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:
Key Responsibilities
Perform laboratory testing of:
• 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:
Preferred Qualifications:
Safety Requirements:
Training:
Work Environment:
Additional Information:
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
- HPLC
- GC
- UV-Visible Spectroscopy
- CGE
- ICE
- Polarimeter
- Osmometer
- pH Meter
- Conductivity Meter
- TOC Analyzer
• 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.