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:
$73,100.00 - $120,200.00By 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.
Position Overview
The Tech Transfer Engineer is responsible for transforming internally developed diagnostic products into fully defined, manufacturable, and compliant production processes. This role focuses heavily on operations, ensuring that all procedures, batch records, and work instructions are clearly written, validated, and ready for seamless execution on the manufacturing floor. Working closely with R&D, Manufacturing, Quality, and Program Management, this person ensures that IVD calibrators, controls, and diagnostic assays move smoothly from development through production and ultimately to customer release.
Key Responsibilities
Operationalization of Development Outputs
- Translate R&D development work into clear, detailed, and compliant work instructions, batch records, formulation instructions, and work instructions.
- Ensure all operational documentation reflects customer product design requirements, performance specifications, and regulatory constraints.
- Identify manufacturability gaps early and collaborate with R&D to refine processes for operational efficiency and robustness.
Technology Transfer to Manufacturing
- Lead the tech transfer process of new products and processes from development into manufacturing.
- Develop comprehensive tech transfer packages including process flows, equipment needs, critical parameters, and quality controls.
- Support training of manufacturing personnel on new SOPs, workflows, and product-specific handling requirements.
- Support engineering runs, pilot lots, OQ/PQ and initial production batches to confirm documentation accuracy and process readiness.
Process Definition & Standardization
- Create standardized templates and documentation frameworks to streamline future tech transfers.
- Define critical process parameters, in-process controls, and acceptance criteria in collaboration with R&D and Quality.
- Ensure all operational documents are optimized for clarity, usability, and compliance.
Cross-Functional Collaboration
- Serve as the operational bridge between R&D, Manufacturing, Quality Assurance, Quality Control, and Program Management.
- Participate in customer meetings to clarify design intent, operational constraints, and documentation expectations.
- Provide input on project timelines, resource planning, and manufacturability considerations.
Compliance & Documentation Control
- Author and revise work instructions, batch records, and technical reports in compliance with GMP and ISO standards.
- Support internal and external audits on tech transfer by providing accurate, up-to-date operational documentation.
- Maintain document control discipline, ensuring revisions, approvals, and change controls are properly executed.
Continuous Improvement
- Identify opportunities to improve process clarity, reduce variability, and enhance operational efficiency.
- Drive updates to tech transfer SOPs and new product batch records based on production feedback, deviations, and CAPA outcomes.\
- Contribute to the development of best practices for documentation, tech transfer, and operational readiness.
Qualifications
Education & Experience
- Bachelor’s degree in Biochemistry, Molecular Biology, Chemistry, Biomedical Engineering, or related field.
- 3–7 years of experience in diagnostics, IVD manufacturing, or biotech operations.
- Experience writing SOPs, batch records, or technical manufacturing documentation is strongly preferred.
- Background in IVD assay development, reagent formulation, or calibrator/control production is a plus.
Technical Skills
- Strong understanding of IVD manufacturing processes, including reagent preparation, filling, lyophilization (if applicable), labeling, and packaging.
- Experience with statistical tools for assessing process capability and quality control.
- Familiarity with ISO 13485, GMP/QSR, design control, and risk management (ISO 14971).
- Ability to interpret development data, customer requirements, and assay performance characteristics to define operational processes.
- Exceptional technical writing and documentation skills.
- Strong attention to detail and commitment to accuracy.
- Effective communicator who can collaborate across R&D and operations.
- Organized, proactive, and comfortable managing multiple projects in parallel.
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.
Top Skills
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.
