QC Analytical Chemist
Tris Pharma Inc
Summary
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.
Job description
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
- Bachelor's degree in Chemistry or related science field
- 0-3 years lab experience in a cGMP related industry (Associate QC Analytical Chemist)
- Hands-on experience with analytical instrumentation (UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting
- Minimum 1-5 years lab experience in a cGMP related industry (QC Analytical Chemist I)
- 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
- Minimum 2-6 years lab experience in a cGMP related industry (Chemist II)
- Minimum 3-7 years lab experience in a cGMP related industry (Chemist III)
Benefits
- Bonus
- Medical Insurance
- Dental Insurance
- Vision Insurance
- Prescription Drug Insurance
- 401(k) With Employer Match
- Life Insurance
- Paid Company Holidays
- Paid Time Off
- Paid Volunteer Time
- Employee Resource Groups
Company overview
Tris Pharma Inc is a leading privately-owned biopharmaceutical company headquartered in Monmouth Junction, New Jersey, founded in 2000. The company specializes in developing and commercializing innovative medicines for central nervous system disorders, with a particular focus on ADHD, pain management, addiction, and other neurological conditions. Tris Pharma operates through three main divisions: branded pharmaceuticals, generic medicines, and technology licensing. The company's proprietary LiquiXR® drug delivery technology underpins more than a dozen products and serves as the foundation for its stand-alone licensing business. With over 150 U.S. and international patents, Tris Pharma markets several branded and generic products in the U.S. while also licensing its technologies globally. The company employs approximately 500 professionals and maintains a robust pipeline of investigational therapies, including six clinical-stage programs targeting various CNS disorders. Tris Pharma has established itself as a market leader in multiple therapeutic categories through its patient-focused approach and commitment to developing high-quality, patient-friendly medications.