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Formulation Manager Jobs in Edison, NJ (NOW HIRING)

USPL NUTRITIONALS LLC

Associate, R&D

North Brunswick, NJ · On-site

$25 - $30/hr

Date 12/2025 Location 1300 Airport Road, North Brunswick NJ Title Associate, R&D Formulation Department R&D Reports to Manager, R&D FLSA (Exempt or Non-Exempt) Non-Exempt Role Overview The Associate ...

Reliance Private Label Supplements

Be Seen First

R&D Scientist (9am - 5pm)

Edison, NJ · On-site

$60K - $65K/yr

Formulation Development * Innovation & Continuous Improvement * Effective Communication * Teamwork & Collaboration * Planning & Time Management * Customer Focus * Accountability & Ownership Working ...

Kenvue

Senior Scientist- Self Care

Summit, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

Kenvue

Senior Scientist- Self Care

Chatham, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

Kenvue

Senior Scientist- Self Care

Short Hills, NJ

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

Kenvue

Senior Scientist- Self Care

Mountainside, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

Kenvue

Senior Scientist- Self Care

Summit, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

Kenvue

Senior Scientist- Self Care

Springfield, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

Kenvue

Senior Scientist- Self Care

New Providence, NJ · On-site

$105K - $148K/yr

... formulation and/or process development expertise who can lead and execute R&D projects focused on creating and optimizing self-care solutions. The successful candidate will manage multiple projects ...

New

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Formulation Manager information

See Edison, NJ salary details

$14

$23

$43

How much do formulation manager jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for formulation manager in Edison, NJ is $23.64, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $23.65 per hour, depending on experience, location, and employer.

What is a formulation manager?

Formulation Managers are professionals responsible for overseeing the development and optimization of product formulations, particularly in industries like pharmaceuticals, cosmetics, food, and chemicals. They lead teams to design, test, and refine product mixtures to meet quality, safety, and regulatory standards. Their role often involves coordinating with research, production, and quality assurance departments to ensure that product formulations are effective, stable, and cost-efficient. Formulation Managers also stay updated on industry trends and regulatory changes to keep their company's products competitive. Effective communication, project management, and technical expertise are key skills for this role.

What are some common challenges faced by a formulation manager in coordinating cross-functional teams?

Formulation Managers often work closely with R&D, quality assurance, regulatory, and production teams to bring new products from concept to launch. A common challenge is ensuring clear communication and alignment across departments, especially when dealing with tight timelines or shifting project priorities. Balancing technical requirements, regulatory compliance, and manufacturing feasibility can also be demanding. Successful Formulation Managers are proactive in problem-solving and skilled at fostering strong collaboration to keep projects on track.

What are the key skills and qualifications needed to thrive as a formulation manager, and why are they important?

To thrive as a Formulation Manager, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by an advanced degree and experience in product formulation. Familiarity with laboratory equipment, formulation development software, and regulatory compliance systems is typically required. Strong leadership, problem-solving, and project management skills help you effectively lead teams and navigate complex product development cycles. These competencies are crucial for ensuring product quality, regulatory adherence, and timely delivery of innovative formulations.

What is the difference between Formulation Manager vs Formulation Scientist?

AspectFormulation ManagerFormulation Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmacy, or related field; often requires experience in project managementBachelor's or Master's in Chemistry, Pharmacy, or related field; focus on research skills
Work EnvironmentOversees teams in R&D or manufacturing settings, manages projects, and coordinates formulation developmentConducts laboratory research, experiments, and formulation testing
Industry UsageCommonly used in pharmaceutical, cosmetics, and chemical industries for leadership rolesPrimarily used in research and development departments for formulation development

The Formulation Manager typically oversees formulation projects, manages teams, and ensures product development aligns with business goals. In contrast, the Formulation Scientist focuses on conducting experiments and developing formulations in the lab. Both roles require similar educational backgrounds but differ in responsibilities and scope within the formulation process.

What cities near Edison, NJ are hiring for Formulation Manager jobs? Cities near Edison, NJ with the most Formulation Manager job openings:
Formulation Manager jobs near you
Infographic showing various Formulation Manager job openings in Edison, NJ as of August 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $49,162 per year, or $23.6 per hour.

