemistry team focused on raw material testing. This individual will leverage their expertise to ensure the quality and efficiency of all raw material analyses, drive continuous improvement, and expand the laboratory's capabilities in support of pharmaceutical manufacturing and compliance requirements.

What You Will Do
  • Oversee, schedule and perform routine and non-routine analytical testing of raw material samples according to established procedures and regulatory guidelines; ensures testing is completed within required timelines.
  • Reviews and interprets test results for accuracy and compliance; promptly notifies management of any unexpected or out-of-specification results and leads investigations and troubleshooting with minimal supervision.
  • Supervises the maintenance, calibration, and troubleshooting of analytical equipment (e.g., HPLC, GC, FTIR, UV-Vis Spectrophotometer, TOC analyzer, Wet Chemistry testing equipment) used for raw material testing to ensure all instruments are operating within calibration and performance standards; coordinates repair and preventive maintenance activities as needed.
  • Ensures team members maintain proficiency with all relevant equipment, systems, and standard operating procedures (SOPs) specific to raw material analysis.
  • Keeps current with advances in analytical techniques, instrumentation, and regulatory expectations for raw material testing, with an emphasis on pharmaceutical industry standards.
  • Provides leadership and support across all raw material testing workstations, facilitating cross-training and backup coverage as needed to ensure uninterrupted laboratory operations.
  • Ensures meticulous and compliant documentation of all raw material testing activities, results, and investigations in accordance with cGMP and data integrity requirements.
  • Leads the development, revision, and review of SOPs and laboratory documentation specific to raw material testing, ensuring timely updates to align with regulatory and operational changes.

Who You Are
  • Bachelor's, Master's or Doctorate degree in Analytical Chemistry or related science field, with directly related experience of 3-4 years in an analytical chemistry laboratory within pharmaceutical industry
  • Hands-on experience with sample preparative chemistry and wet chemistry analysis per compendial monograph procedures
  • Understanding of instrumental analysis procedures utilized in a modern chemistry laboratory
  • Demonstrated competence with computer applications and programs related to laboratory applications
  • Knowledge of sampling methods and quality control systems.

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