QC Analytical Chemist
Job in
South Brunswick, Middlesex County, New Jersey, USA
Listed on 2026-07-18
Listing for:
BioSpace
Full Time
position Listed on 2026-07-18
Job specializations:
-
Science
Analytical Chemist, Pharmaceutical Science/ Research, Chemistry, Lab Tech / Assistant -
Quality Assurance - QA/QC
Job Description & How to Apply Below
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), ultraviolet visible spectroscopy (UV/Vis), automatic titration, infrared 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).
- Associate QC Analytical Chemist – Bachelor’s 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 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 – Bachelor’s degree in Chemistry or related science field and 2‑6 years lab experience in a cGMP related industry.
- Anticipated salary range: $75‑85k/yr.
- Chemist III – Bachelor’s degree in Chemistry or related science field and 3‑7 years lab experience in a cGMP related industry.
- Anticipated salary range: $80‑90k/yr.
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, prescription insurance, 401(k) with match, life insurance, paid company holidays, paid time off, paid volunteer time and employee resource groups.
Tris Pharma, Inc. is an Equal Opportunity Employer. We encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc.
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