QC Analytical Chemist Employer Tris Pharma Location Monmouth Junction, NJ Start date Jul 11, 2026 View more categories View less categories Discipline Information Technology , Business/Data Analytics , Science/R D , Chemistry 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 Quality Control Department is growing and we have openings for QC Analytical Chemists at various levels requiring multiple levels of experience. Title and salary commensurate with experience. These are 1st shift position working Monday-Friday in our Monmouth Junction, NJ laboratories.

ESSENTIAL FUNCTIONS

Carries out responsibilities in accordance with company policies, SOPs and state, federal and local laws Performs testing of raw materials, in-process (IP), finished products (FP) and/or stability sample (ST) samples including dissolution, assay, content/blend uniformity, particle size distribution and other tests according to the analytical methods, USP procedures in a regulated laboratory environment. Chemist I also performs analytical method transfers and method verifications Analyzes and interprets test results Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and dissolution apparatus (Distek) Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations Complies with all company policies and procedures, including safety rules and regulations Adheres to GMPs and current Good Documentation Practices (GDPs) Requirements Associate QC Analytical Chemist - Bachelors degree in Chemistry or related science field and 0-3 years lab experience in a cGMP related industry. Hands-on experience with analytical instrumentation (i.e., UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting Anticipated salary range: $60-65k/yr. QC Analytical Chemist I -Bachelor's Degree in Chemistry or related science field and minimum 1-5 years lab experience in a cGMP related industry. Hands-on experience with analytical instrumentation (i.e., UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical or biotechnology setting Strong hands-on experience performing and interpreting Related Compounds analysis (Impurity analysis) Demonstrated ability to apply good laboratory techniques while maintaining efficiencies required in a QC lab Anticipated salary range: $65-75k/yr.. Chemist II - Bachelors degree in Chemistry or related science field and minimum 2-6 years lab experience in a cGMP related industry.

Anticipated salary range:

$75-85k/yr. Chemist III - Bachelors degree in Chemistry or related science field and minimum 3-7 years lab experience in a cGMP related industry.

Anticipated salary range:

$80-90k/yr. 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, all 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-onsite 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

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