Advanced Research Associate – Viral Clearance

By joining Bio-Techne youll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne and all of its brands provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

Are you passionate about science and have a drive to apply yourself to understanding how manufacturing processes can impact product safety

As an Advanced Research Associate on the Viral Clearance team you will apply chromatography cell culture bioassays and molecular biology techniques to evaluate the impact of various purification conditions and processes on the inactivation and removal of model viruses from our products. Working in a BSL-2 laboratory environment you will assess viral clearance using model viruses and contribute to ensuring product safety. You will also support the development of new methods and prepare summary reports that document the effectiveness of manufacturing processes to clear viral loads in support of regulatory submissions for our GMP this role you will work with animal-derived model viruses in an environmentally controlled facility and will have the opportunity to contribute to process improvements while performing additional duties as assigned.

Pay Range: $42600 - $81650

Key Responsibilities:

• Develop and conduct moderately complex experiments and report test results in compliance with SOPs and GxP standards.
• Maintain accurate complete and audit-ready laboratory and product documentation including drafting and revising SOPs.
• Support projects and new product development.
• Prepare technical reports and clearly communicate findings to team members and key stakeholders.
• Participate in new method development and validations as well as cross-functional projects and team meetings.
• Perform troubleshooting investigations.
• Identify and implement continuous improvement opportunities to enhance testing quality and operational efficiency.
• Collaborate with Operations Process Engineering Quality Assurance (QA) Quality Control (QC) and Regulatory Affairs (RA) to ensure consistent and robust process performance.
• Perform laboratory support functions including instrument calibration and maintenance reagent preparation and ordering waste disposal and laboratory cleaning.
• Adhere to company policies and safety requirements including AWAIR Chemical Hygiene and Exposure Control guidelines.

Education and Experience:

• Bachelors degree in Biological Sciences or a related field with a minimum of 3-5 years of relevant laboratory experience or a Masters degree with up to 2 years of relevant laboratory experience.
• Industry experience including familiarity with GMP environments is preferred.
• Experience with viral clearance methodologies is preferred.

Knowledge Skills and Abilities:

• Knowledge of cell culture protein chemistry molecular biology and associated laboratory techniques with demonstrated hands-on proficiency.

• Understanding of quality systems and experience working in regulated environments (e.g. GMP ISO).
• Attention to detail organizational skills and demonstrated proficiency in data analysis and problem-solving.
• Critical-thinking skills with the ability to apply technical knowledge to troubleshooting and project execution.
• Ability to work effectively in a fast-paced environment manage multiple priorities and communicate clearly both verbally and in writing.
• Ability to produce accurate high-quality work and maintain thorough documentation.
• Experience developing reviewing and implementing standard operating procedures.
• Effective interpersonal communication skills including the ability to collaborate and present technical information clearly.
• Self-motivated learner with the ability to quickly acquire and apply new techniques using available resources.
• Ability to work independently on routine assignments and work with a team.
• Proficient in Microsoft Excel and standard Windows-based applications.
• Ability to handle sensitive and proprietary information with discretion.
• Commitment to safety and adherence to company policies and procedures.
• Ability to work hours that adhere to standard business operations (8:00 A.M. to 5:00 P.M.)
• Ability to meet project timelines and adapt to changing priorities including flexibility to work additional hours as needed.

Why Join Bio-Techne:

• We offer competitive insurance benefits starting on day one: medical dental vision life short-term disability long-term disability pet and legal and ID shield.
• We invest in our employees financial futures through 401k plans an employee stock purchase plan (ESPP) Health Saving Account (HSA) Flexible Spending Account (FSA) and Dependent Care FSA.
• We empower our employees develop their careers through mentorship promotional opportunities training and development tuition reimbursement internship programs and more.
• We offer employee resource groups volunteer paid time off employee events and charity drives to build a culture of caring and belonging.
• We offer an accrued leave policy with paid holidays paid time off and paid parental leave.
• We foster a culture of empowerment and innovation where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.

All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability or status as a protected veteran.

To protect the interests of all Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

If you require a reasonable accommodation to complete an application participate in an interview or take part in any other stage of the recruitment process please contact for assistance.