As an Associate Material Validation Specialist, your primary responsibility will be to perform scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods, ensuring compliance with established standards. You will conduct and validate biological and chemical QC assays, compile and interpret statistical data, and prepare qualification plans and reports to support material acceptance decisions. In addition, you will participate in audits and inspections, develop and maintain standard operating procedures, and contribute to the effectiveness of our Quality Management System in alignment with ISO, FDA, and other regulatory requirements.
To succeed in this role, you will have excellent organizational, time management, and communication skills. You will be detail-oriented, skilled at diagnostic test methods and interpreting results, and able to adapt in a project-driven work environment. Proficiency with Microsoft Office is required, and experience with automated clinical chemistry analyzers would be considered an asset. The ideal candidate will possess a Bachelor of Science degree or a related field of study and have a minimum of two years of practical laboratory experience. A combination of education and experience will be considered.
The anticipated base salary for this position is $54,500 - $68,000. This role may also qualify for annual incentives and/or comprehensive benefits. The actual base salary offered will depend on a variety of factors, including without limitation, the qualifications of the individual applicant for the position, years of relevant experience, level of education attained, certifications or other professional licenses held, and if applicable, the location of the position.
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