Advanced Research Associate - Manufacturing

Bio-Techne Corp.; Austin, Northern (TX, KY); Hybrid; USD 50,000 - 82,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k

ESPP

HSA

FSA

Parental leave

Job summary

Bio-Techne Corp. in Austin, TX is seeking an Advanced Research Associate to support end-to-end production, focusing on formulation and quality control of reagents before finishing kits.

The role requires hands-on experience with molecular assays (PCR/CE, qPCR, NGS) and a strong attention to documentation and accuracy. Ideal candidates hold a Bachelor’s degree in a scientific field with 2–5+ years in manufacturing.

Qualifications

• Bachelor’s degree in a scientific discipline or equivalent.
• 2-5+ years of production experience.
• Experience setting up and analyzing molecular assays (PCR/CE, qPCR, NGS).
• Ability to work in a fast-paced manufacturing environment and follow GMP-like practices.

Responsibilities

• Follow manufacturing protocols to formulate reagents.
• Functionally test products and review data for specification compliance.
• Assist downstream production by filling, labeling and packaging reagents.
• Maintain accurate records and perform instrument maintenance.
• Support cross-functional teams on projects and contribute to process improvements.

Skills

Molecular assays

PCR/CE

qPCR

NGS

Office software

Database management

Attention to detail

Documentation

Education

Bachelor’s degree in a scientific discipline or equivalent

Tools

ERP systems

QAD

Job description

## Advanced Research Associate - ManufacturingApply: In-person: Austin, TX: Full time: Posted Yesterday: JR102189**By joining Bio-Techne, you’ll 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:$49,700.00 - $81,650.00**Position Summary** The Advanced Research Associate will have experience running and troubleshooting molecular assays, preferably in a manufacturing environment. This role will support end to end production with primary focus on the formulation and quality control of reagents prior to being processed into finished kits.**Key Responsibilities*** Follow manufacturing protocols to formulate reagents.* Functionally test products, reviewing data obtained for compliance to established specifications.* Propose solutions to technical issues with management or technical lead prior to executing.* Assist in downstream production by following work instructions to fill, label and package reagents.* Maintains quality of manufactured products; recording information accurately while following Good Documentation Practices as well as verifying work performed by co-workers.* Document non-conformances and deviations.* Follows work instructions to inspect, test and release raw materials.* Perform rework as required according to designated work instructions.* Coordinate and perform equipment maintenance.* Perform equipment validation as required.* Perform product stability testing according to work instructions.* Maintain accurate inventory through the timely and accurate completion of work order and inventory transactions and by performing weekly cycle counts.* Perform general lab maintenance, cleaning, and organization.* Execute work in a safe manner. Notifying management of any safety issues or risks and assisting in remediation of those safety issues or risks.* Apply experience and logic to resolve a variety of moderately complex problems.* Provide support for cross-functional teams on complex projects.* Identify and implement process improvements.* Revise and update procedures as needed.* Perform all other duties as assigned.**Knowledge, Skills, And Abilities*** Experienced in the setup and analysis of Molecular assays, PCR/CE, qPCR and NGS preferred.* Skilled in the use of software programs such as Microsoft Office and database management programs.* Organized, process-oriented individual with an attention to detail.* Good time management skills.* Ability to perform repetitive tasks with high degree of accuracy.* Good written and communication skills.* Able to work in a fast-paced environment.* Readily adaptable to changing demands.* Familiarity with ERP systems, QAD a plus.* Ability to work cohesively in a team environment.* Knowledge of lean manufacturing principals.* Knowledge of cGMP, GLP, ISO, CE or other regulated environments. **Education and Experience**Bachelor’s degree in a scientific discipline or equivalent and 2-5+ years’ experience in a production environment; or a combination of education and applicable work experience. **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.** ***This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). 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*** ***[e-mail]*** ***for assistance.***