QC Analytical Chemist

Tris Pharma Inc•South Brunswick, NJ

99d•Onsite

About The Position

Tris Pharma, Inc. is a privately-owned U.S. biopharmaceutical company focused on developing and commercializing innovative medicines in areas such as ADHD, spectrum disorders, anxiety, pain, and addiction. The company holds over 150 U.S. and international patents and markets several branded ADHD products in the U.S., while also licensing products domestically and internationally. Tris Pharma has a strong pipeline of innovative products in neuroscience and other therapeutic categories, utilizing proprietary science and technology. The company values its team members, emphasizing their role in driving passion and innovation, and fostering a culture of respectful, open, and honest communication to support individual and team success. The Quality Control Department is expanding, with openings for QC Analytical Chemists at various levels, requiring diverse experience. These are first-shift positions, Monday-Friday, located in the Monmouth Junction, NJ laboratories.

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.
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.
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.

Responsibilities

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).