Analytical Chemistry Supervisor- 2nd Shift

Initial Therapeutics, Inc.

Houston (TX)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Job summary

Initial Therapeutics, Inc. is looking for a Supervisor of Analytical Chemistry (2nd Shift) to oversee testing activities for raw materials and finished products. This role requires strong leadership in ensuring compliance with cGMP and quality control standards while managing team operations and resources. Candidates should possess a degree in Analytical Chemistry or a related field, along with 3-4 years of applicable experience in the pharmaceutical sector. Expertise in analytical instrumentation and regulations is essential for maintaining high-quality laboratory practices.

Qualifications

  • 3-4 years of experience in an analytical chemistry laboratory within the pharmaceutical industry.
  • Hands-on experience with wet chemistry analysis.
  • Familiarity with compliance regulations in an analytical setting.

Responsibilities

  • Oversee analytical testing of raw materials and finished products.
  • Review and interpret test results for accuracy and compliance.
  • Supervise maintenance and calibration of analytical equipment.
  • Ensure compliance with cGMP and data integrity requirements.
  • Lead the development and revision of SOPs.

Skills

Sample preparative chemistry
Wet chemistry analysis
Instrumental analysis procedures
Knowledge of quality control systems
Computer applications related to laboratory

Education

Bachelor's degree in Analytical Chemistry or related field

Tools

HPLC
GC
FTIR
UV-Vis Spectrophotometer
TOC analyzer
Wet Chemistry testing equipment

Job description

What We're Looking For

The Supervisor, Analytical Chemistry (2nd Shift) is responsible for providing scientific, logistical, and personal leadership within the analytical chemistry team focused on raw material, finished product, and stability testing. This individual will leverage their expertise to ensure the quality and efficiency of all analyses, drive continuous improvement, and expand the laboratory’s capabilities in support of pharmaceutical testing and compliance requirements. This role requires effective management of laboratory operations, personnel, and resources specific to the evening schedule, ensuring seamless transition and communication between shifts.

What You Will Do
  • Oversee, schedule and perform routine and non‑routine analytical testing of raw material, finished product, and stability 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, finished product, and stability 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, finished product, and stability analysis.
  • Keeps current with advances in analytical techniques, instrumentation, and regulatory expectations for raw material, finished product, and stability testing, with an emphasis on pharmaceutical industry standards.
  • Provides leadership and support across all raw material, finished product, and stability testing workstations, facilitating cross‑training and backup coverage as needed to ensure uninterrupted laboratory operations.
  • Ensures meticulous and compliant documentation of all 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, finished product, and stability 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.
Who We Are

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond‑use dating (BUD) determination and active ingredient potency. State‑of‑the‑art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com.

Qualifications & Skills (Preferred)
  • Good Judgement – Expert
  • Deductive Reasoning – Advanced
  • Detail Oriented – Expert
  • Analytical Instrumentation – Advanced
  • Active Listening – Expert
Behaviors (Preferred)
  • Thought Provoking: Capable of making others think deeply on a subject.
  • Innovative: Consistently introduces new ideas and demonstrates original thinking.
  • Team Player: Works well as a member of a group.
  • Leader: Inspires teammates to follow them.
Motivations (Preferred)
  • Ability to Make an Impact: Inspired to perform well by the ability to contribute to the success of a project or the organization.
  • Flexibility: Inspired to perform well when granted the ability to set your own schedule and goals.
  • Goal Completion: Inspired to perform well by the completion of tasks.
  • Self‑Starter: Inspired to perform without outside help.
Education Required

Bachelors or better in Analytical Chemistry or related field.

Experience

Experience required.

Licenses & Certifications (Preferred)

Certification in HPLC.

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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