Associate, R&D

USPL NUTRITIONALS LLC

North Brunswick, NJ • On-site

$25 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Job description

Job Description

Date

12/2025

Location

1300 Airport Road, North Brunswick NJ

Title

Associate, R&D Formulation

Department

R&D

Reports to

Manager, R&D

FLSA (Exempt or Non-Exempt)

Non-Exempt

Role Overview

The Associate, R&D Formulation serves as a transitional position between an advanced R&D technician and a Formulator -1. This role requires hands-on execution combined with growing technical ownership of formulation development activities. The individual will lead formulation experiments, support process development and scale-up, and ensure compliant documentation while demonstrating readiness to advance into a Formulator role.

Areas of Responsibility

Formulation Development & Execution

  • Support formulation experiments for new product development and optimization of existing products.
  • Design and prepare prototypes and experimental batches at benchtop, pilot, and scale-up levels.
  • Support development of solid oral dosage forms (tablets, capsules, granules).
  • Execute formulation activities independently with minimal supervision while escalating complex challenges appropriately.
  • Collaborate closely with and support senior R&D team members in daily product development activities.

Process Development & Scale-Up

  • Support process development, validation, troubleshooting, and technology transfer to manufacturing.
  • Execute pilot-scale and scale-up batches to support commercialization.
  • Partner with Manufacturing and Engineering teams to optimize processes.

Equipment Operation & Technical Ownership

  • Set up, operate, clean, and perform changeovers on R&D and pilot-scale equipment, including:
    • Tablet presses
    • Capsule filling machines
    • Coating equipment
    • Granulators
    • Fluid Bed Dryers (FBDs)
  • Ensure equipment is maintained and operated in compliance with SOPs, safety standards, and cGMP requirements.
  • Troubleshoot equipment and process issues using strong technical and analytical skills.

Documentation, Compliance & Communication

  • Maintain accurate and compliant documentation (BMRs, logbooks, protocols, reports).
  • Record formulation data, observations, and changes in a timely and clear manner.
  • Ensure adherence to cGMP, SOPs, and regulatory requirements.
  • Communicate updates, results, and project status effectively to R&D and cross-functional teams.
  • Prepare and review technical and customer-facing documents, including:
    • Sample shipment cover letters
    • Commercial invoices and declaration documents for international shipments
    • Tracking and data analysis spreadsheets

Cross-Functional Coordination & Operations

  • Coordinate with internal departments to support smooth R&D operations:
    • QC: Sample drop-off and documentation
    • QA: Sample testing, shipment coordination, and results tracking
    • Packaging: Sample transfer and packaging
    • Warehouse/Inventory: Material availability and tracking
    • Purchasing: Requisitions, POs, and delivery timelines
    • Maintenance: Equipment and facility repairs
    • External Facilities (e.g., VanDyke Building): Raw material transfers
  • Request materials through Syspro and ensure availability for trials.
  • Schedule and coordinate meetings across R&D and Purchasing teams.

Sample Management, Packaging & Shipping

  • Package, label, and maintain inventory of samples for:
    • Customer evaluations and meetings
    • Internal and external testing
    • Stability studies
  • Ship samples, materials, and documents via FedEx and UPS, including international shipments.
  • Prepare all required shipping documentation and ensure compliance with international regulations.
  • Coordinate with shipping carriers to resolve delays and ensure timely delivery.

Inventory, Warehouse & Material Management

  • Maintain organization, labeling, and safety of R&D warehouse and storage areas.
  • Ensure proper labeling and storage of raw materials, packaging materials, and supplier samples.
  • Manage controlled storage requirements (e.g., probiotics in designated rooms/freezers).
  • Track inventory levels, material usage, and delivery timelines.
  • Maintain office and lab supply inventory.

