About this role
Meets all quality and productivity metrics and demonstrates strong teamwork and collaborationReviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies.Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.)Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs.Keeps supervisor informed of significant issues or developments identified during quality assurance activities.Learn new tasks and remember the processes associated with this role.Ability to communicate with Scientific staff for resolving commentsAbility to complete tasks in situations that have a speed or productivity quota.Communicates effectively with client staff membersConducts all activities in a safe and efficient mannerPerforms other duties as assigned Bachelor's degree is required. A degree in a relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical science, or other directly related field or degree with comparable coursework is preferred.Authorization to work in the United States indefinitely without restriction or sponsorship. Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply.
Excellent full time benefits including
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.