Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
Reviews 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 comments
Ability to complete tasks in situations that have a speed or productivity quota.
Communicates effectively with client staff members
Conducts all activities in a safe and efficient manner
Performs other duties as assigned

Qualifications

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.

Additional Information

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 options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.