QC Scientists

Ocimpharma; New Jersey; On-site; USD 83,000 - 87,000; Full time

Benefits offered by this job

Standard benefits

Job summary

Ocimpharma in Pine Brook, NJ is seeking a chemist to conduct quality control testing of raw materials, in-process, and finished pharmaceutical products using HPLC/UPLC, GC-HS, UV spectrometry, and dissolution. You will prepare, review, and execute analytical method validations, transfer protocols, CAPA investigations of OOS results, and maintain lab records with rigorous data interpretation.

The role requires a Master’s degree in Chemistry or Pharmaceutical Chemistry and practical expertise in

Qualifications

• Master’s degree in Chemistry or Pharmaceutical Chemistry is required.
• Experience with HPLC, GC, UV spectrometry, dissolution and related analytical methods is essential.
• Understanding of method verification, validation and transfer protocols is preferred.

Responsibilities

• Conduct quality control chemical testing of materials and products using HPLC/UPLC, GC-HS, UV spectrometry, and dissolution.
• Prepare, review and execute analytical methodologies, method verification/validation, transfer protocols and reports.
• Investigate out-of-specification (OOS) laboratory results using CAPA and OOS/OOT frameworks.
• Maintain laboratory records and interpret data using statistical principles.
• Maintain and troubleshoot analytical equipment and coordinate qualification and calibration activities.

Skills

HPLC

GC

UV Spectrometry

Dissolution

Particle size analysis

Analytical Methodologies

Education

Master’s degree in Chemistry/Pharmaceutical Chemistry

Job description

Job Responsibilities

• Conduct quality control chemical testing of raw materials, in-process, and finished pharmaceutical products using HPLC/UPLC, GC-HS, UV Spectrometry, physicochemical characterization, Particle size analysis, and in-vitro drug release testing;
• Prepare, review, and execute technical documentation, including Analytical methodologies, method verification, validation, and transfer protocols, and reports and SOPs;
• Perform investigations of out-of-specification (OOS) laboratory results using OOS/OOT, CAPA;
• Maintain laboratory record and interpret data using statistical principles;
• Maintain and troubleshoot analytical equipment and coordinate equipment qualification and calibration activities using AAS (Atomic Absorption Spectroscopy) and Dissolution.

Requirements

• Require Master’s degree in Chemistry or Pharmaceutical Chemistry plus skills and knowledge in HPLC, GC, UV Spectrometry, Analytical Methodologies, Dissolution, Particle size analysis.

Job location: Pine Brook, NJ.

Standard benefits with $83k~$87k/year.