Analytical Chemist - III

Pearl River, NY
Date Posted:15-Jul-2026
Work Type:On-Site
Job Number:491872

Job Description

Job Title: Quality Control Chemist
Location: Pearl River, NY 10965
Duration: 6 Months (Possibility of extension depending upon business requirements and performance)
 
Job Description:
  • Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products.
  • This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products.
  • The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures.
 
Key Responsibilities
Perform laboratory testing of:
  • Raw materials
  • Drug substances
  • Drug products
  • In-process samples
  • Stability samples
Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including:
  • HPLC
  • GC
  • UV-Visible Spectroscopy
  • CGE
  • ICE
  • Polarimeter
  • Osmometer
  • pH Meter
  • Conductivity Meter
  • TOC Analyzer
• Accurately document and review analytical results using electronic laboratory systems (LIMS).
• Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines.
• Participate in peer review of data and laboratory documentation.
• Maintain laboratory equipment and ensure testing is performed according to approved methods.
• Support internal and external audits by maintaining thorough and compliant documentation.
• Complete required training in laboratory operations, safety procedures, and quality systems.
 
Required Qualifications:
Bachelor’s or master’s degree in:
  • Chemistry
  • Biochemistry
  • Pharmaceutical Sciences
  • Related scientific discipline
  • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment.
  • Experience within the pharmaceutical or biopharmaceutical industry is required.
  • Hands-on experience with analytical instrumentation such as HPLC, GC, and UV.
  • Strong understanding of GMP documentation practices and regulatory compliance.
  • Experience working with electronic laboratory systems and data management tools.
  • Ability to follow detailed procedures and maintain a high level of accuracy.
 
Preferred Qualifications:
  • 5-7 years of pharmaceutical QC laboratory experience.
  • Experience using Empower chromatography software.
  • Previous involvement in audit-ready environments.
  • Experience reviewing laboratory documentation and SOPs.
 
Safety Requirements:
  • This position supports testing activities involving high-potency oncology products. Candidates must be comfortable working in a controlled laboratory environment that requires:
  • Strict adherence to safety procedures.
  • Use of personal protective equipment (PPE).
  • Use of respiratory protection when required.
  • Compliance with OSHA and site-specific safety requirements.
  • All necessary training and safety equipment will be provided.
 
Training:
  • Comprehensive onboarding and GMP training provided.
  • Initial training on SOPs, documentation systems, and laboratory procedures.
  • Instrument-specific training based on assigned testing responsibilities.
  • Employees are not expected to work independently until they have successfully completed training and demonstrated competency.
 
Work Environment:
  • Primarily laboratory-based role.
  • Electronic, paperless documentation environment utilizing LIMS.
  • Combination of independent work and collaborative team support.
  • Regular interaction with quality, compliance, and laboratory personnel.
 
Additional Information:
  • Contract position with potential for long-term opportunities based on business needs and performance.
  • Interview process consists of an initial manager interview followed by a panel interview.
  • Candidates must demonstrate strong technical skills, GMP knowledge, attention to detail, and the ability to work effectively in a highly regulated pharmaceutical environment.
 

Applicant Notices & Disclaimers
  • For information on benefits, equal opportunity employment, and location-specific applicant notices, click here


At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position's pay range is $40.00/hr – $42.90/hr.