Data Tracking & Administrative Support

  • Packages & labels samples for shipments & customer review.
  • Packages all samples for customer meetings & maintains inventory for sample presentation.
  • Packages & labels samples for internal & external testing.
  • Packages & labels samples occasionally for stability trials.
  • Maintains warehouse organization & safety
  • Labels raw materials correctly & maintains organization system for each section of the warehouse.
  • Labels packaging materials to ensure easy retrieval.
  • Labels supplier received raw materials with necessary information for easy retrieval.
  • Ensures probiotic samples are correctly stored in R&D probiotic room or freezer.
  • Ships samples, materials, & documents via FedEx & UPS
  • Ships samples to customers for sample & document review
  • Ships samples to external labs for testing along with sample requisitions.
  • Ships samples internationally, ensuring all documentation required for other countries is provided.
  • Works externally with Fedex/UPS representatives to ensure delayed packages are delivered & documentation is updated correctly.
  • Create, Compose, edits, & reviews written material as necessary to share with appropriate internal departments & customers.
  • Composes cover letters for customer sample shipments
  • Composes required documents for international shipments, such as declaration letters, commercial invoices, & cover letters.
  • Creates excel sheets for tracking & comparison purposes.
  • Reviews material documents to ensure proper storage.
  • Maintains Excel logs for the following:
  • Received raw material from 1300.
  • Incoming sample raw material from suppliers.
  • In-house QC samples for testing & results.
  • External lab sample testing & results.
  • Samples shipped to customers via FedEx & UPS.
  • Creates requisitions through purchasing team & receives Purchase Orders as necessary
  • Creates requisitions & receives PO’s through Syspro.
  • Monitors purchased materials for all R&D projects & keeps track of all raw material delivery ETA’s
  • Reviews invoices for approval for shipping, lab testing, & other external purchases.
  • Maintains office supply inventory regularly.

Continuous Improvement & Development

  • Identify opportunities to improve formulation, processes, and operational efficiency.
  • Participate in 5S, safety, and continuous improvement initiatives.
  • Demonstrate increasing ownership and decision-making to prepare for advancement.

Additional Responsibilities

  • Follow all lab safety and PPE requirements.
  • Provide guidance and mentorship to junior technicians.
  • Perform other duties as assigned to support business objectives.

Requirements

Education & Qualification:

  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biology, or a related scientific field preferred (or equivalent hands-on experience).
  • 1–3 years of experience in pharmaceutical R&D formulation, pilot-scale manufacturing, or related technical roles.
  • Minimum of three (3) years of work experience in nutritionals, supplements, food, or pharmaceutical manufacturing industries.
  • Experience with formulation development (e.g., liquids, powders, tablets, gels, capsules, etc., depending on your industry).
  • Strong understanding of formulation principles, laboratory techniques, and scientific methods.
  • Excellent documentation, organizational, and time-management skills.
  • Ability to interpret data, identify trends, and propose scientifically sound conclusions.
  • Strong communication and teamwork abilities.
  • Proficient with Microsoft Office and lab software (LIMS, ELN, etc., if applicable).
  • Hands-on experience with any of the following processes: Blending/Granulation, Tablet Compression and/or Film Coating, Encapsulation, or Pharmacy/Pre-Weigh Dispensing

Certifications, Licenses, Credentials:

  • N/A

Skills & Ability

  • Demonstrates ability to work in a team and assist others.
  • Able to follow written instructions precisely and perform basic math calculations as required.
  • Understands and is knowledgeable of cGMP, OSHA standards etc.
  • Mechanically inclined to understand inner workings of equipment.
  • Knowledge of any of the following processes: Blending/Granulation, Tablet Compression and/or Film Coating, Encapsulation, or Pharmacy/Pre-Weigh Dispensing.
  • Demonstrates the ability to read and write English in order to be able to understand the industry regulated instruction sheets.
  • Has experience with the following: Google Suite, Microsoft Excel, Word, PowerPoint, & Teams, Syspro8

Physical Requirements (lifting, etc.):

  • Ability to lift up to 50 lbs.; occasionally lift and move up to 75 pounds.
  • Must stand and walk on the production floor for a minimum of 6 hours per shift
  • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances.
  • Occasionally works from a rolling ladder or step stool, must be to lean over equipment as well as kneeling on the floor to clean under the equipment.
  • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators.


Work Environment (Office, Warehouse, temperature extremes, etc.):

  • Work is regularly performed inside a manufacturing environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate.
  • Employees can be exposed daily to chemicals and cleaning agents.

The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship.

USPL is proud to be an Equal Opportunity Employer.

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law.

Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment.


Job Description Acknowledgement


I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodation.

This Job Description has been reviewed with my supervisor.