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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 with diverse backgrounds and experiences and welcome all qualified individuals to apply.

Job Summary

Battelle’s Biomedical Research Center is currently seeking an In-Vitro Assay Senior Technician specializing in virology. This position is located in West Jefferson, OH . This position will provide technical support performing standard and complex in-vitro assays to include, but not limited to PCR, ELISA, and cell-based assays as well as other in vitro-related activities. This position is Monday through Friday and will require frequent overtime on nights and weekends; schedule may include holidays.

Responsibilities

• Work projects may include but not limited to:

• Working with highly hazardous biological materials in Biological Safety Level 2 (BSL-2) and Biological Safety Level 3 (BSL-3) laboratory

• Performing standard microbiological procedures; perform standard viral assays such as plaque assay, hemagglutination assay, and plaque reduction neutralization assays

• Focus will be on viral cell-based assays and virus propagation

• Perform standard In Vitro Assays such as ELISA, PCR, RNA and DNA isolations, and Flow Cytometry

• Maintaining mammalian, viral, and bacterial cell cultures

• Contributing to the development and validation of equipment and biological assays

• Ability to write and execute study protocols, methods, and SOPs

• Ability to work independently and efficiently in a team environment

• Decontaminating equipment and materials

• Maintaining appropriate documentation

• Recognize when technical operations deviate from accepted practices.

• Read SOPs, methods, facility guidelines, etc. used in workplace in a timely manner and adhere to these procedures.

• Use proper technique to operate necessary equipment to produce high quality data. Operate routine computer programs and perform basic data manipulation in a spreadsheet environment. Set up, validate, and operate laboratory equipment and software. Ensure that all equipment used for studies is routinely maintained and/or calibrated.

• Perform experiments using ratios, percentages, linear regression algorithms, and other basic mathematical and scientific principles. Organize and interpret scientific data.

• Contribute to and/or write reports and data summaries and organize data tables.

• Conduct Quality Control and Technical reviews of study data as needed.

• Ensure that the proper solutions are prepared, that solutions and reagents are not beyond their expiration date, and that the proper paperwork is maintained. Be responsible for ordering reagents, supplies, and equipment. Organize, clean, and maintain the facility laboratories in accordance with GLP and ISO guidelines.

• Demonstrate knowledge and understanding of theory behind applications and ability to troubleshoot if needed.

• Maintain a good work attendance record and be punctual for all project work.

• Adhere to all laboratory safety requirements.

• Works on assignments that are moderately complex in nature where judgment is required in assessing problems and making recommendations.

• Performs non-routine analysis to verify the accuracy, applicability, and reasonableness of project work. May assist in identifying ways to control and/or reduce fixed costs without negatively impacting client expectations. May assist in the technical planning and has some discretion when making judgments and completing tasks. Is encouraged to make recommendations such as estimating time requirements for the completion of tasks and/or providing solutions to technical problems.

• Provides input to Project Manager on time and staff resources. Trains and guides less experienced staff on specific tasks. Provides input to performance reviews, as requested.

• Works under general supervision and instruction of more experienced staff. Reports observations/problems clearly and concisely, recognizing and highlighting specific deviations.

• Demonstrates the ability to perform assignments that may not be standardized in nature. Exhibits technical knowledge to perform moderately complex assignments. Demonstrates knowledge and understanding behind application by beginning to troubleshoot and interpret results. Conducts specified non-routine analysis of data and prepares data for written reports. Uses established outlines for documenting results for inclusion in technical reports.

Key Qualifications

• Associate’s degree in microbiology/molecular biology plus 3 years’ experience, or a Bachelor’s degree in microbiology/molecular biology plus 2 years’ experience.

• 2 years’ experience in a laboratory setting working with viruses post higher level graduation

• Experience growing viruses and/or experience developing viral assays

• Strong written and oral communication skills.

• Must be a US citizen.

• Ability to obtain/maintain certification in the Biological Suitability Assessment Program (BSAP).

• Ability to obtain/maintain DoJ Security Risk Assessment (SRA) approval.

• Ability to obtain/maintain CDC approval to work with BSAT material.

• Must be willing to work in a biosafety level 2 (BSL2) and 3 (BSL3) (biocontainment) environment and able to wear appropriate respiratory protection.

• Must be willing to be immunized with FDA licensed vaccines and Investigational New Drugs (IND) recommended for persons at risk to occupational exposure of biological agents.

• Must be willing to participate in random drug screening.

• Respond appropriately to various alarms and potential emergency situations.

• Sufficiently medically fit to do work in a lab wearing appropriate respiratory equipment and perform all assigned duties.

• Ability to work night, weekend, and holiday hours.

• Newly hired employees are subject to a 90-day Introductory Period, during which their performance is evaluated by supervision.

Preferred Qualifications

• Preference will be given to candidates with prior experience working in a BL-2 and/or BL-3 laboratory and those with knowledge or training in FDA Good Laboratory Practices (GLP)

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.

• 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 partners, gender-affirming care and health support, and family formation support.

• Build your financial future : Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that.

• Advance your education : Tuition assistance is available to pursue higher education.

• Flexible work arrangements : You have options for where you work and when you work.

A Work Environment Where You Succeed

For brilliant minds in science, technology, engineering and business operations, Battelle is the place to do the greatest good by solving humanity’s most pressing challenges and creating a safer, healthier and more secure world.

You will have the opportunity to thrive in a culture that inspires you to:

• Apply your talent to challenging and meaningful projects

• Receive select funding to pursue ideas in scientific and technological discovery

• Collaborate with world-class experts in an inclusive environment

• Nurture and develop the next generation of scientific leaders

• Give back to and improve our communities

Vaccinations & Safety Protocols

Battelle may require employees, based on job duties, work location, and/or its clients’ requirements to follow certain safety protocols and to be vaccinated against a variety of viruses, bacteria, and diseases as a condition of employment and continued employment and to provide documentation that they are fully vaccinated. If applicable, Battelle will provide reasonable accommodations based on a qualified disability or medical condition through the Americans with Disabilities Act or the Rehabilitation Act or for a sincerely held religious belief under Title VII of the Civil Rights Act of 1964 (and related state laws).

Battelle is an equal opportunity employer. We provide employment and opportunities for advancement, compensation, training, and growth according to individual merit, without regard to race, color, religion, sex (including pregnancy), national origin, sexual orientation, gender identity or expression, marital status, age, genetic information, disability, veteran-status veteran or military status, or any other characteristic protected under applicable Federal, state, or local law. Our goal is for each staff member to have the opportunity to grow to the limits of their abilities and to achieve personal and organizational objectives. We will support positive programs for equal treatment of all staff and full utilization of all qualified employees at all levels within Battelle.

The above statements are intended to describe the nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, activities and skills required of staff members. No statement herein is intended to imply any authorities to commit Battelle unless special written permission is granted by Battelle's Legal Department.

For more information about our other openings, please visit www.battelle.org/careers