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Associate Technology Transfer Jobs in New York (NOW HIRING)

AMRESCO

Senior Scientist

Bridgewater, NJ · On-site

$93K - $127K/yr

... up, technology transfer, or GMP manufacturing support. * Familiarity with high-throughput ... Join our global team of 14,000+ associates whose passion for discovery and determination to ...

Avantor Inc.

Senior Scientist

Bridgewater, NJ · On-site

$93K - $127K/yr

... up, technology transfer, or GMP manufacturing support. * Familiarity with high-throughput ... Join our global team of 14,000+ associates whose passion for discovery and determination to ...

Pioneer Data

Lab Technician / Pharma Industry

Pearl River, NY · On-site

$19.50 - $26/hr

As an associate, your focus on the job will contribute in achieving project tasks and goals ... technology transfer, and start-up activities. Applies established analytical tools to reduce cycle ...

Keylent Inc

ETL Developer / AbInitio

Manhattan, NY · On-site

$56.25 - $73.50/hr

... team as a Business Associate. This role involves leading the design and implementation of ... Information Technology, or a related field • Ability to manage multiple tasks and projects ...

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All JobsAssociate Technology Transfer JobsAssociate Technology Transfer Jobs in New York

Associate Technology Transfer information

What is an associate technology transfer?

Associate Technology Transfer professionals assist in the process of moving scientific discoveries or innovations from research settings into commercial or practical applications. They typically help with activities such as evaluating inventions, managing intellectual property, and facilitating licensing agreements between research institutions and external partners. Their work supports the commercialization of new technologies, often bridging the gap between researchers and industry. They also help ensure compliance with legal and regulatory requirements related to technology transfer.

What are the key skills and qualifications needed to thrive as an associate technology transfer?

To thrive as an Associate Technology Transfer, you need a solid background in life sciences or engineering, often supported by a bachelor’s or master’s degree in a related field. Familiarity with regulatory documentation, laboratory information management systems (LIMS), and technology transfer protocols is typically required. Strong project management, attention to detail, and effective cross-functional communication are essential soft skills for this role. These skills ensure smooth process transfers, regulatory compliance, and successful collaboration between research, development, and manufacturing teams.

What are some common challenges faced by associate technology transfer professionals during the handover of new processes from R&D to manufacturing?

Associate Technology Transfer professionals often encounter challenges such as aligning technical documentation, resolving discrepancies between lab-scale and production-scale results, and managing tight timelines to meet project milestones. Communication is key, as they must collaborate closely with R&D, quality assurance, and manufacturing teams to ensure all process parameters are clearly understood and reproducible. Navigating regulatory requirements and troubleshooting unexpected process deviations are also frequent aspects of the role, requiring strong problem-solving skills and attention to detail.

What is the difference between Associate Technology Transfer vs Technology Licensing Associate?

AspectAssociate Technology TransferTechnology Licensing Associate
Required CredentialsBachelor's degree, knowledge of patent processes, and industry regulationsBachelor's degree, understanding of licensing agreements, and industry standards
Work EnvironmentResearch institutions, universities, biotech, and pharma companiesLegal departments, corporate offices, biotech, and pharma firms
Employer & Industry UsageCommonly employed in research-heavy organizations managing technology transferOften found in legal or licensing departments handling patent licensing
Comparison Search IntentUnderstanding roles in technology transfer processesDistinguishing licensing responsibilities from transfer activities

Associate Technology Transfer and Technology Licensing Associate roles often overlap but focus on different aspects of managing intellectual property. The former primarily handles the transfer of technology from research to commercialization, while the latter concentrates on licensing agreements and legal negotiations. Both roles require knowledge of patents and industry regulations but serve distinct functions within the innovation ecosystem.

What are the most commonly searched types of Technology Transfer jobs in New York?

The most popular types of Technology Transfer jobs in New York are:

What are popular job titles related to Associate Technology Transfer jobs in New York?

For Associate Technology Transfer jobs in New York, the most frequently searched job titles are:

What job categories do people searching Associate Technology Transfer jobs in New York look for?

The top searched job categories for Associate Technology Transfer jobs in New York are:

What cities in New York are hiring for Associate Technology Transfer jobs?

Cities in New York with the most Associate Technology Transfer job openings:

Associate Technology Transfer jobs near you

Senior Scientist - Process Development

Avantor Fluid Handling, LLC

Bridgewater, NJ • On-site

$93K - $127K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

Job description

The Opportunity:Under limited supervision, develop and implement solutions for customers based on our products and services through close collaboration with customers and other innovation associates/scientists. Identify and develop innovative applications for a range of products to solve specific customer issues by planning and executing hands on studies at internal and customer laboratories.

