Quality Control Sr. Technician

Location: West Jefferson

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.

Responsibilities

• 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.

Key Qualifications

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.

Additional Requirements (May Be Requested in the Future)

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

Preferred Qualifications

The following qualifications are desired but not required:

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

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Benefits:
Live an Extraordinary Life
We care about your well-being, not just on the job. Battelle offers comprehensive and competitive benefits to help you live your best life.

• Balance life through a compressed work schedule
  :
  Most of our team follows a flexible, compressed work schedule that allows for every other Friday off-giving you a dedicated day to accomplish things in your personal life without using vacation time.
• Enjoy enhanced work flexibility, including a hybrid arrangement: You have options for where and when you work. Our Together with Flexibility model allows you to work 60% in-office and 40% remote, with Monday and Tuesday as common in-office days, dependent on team and position needs .
• Take time to recharge
  :
  You get paid time off to support work-life balance and keep motivated.
• Prioritize wellness
  :
  Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits.
• Better together
  :
  Coverage for…