Analytical Chemistry Supervisor (2nd Shift)

Location: Houston, Texas, United States; onsite, 2nd shift

Company

hirify.global provides cGMP testing, calibration, sterility, microbial detection, beyond-use dating, and active ingredient potency services for pharmaceutical and healthcare organizations.

What you will do

• Supervise, schedule, and perform routine and non-routine testing of raw materials, finished products, and stability samples.
• Review and interpret test results, report unexpected or out-of-specification results, and lead investigations and troubleshooting.
• Oversee maintenance, calibration, troubleshooting, repair, and preventive maintenance for HPLC, GC, FTIR, UV-Vis, TOC, and wet chemistry equipment.
• Develop team proficiency through training, cross-training, and backup coverage across laboratory workstations.
• Maintain compliant testing records and investigations in accordance with cGMP and data integrity requirements.
• Lead the development, revision, and review of SOPs and laboratory documentation.

Requirements

• Bachelor’s, master’s, or doctorate degree in Analytical Chemistry or a related science field.
• 3–4 years of directly related experience in an analytical chemistry laboratory within the pharmaceutical industry.
• Hands-on experience with sample preparation chemistry and wet chemistry analysis using compendial monograph procedures.
• Understanding of instrumental analysis procedures in a modern chemistry laboratory.
• Computer proficiency with laboratory applications, plus knowledge of sampling methods and quality control systems.

Culture & Benefits

• Work within an FDA-registered cGMP testing and calibration laboratory.
• Use state-of-the-art instrumentation and advanced scientific methodologies.
• Contribute to patient safety, regulatory compliance, and science-based healthcare solutions.
• Collaborate with pharmaceutical manufacturers, compounding facilities, hospitals, and clinical research organizations.