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AR&D Scientist I

Job

Tris Pharma

South Brunswick Township, NJ (In Person)

$74,000 Salary, Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 6/16/2026

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Job Description

AR D Scientist I Employer Tris Pharma Location Monmouth Junction, NJ Start date May 13, 2026 View more categories View less categories Discipline Science/R D , Biotechnology Required Education Bachelors Degree Position Type Full time Hotbed Pharm Country Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Tris Pharma, Inc. ( www.trispharma.com ) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents and market several branded ADHD products in the U.S. We also license our products in the US and ex-US markets. We have a robust pipeline of innovative products spanning neuroscience and other therapeutic categories employing our proprietary science and technology. Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris' passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company's success. Equally importance to each team member is how we interact with one another on a daily basis. We believe in each other and in respectful, open and honest communications to help support individual and team success. Our AR D lab is located in our Monmouth Junction, NJ headquarters has an immediate need for an experienced Analytical Research and Development Scientist I Summary The Analytical Research and Development (ARD) Scientist I, under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples. The incumbent also performs required maintenance and calibration of analytical instruments. Collaborating closely with, and under the direct supervision of, Senior ARD Scientists and Supervisors, she/he develops advanced analytical knowledge and expertise while carrying out laboratory work to support product development and analytical method development and performs special projects, as assigned.
ESSENTIAL FUNCTIONS
Primary duties/responsibilities
  • Carries out responsibilities in accordance with company policies, SOPs and state, federal and local laws
  • Sets up and operates analytical instruments (i.e., High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultra Violet Visible spectroscopy (UV/Vis), Thin Layer Chromatography (TLC), automatic titration, dissolution apparatus, etc.) to support sample testing
  • Performs laboratory analyses, such as blend uniformity, content uniformity, assay and dissolution, of IP, FP and ST samples per given instructions; Prepares standard and sample solutions as required by the test methods
  • Performs wet chemistry tests such as Limit of Detection (LOD), pH and titration
  • Performs physical tests such as particle size, viscosity and density measurements
  • Performs all necessary calculations associated with test analyses
  • Documents all testing details and results in laboratory notebooks compliant with current Good Documentation Practices (cGDPs)
  • Creates ARD SOPs, as needed
  • Safely and properly dispose of chemical waste, as needed
  • Cleans, maintains and calibrates laboratory instruments to ensure compliance with current Good Laboratory Practices (cGLPs) and current Good Manufacturing Practices (cGMPs)
  • Cleans and organizes ARD lab areas
  • Performs related duties, as assigned Requirements Requirements
KNOWLEDGE/SKILLS/ABILITIES REQUIRED
Minimum education and years of relevant work experience Bachelors degree in Chemistry or related science field and minimum 3 years experience in analytical/method development or method validation in the pharmaceutical or biotechnology industry OR Masters degree in Chemistry or related science field and minimum 0-3 years experience in analytical/method development or method validation in the pharmaceutical or biotechnology industry. Special knowledge or skills needed and/or licenses or certificates required
  • Understanding of spectroscopic and chromatographic techniques and concepts
  • Hands on experience in setting up and operating multiple analytical instrumentation which may include: HPLC, UV/Vis, GC, TLC and dissolution apparatus
  • Understanding and/or ability to work under cGMP, Food and Drug Administration (FDA), Drug Enforcement Administration (DEA) and Occupational Safety and Health Administration (OSHA) regulations and guidances
  • Ability to perform analytical testing and calculations, as instructed
  • Ability to perform wet chemistry and physical testings, as instructed
  • Proficiency with Microsoft Office
  • Verbal and written communication and skills
  • Ability to work independently and collaboratively, as required, in a fast paced, matrixed, team environment consisting of internal and external team members
  • Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines
  • Planning, organization and time management skills including the ability to support and prioritize multiple projects
  • Fluent in English (verbal and written)
  • Ability to identify and distinguish colors Travel requirements 0% Physical requirements Laboratory based position Ability to lift up to 30 lbs Ability to use Personal Protective Equipment (PPE) Ability to stand for extended periods of time Anticipated salary range: $63k to $85k.
Base salary offered is contingent on assessment of candidate's education and experience level relative to requirements of the position and a review of related industry standards and internal equity.
Additional benefits:
In addition to base salary, full-time employees are also eligible for incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups. Tris Pharma, Inc. offers a highly competitive compensation and benefits package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc. Tris Pharma, Inc. is an Equal Opportunity Employer. #LI-_ Company Founded in 2000, Tris Pharma, Inc. ( www.trispharma.com ) is the 3rd largest specialty pharmaceutical company in the United States. With our intense focus on the application of physical chemistry in biological systems, coupled with the requirements of manufacturing and market demands, we have grown our employee base over 250% in the past three years. Specifically, we are engaged in research, development, and manufacturing of both OTC and Rx branded products and specialty generic products. Our mission is to understand the science driving the delivery of drugs into the human body;develop and bring to market products that add value to our customers and patients and provide a benefit to our company, employees and society at large.
Company info Website https:
//www.trispharma.com/ Phone (732) 940-2800 Location US Highway 130 Monmouth Junction
NJ 08852
United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert

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