Noblesville $24 - $28/HR Contract
Run a range of routine and advanced analytical tests using chromatography, spectroscopy, titration, and similar scientific tools.
Perform assessments on raw inputs, mid-process samples, and completed batches based on established procedures and controlled-environment guidelines.
Evaluate results, interpret data trends, and produce accurate and well-organized documentation.
Keep lab instruments functioning properly through routine calibration, qualification tasks, and basic troubleshooting.
Contribute to method-related activities, including development, validation, and stability testing efforts.
Follow all internal quality requirements and external regulatory frameworks that apply to regulated production environments.
Assist with investigations into unexpected results or process deviations and help identify causes and corrective measures.
Maintain an orderly and safe laboratory work area while consistently following safety practices.
Support internal and external audits, regulatory inspections, and documentation requests.
Uphold compliance with both U.S. and international quality and regulatory bodies (e.g., federal agencies, global health authorities, and relevant standards organizations).
Bachelor’s degree in a science discipline such as chemistry, biology, or a related field.
Minimum of two years of hands-on experience in analytical testing or laboratory operations.
Working knowledge of key analytical instruments (chromatography systems, spectroscopic tools, etc.).
Familiarity with quality systems and regulatory expectations used in controlled manufacturing environments.
Strong problem-solving ability, including evaluating issues under pressure and supporting root-cause investigations.
Demonstrated understanding of regulated-industry quality practices, particularly those used in pharmaceutical manufacturing.
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