Jobs · Information Technology · New Jersey

QC Analytical Chemist

BioSpace · Monmouth Junction, NJ · 1 mo ago
On-siteInformation TechnologyFull-time

About the role

Tris Pharma, Inc. is seeking QC Analytical Chemists at various levels to join our Quality Control Department. Positions are available in Monmouth Junction, NJ and offer competitive salaries based on experience.

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
  • 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
  • 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

Qualifications

  • Bachelor’s Degree in Chemistry or related science field
  • Minimum 0-7 years lab experience in a cGMP related industry

Skills

  • Hands-on experience with analytical instrumentation (i.e., UV, IR, HPLC, GC and/or dissolution instruments)
  • Good laboratory techniques
  • Interpretation of analytical data
  • Problem-solving skills

Benefits

  • Incentives
  • Medical, dental, vision, Rx insurance
  • 401K with match
  • Life insurance
  • Paid Company Holidays
  • PTO
  • Paid Volunteer Time
  • Employee Resource Groups

Pay

  • 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.

Schedule

  • 1st shift working Monday-Friday

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