Quality Control Sr. Technician

Overview

Battelle delivers when others can’t. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients—whether they are a multi-national corporation, a small start-up or a government agency.

We recognize and appreciate the value and contributions of individuals from a wide range of backgrounds and experiences and welcome all qualified individuals to apply.

Job Summary Battelle is currently seeking a Quality Control Senior Technician
. This position is located in West Jefferson, OH
.

Battelle’s Biomedical Research Center (BBRC) is seeking a well-organized, detail-oriented, and dependable team player to join our High Containment Bio group as a Quality Control (QC) Senior Technician. In this role, the incumbent will review data and reports for quality and collaborate across functional groups and with study management teams to deliver high-quality data, documents, and reports.

The QC Senior Technician must maintain and review data to ensure that all client, regulatory, organizational, ethical, and/or legal requirements are met. This role supports a deadline-driven environment, and we are seeking an individual who is accustomed to working within tight timelines while maintaining high-quality work.

This position is Monday through Friday and may require occasional overtime during evenings or weekends.

• Create and maintain study files in accordance with standard operating procedures, protocols, quality requirements, and client specifications.
• Perform timely quality control and/or technical review of electronic and/or paper data.
• Provide a variety of administrative support to a complex project or multiple projects.
• Prepare and submit study files for Quality Assurance (QA) audits.
• Coordinate corrective actions based on QA audit findings.
• Set up databases, analyze data from various databases, and create output that provides accurate information interpreted from the data.
• Generate output files, including layouts, formats, graphics, and tables.
• Prepare study files for archiving in accordance with standard operating procedures, regulatory requirements, and client specifications.
• Track and summarize QC metrics.
• Participate in QC continuous improvement initiatives.
• Perform other duties as assigned.

The following requirements must be met to be considered for this position:

• Associate degree in a related field, or an equivalent combination of education and experience in a related field. The candidate may be expected to pursue certifications or continuing education units, as needed.
• At least 3 years of applicable experience performing quality control review of laboratory animal, chemistry, and/or assay data and reports.
• Demonstrated attention to detail, ability to work independently, and ability to meet deadlines.
• Demonstrated knowledge of Microsoft Excel, Word, Access, and SharePoint.
• Demonstrated communication skills and proficiency in English language and grammar.
• Working knowledge of Good Laboratory Practices (GLP) in support of clinical or non-clinical studies.
• Must be a U.S. Citizen to perform the duties of this role.
• Must be willing to work in a Biosafety Level 2 (BSL-2) and/or Biosafety Level 3 (BSL-3) environment and able to wear appropriate respiratory protection.
• Must be willing to be immunized with licensed and FDA-approved vaccines and medications recommended for individuals at risk of occupational exposure to biological agents.
• Must be willing to participate in periodic drug screening.
• Newly hired employees are subject to a 90-day introductory period, during which performance is evaluated by supervision.

• Ability to obtain and maintain Department of Justice (DOJ) Security Risk Assessment (SRA) approval.
• Ability to obtain and maintain CDC Select Agent Program approval.

The following qualifications are desired but not required
:

• Bachelor’s degree.
• Working knowledge of Provantis.

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