WhatWe'reLooking For

  • Ph.D. in Molecular Biology, Biochemistry, Bioengineering, Chemical/Biochemical Engineering, Pharmaceutical Sciences, Biotechnology, ora related field(required).

  • Minimum of 5+ years of relevant industry experience in mRNA, RNA, nucleic acid, biologics, or pharmaceutical process development. Doctoral or relevant academic experience may be considered equivalent to industry experience.

  • Strong understanding of mRNA process development, including DNA template generation, in vitro transcription (IVT), enzymatic processing, purification, and analytical characterization.

  • Hands-on experience with nucleic acid process development, molecular biology techniques, and scalable manufacturing processes.

  • Knowledge of process development principles including DOE,QbD, process characterization, scale-up, risk assessment, and CPP/CQA relationships.

  • Experience troubleshooting complex technical challenges, interpreting multidisciplinary data, and developing data-driven solutions.

  • Excellent technical writing, presentation, project leadership, and cross-functional communication skills.

Preferred Qualifications

  • End-to-end mRNA development experience from DNA template preparation through purified mRNA and formulation interface.

  • Experience with IVT, capping/polyadenylation, chromatography, TFF/UF-DF, process scale-up, technology transfer, or GMP manufacturing support.

  • Familiarity with high-throughput automation, continuous manufacturing, process intensification, PAT, or advanced manufacturing technologies.

  • Experience with mRNA analytical techniques such as HPLC/UPLC, LC-MS, CE, qPCR/ddPCR, Bioanalyzer/TapeStation, sequencing, or impurity analysis.

  • Experience applying DOE,QbD, JMP, Minitab, Python, R, or related statistical and data-analysis tools.

  • Exposure to GMP/GLP environments, regulatory documentation, method qualification, validation, or technology transfer activities.

  • Experience evaluating emerging technologies, vendors, CDMOs, external collaborations, or technical due diligence opportunities.

How You Will Thrive and Create an Impact

Process Development

  • Design, develop, andoptimizeend-to-end mRNA manufacturing processes, including DNA template generation, IVT, enzymatic processing, purification, buffer exchange, and formulation interfaces.

  • Develop robust and scalable workflows to improve mRNA yield, purity, quality, process robustness, and manufacturability.

  • Apply DOE,QbD, risk assessment, and statistical tools to build process understanding andestablishrelationships between process parameters and product quality attributes.

  • Collaborate with Analytical Development to characterize mRNA identity, integrity, purity, potency-related attributes, and process impurities.

  • Troubleshoot process and product-quality challenges using scientific and data-driven approaches, including root cause analysis and risk mitigation.

  • Author technical reports, development summaries, risk assessments, SOPs, study protocols, andregulatory-supportdocumentation.

  • Evaluate anddemonstrateemerging technologies including synthetic DNA, novel purification approaches, automation, process intensification, and continuous manufacturing concepts.

Development Support

  • Support process characterization, control strategy development, and implementation of CPPs, CQAs, in-process controls, and processmonitoringstrategies.

  • Collaborate with manufacturing, quality, analytical, formulation, and regulatory teams to ensure successful process transfer and commercial readiness.

  • Participate in deviation investigations, change controls, root cause analyses, and continuous improvement initiatives.

  • Support GMP documentation activities including batch records, SOPs, process transfer packages, and validation-related documentation.

  • Assess external technologies, vendors, CDMOs, and strategic collaboration opportunities through proof-of-concept studies, technical due diligence, and workflow integration assessments.

  • Present technical findings, recommendations, and development strategies to project teams, cross-functional stakeholders, and senior leadership.

  • Mentor junior scientists and contribute to a culture of scientific excellence, innovation, safety, and operational rigor.

Disclaimer:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

Pay Transparency:

The expected pre-tax pay for this position is

$107,500.00 - $173,075.00

Actual pay may differ depending on relevant factors such as prior experience and geographic location.

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.comand let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

For more information about equal employment opportunity protections, please view the Know Your Rights poster.

Privacy Policy:

We will use the personal information that you have submitted to us in order to consider your application for the relevant role.

Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.

3rd Party Non-Solicitation Policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

Avantor offers a comprehensive benefits package including medical, dental, and vision coverage, wellness programs, health savings and flexible spending accounts, a 401(k) plan with company match, and an employee stock purchase program. Employees also receive 11 paid holidays, accrue 18 PTO days annually, are eligible for volunteer time off and 6 weeks of 100% paid parental leave (except in states that offer paid family leave). These benefits may not apply to employees covered by a collective bargaining agreement or those subject to other eligibility rules.

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