QC Lab Analytical Chemist

Tris Pharma, Inc. ( 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 USand International patents and market several branded ADHD products in the U.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. 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. These are 1st shift position working Monday-Friday in our Monmouth Junction, NJ laboratories.

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

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)

Complies with all company policies and procedures, including safety rules and regulations

Associate QC Analytical Chemist - Bachelors degree in Chemistry or related science field and 0-3 years lab experience in a cGMP related industry.

UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting

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.

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

Chemist II - Bachelors degree in Chemistry or related science field and minimum 2-6 years lab experience in a cGMP related industry.

Chemist III - Bachelors degree in Chemistry or related science field and minimum 3-7 years lab experience in a cGMP related industry.

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.

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. #