Advanced Research Associate - Aseptic Processing

Posted Yesterday
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St Paul, MN, USA
In-Office
50K-82K Annually
Mid level
Biotech
The Role
Support development and manufacture of reagents and consumables by authoring and executing SOPs, performing controlled experiments and equipment validation, investigating non-conformances, implementing process improvements, maintaining GMP/GDP documentation, training staff, and collaborating cross-functionally to meet quality and regulatory requirements.
Summary Generated by Built In

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 supports the development and sustained manufacture of Bio-Techne’s diverse product portfolio. This role involves executing and revising standard operating procedures, facilitating controlled experiments, and collaborating cross-functionally to advance new and existing products. The position implements process improvements, ensures compliance with quality standards, and supports operational excellence within a fast-paced environment.

Pay Range (Based on Experience Level):

$49,700-$71,000

Key Responsibilities: 

  • Author, revise, and execute Standard Operating Procedures (SOPs) for manufacturing reagents and consumables.
  • Facilitate moderately complex controlled experiments to support new product development.
  • Perform validation activities for equipment used in GMP manufacturing processes.
  • Follow Good Documentation Practices (GDP) to capture results, analyze generated data, and prepare comprehensive reports.
  • Perform timely reviews of in-process manufacturing documentation.
  • Identify and resolve observed manufacturing process issues.
  • Investigate and author non-conformance reports; lead troubleshooting activities.
  • Propose process improvement initiatives and lead implementation efforts.
  • Conduct periodic workspace walkthroughs, close out actions, and perform device calibrations to maintain compliance.
  • Collaborate with cross-functional teams to achieve project objectives.
  • Perform training for new employees and contribute to team development.
  • Follow company guidelines and comply with all safety, quality, and regulatory requirements.
  • Perform additional duties as assigned.

QUALIFICATIONS

Education and Experience:

  • Bachelor’s degree with 3–5 years of relevant experience, or
  • Master’s degree in a related field with up to 2 years of relevant experience.
  • GMP laboratory experience required.

Knowledge, Skills, and Abilities:

  • Knowledge of GMP and Good Documentation Practices (GDP) required.
  • Strong technical knowledge of aseptic filling.
  • Exposure to media fills and aseptic process qualification.
  • Ability to work in laminar flow hoods and RABS.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Ability to perform moderately complex data analysis.
  • Strong organizational skills and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to perform moderate complex calculations.
  • Effective verbal and written communication skills.
  • Ability to conduct training effectively.
  • Ability to multitask and prioritize effectively.

Working Conditions:

  • Onsite work required during standard business hours.
  • Occasional extended hours may be necessary to meet project deadlines.

Physical Requirements:

  • Ability to stand or sit for extended periods.
  • Ability to wear PPE and clean room attire.
  • Manual dexterity for handling laboratory equipment.
  • Ability to lift up to 25 lbs 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 [email protected] for assistance.

Skills Required

  • Bachelor's degree with 3-5 years relevant experience or Master's degree with up to 2 years relevant experience
  • GMP laboratory experience
  • Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Strong technical knowledge of aseptic filling and aseptic process qualification
  • Exposure to media fills
  • Ability to work in laminar flow hoods and Restricted Access Barrier Systems (RABS)
  • Experience performing equipment validation in GMP manufacturing processes
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Ability to perform moderately complex data analysis and calculations
  • Strong organizational skills, attention to detail, multitasking and prioritization ability
  • Effective verbal and written communication and ability to conduct training
  • Onsite work during standard business hours (ability to work onsite)
  • Physical ability to stand or sit for extended periods, wear PPE/clean room attire, manual dexterity, lift up to 25 lbs

Bio-Techne Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Bio-Techne and has not been reviewed or approved by Bio-Techne.

  • Healthcare Strength Medical and dental coverage are often regarded as strong, with core health benefits broadly available across U.S. roles. Day-one eligibility and comprehensive options are described as a relative bright spot even when pay sentiment is mixed.
  • Leave & Time Off Breadth PTO, paid holidays, paid parental leave, and volunteer time are emphasized alongside flexible scheduling. Work-life balance elements are seen as strengths relative to base-pay concerns.
  • Strong & Reliable Incentives Quarterly or semi-annual bonuses and eligibility for annual cash incentives add meaningful upside for many salaried roles. Structured plans such as a Management Incentive Plan reinforce predictability of variable pay.

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The Company
HQ: Minneapolis, MN
2,512 Employees
Year Founded: 1981

What We Do

Bio-Techne Corporation (NASDAQ: TECH) is a leading developer and manufacturer of high-quality purified proteins and reagent solutions - notably cytokines and growth factors, antibodies, immunoassays, biologically active small molecule compounds, tissue culture reagents, and cell and gene therapy workflow solutions including T-Cell activation technologies. Bio-Techne’s portfolio also includes protein analysis solutions, sold under the ProteinSimple brand name, that offer researchers efficient and streamlined options for automated Western blot and multiplexed ELISA workflow. These reagent and protein analysis solutions are sold to biomedical researchers, as well as clinical research laboratories, and constitute the Protein Sciences Segment. Bio-Techne also develops and manufactures diagnostic products including FDA-regulated controls, calibrators, blood gas and clinical chemistry controls, and other reagents for OEM and clinical customers. Bio-Techne’s genomic tools include advanced tissue-based in situ hybridization assays (ISH) for research and clinical use, sold under the ACD brand, as well as a portfolio of clinical molecular diagnostic oncology assays including the ExoDx®Prostate (IntelliScore) test (EPI) for prostate cancer diagnosis. These diagnostic and genomic products comprise Bio-Techne’s Diagnostics and Genomics Segment. Bio-Techne products are integral components of scientific investigations into biological processes and molecular diagnostics, revealing the nature, diagnosis, etiology and progression of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. With thousands of products in its portfolio, Bio-Techne generated approximately $714 million in net sales in fiscal 2019 and has over 2,200 employees worldwide.

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