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Associate Formulation Scientist Jobs in New York

AMRESCO

Senior Scientist - Process Development

Bridgewater, NJ · On-site

$93K - $127K/yr

... associates/scientists. Identify and develop innovative applications for a range of products to ... Collaborate with manufacturing, quality, analytical, formulation, and regulatory teams to ensure ...

AllSTEM Connections

Scientist - I (Associate)

Rahway, NJ · On-site

$61K - $66K/yr

Experience analyzing formulation, development, characterization, or related laboratory samples ... Work is performed in a regulated scientific laboratory environment. * Candidates should be ...

Actalent

Food Scientist

East Hanover, NJ · On-site

$30 - $32/hr

Job Title: Associate Scientist We are seeking a dedicated Associate Scientist to organize and ... Understanding of scale-up and formulation processes. Work Environment This position is based in ...

Integrated Resources INC

Scientist-IV

Raritan, NJ · On-site

Prepare formulation records, testing records, SOPs and risk management plans as necessary. Prepares ... Associate Scientist level, or the equivalent training/experience. Previous experience in product ...

Syensqo

Research Scientist

Stamford, CT · On-site

$85K - $140K/yr

Practical polymer formulation and polymer processing experience preferred * Polymer Processing ... associates. Our solutions contribute to safer, cleaner, and more sustainable products found in ...

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All JobsAssociate Formulation Scientist JobsAssociate Formulation Scientist Jobs in New York

Associate Formulation Scientist information

What does an associate formulation scientist do?

An Associate Formulation Scientist is responsible for developing and optimizing formulas for products such as pharmaceuticals, cosmetics, or food items. They conduct experiments to test the stability, safety, and effectiveness of different formulations, often working under the guidance of more senior scientists. Their duties may also include documenting results, preparing reports, and collaborating with other teams such as quality control or production. This role is essential for ensuring that products meet regulatory standards and perform as intended.

What are the key skills and qualifications needed to thrive as an associate formulation scientist?

To thrive as an Associate Formulation Scientist, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by a bachelor's or master's degree. Experience with laboratory techniques, analytical instruments (like HPLC, GC), and familiarity with GLP/GMP regulations are essential. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills for this role. These skills ensure accurate formulation development, compliance with regulatory standards, and successful collaboration in a research-driven environment.

What are the typical collaboration points between an associate formulation scientist and other departments?

As an Associate Formulation Scientist, you’ll frequently collaborate with teams from analytical chemistry, quality assurance, regulatory affairs, and manufacturing. This cross-functional interaction is essential for troubleshooting formulation issues, ensuring regulatory compliance, and scaling up laboratory formulations for production. Regular meetings and project updates with these departments not only help streamline workflow but also provide valuable exposure to different areas of the product development process, fostering both learning and career growth.

What is the difference between Associate Formulation Scientist vs Formulation Scientist?

AspectAssociate Formulation ScientistFormulation Scientist
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; some roles may require 1-2 years of experienceBachelor's or master's degree; typically 2+ years of experience in formulation development
Work EnvironmentLaboratory setting, supporting formulation projects under supervisionLaboratory and development environment, leading formulation tasks
Employer & Industry UsagePharmaceutical, biotech, and cosmetic companiesPharmaceutical and biotech industries, R&D departments

The Associate Formulation Scientist role is an entry-level position supporting formulation development, often with less experience required. The Formulation Scientist typically has more experience and takes on greater responsibility in developing and optimizing formulations. Both roles are common in pharmaceutical and biotech industries, with the Associate position serving as a stepping stone to more advanced formulation roles.

What are the most commonly searched types of Formulation Scientist jobs in New York?

The most popular types of Formulation Scientist jobs in New York are:

What cities in New York are hiring for Associate Formulation Scientist jobs?

Cities in New York with the most Associate Formulation Scientist job openings:

Associate Formulation Scientist jobs near you
Infographic showing various Associate Formulation Scientist job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Senior Scientist - Process Development

Avantor Fluid Handling, LLC

Bridgewater, NJ • On-site

$93K - $127K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 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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