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Associate Formulation Scientist Jobs in Bridgewater, NJ

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 ...

Showing results 21-40

Associate Formulation Scientist information

See Bridgewater, NJ salary details

$20

$38

$74

How much do associate formulation scientist jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for associate formulation scientist in Bridgewater, NJ is $38.45, according to ZipRecruiter salary data. Most workers in this role earn between $25.82 and $44.47 per hour, depending on experience, location, and employer.

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 cities near Bridgewater, NJ are hiring for Associate Formulation Scientist jobs?

Cities near Bridgewater, NJ with the most Associate Formulation Scientist job openings:

Associate Principal Scientist, Hybrid Modeler, Digital Insights, DSCS Digital Technologies

MSD

Rahway, NJ • Hybrid

$59K - $60K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Job description

Job Description

We are a global biopharmaceutical leader with a different portfolio of prescription medicines, oncology, vaccines and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state-of-the-art laboratories, plants and offices that are designed to inspire our employees as we learn, develop and grow in our careers. We are proud of our over 125 years of service to humanity and continue to be one of the world's biggest investors in Research & Development.

We are seeking an Associate Principal Scientist to join our Digital Insights team within the Development Sciences and Clinical Supply (DSCS) Digital Technologies organization. Digital is the multiplier that will allow DSCS to deliver better experiments faster, efficient filing and launch, more robust supply chains and higher-confidence decisions across the portfolio.

The DSCS Digital Technologies organization is responsible for the invention and application of new digital tools/workflows to support scientists across drug substance development, drug product development and analytical development. We aspire to embed digital technologies into the fabric of DSCS culture to drive transformational impact. The tools that we develop are as different as the teams developing them, and in this Associate Principal Scientist role, the successful candidate will advance the company's digital-first process development strategy by deploying mechanistic, CFD-based, and data-driven modeling approaches to design, de-risk, and optimize sterile drug substance (DS) and drug product (DP) manufacturing processes. The position will sit at the intersection of first-principles physics, advanced CFD, and machine learning / data science, enabling predictive understanding, robust scale-up, and accelerated clinical-to-commercial delivery across biologics and vaccines.

The successful candidate will play a technical leadership role in building and applying mixing and unit-operation virtual twins, integrating CFD with experimental data and AI/ML methods, and translating model outputs into actionable CMC and manufacturing decisions.

Responsibilities:

  • Develop and deploy a portfolio of mechanistic, CFD, and data-driven models to support development, scale-up, tech transfer, and manufacturing of sterile DS and DP processes across a different biologics and vaccine pipeline.
  • Lead CFD-based mixing and unit operation modeling (e.g., compounding, dilution, pumping, filling, filtration) to quantify hydrodynamic stresses, energy dissipation rates, mixing times, and scale-up risk-enabling science-based operating windows and control strategies.
  • Integrate data science and machine learning with physics-based models to accelerate model execution, improve predictive accuracy, and enable rapid scenario screening.
  • Collaborate closely with Sterile Product Development (SPD), Drug Substance, Manufacturing Science and Technology (MS&T), and Manufacturing teams to de-risk sterile process scale-up, optimize formulation and process robustness, and support clinicaltocommercial transitions across both small and large molecule modalities.
  • Design, execute, and interpret scaledown and validation experiments to establish model credibility and scalability. Use experimental data to validate and refine CFD and ML models.
  • Provide technical leadership during critical investigations, including deviations, root-cause analyses, and process troubleshooting, using model-based insights to rapidly resolve product and process challenges.
  • Own end-to-end modeling project execution, including problem formulation, data requirements, simulation workflows, model validation, reporting, and clear communication of predictions and uncertainty to crossfunctional stakeholders.
  • Establish best practices for modeling workflows, including pre/postprocessing, HPC and cloud computing utilization, data management, version control, and model reuse. Contribute to standardized playbooks and a central model repository.
  • Demonstrate excellent interpersonal, communication, and collaboration skills.
  • Embrace and model our core values of inclusion, including fostering a supportive culture where all can thrive.
  • Be able to effectively collaborate in a dynamic, integrated, and multidisciplinary team environment.
  • Demonstrate a clear ability to perform impactful scientific innovation in a team-oriented manner that builds trusted partnerships across vast stakeholder networks.
  • Contribute to the broader scientific community and enhance the company's reputation through a strong record of peer-reviewed publications and impactful conference presentations.

Education Minimum Requirement:

  • Ph.D. in Computer Science, Data Science, Engineering, Chemistry, Physics, Biology, Pharmaceutical Sciences, or a closely-related field with at least 3 years of industrial/pharmaceutical or relevant experience.
  • M.S. in Computer Science, Data Science, Engineering, Chemistry, Physics, Biology, Pharmaceutical Sciences, or a closely-related field with at least 5 years of industrial/pharmaceutical or relevant experience.
  • B.S. in in Computer Science, Data Science, Engineering, Chemistry, Physics, Biology, Pharmaceutical Sciences, or a closely-related field with at least 7 years of industrial/pharmaceutical or relevant experience.

Required Experience and Skills:

  • Strong expertise in CFD and transport phenomena, with hands-on experience using tools such as ANSYS Fluent, STARCCM+, MStar, COMSOL, OpenFOAM, or equivalent.
  • Demonstrated experience with multiphase and complex flows, including freesurface modeling (VOF), turbulent flows, nonNewtonian rheology, and/or particleladen systems.
  • Strong programming and data science skills in Python, MATLAB, R, JMP, or equivalent, including data wrangling, visualization, model coupling, and workflow automation.
  • Experience validating models against experimental data and designing representative scaledown systems.
  • Ability to translate complex modeling results into clear, actionable insights for nonmodeling audiences; strong written and verbal communication skills.

Preferred Experience and Skills:

  • Experience with sterile CMC development workflows, particularly unit operations such as mixing, pooling, pumping, filling, filtration, or freezedrying.
  • Familiarity with regulatory expectations and trends supporting mechanistic modeling, digital twins, and modelinformed development in cGMP environments (e.g., ICH Q8-Q12, CFR, USP).
  • Applied understanding of QbD, DOE, and model validation frameworks, including statistical design and analysis of experiments.
  • Working knowledge of multivariate data analysis, SPC, and PAT, with experience integrating experimental and manufacturing data into models.
  • Experience with advanced modeling approaches, such as:
    • Reducedorder modeling (ROM)
    • Physicsinformed neural networks (PINNs)
    • Hybrid mechanistic / machine learning models
    • CFDML surrogate models for rapid decision making
  • Prior contributions to technology transfer, process robustness assessments, or troubleshooting using modeling and simulation are a strong plus.

Required Skills:

Adaptability, Adaptability, Analytical Method Development, Artificial Neural Networks (ANNS), Assay Development, Biological Assay Development, Cell-Based Assays, Chromatographic Techniques, Cross-Functional Teamwork, Data Merging, Data Modeling Techniques, Design of Experiments (DOE), External Collaboration, High Performance Computing (HPC), High Resolution Mass Spectrometry (HRMS), Liquid Chromatography-Mass Spectrometry (LC-MS), Machine Learning (ML), Mass Spectrometry Analysis, Mathematics Modeling, MATLAB, Model Building, Model Development, Neural Networks, Optimism, Perform Testing {+ 10 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$142,400.00 - $224,100.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

09/4/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.