Analytical Chemist - III

Integrated Resources, Inc

Pearl River, NY

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JOB DETAILS

SALARY

SKILLS

Analysis Skills, Analytical Chemistry, Analytical Method Validation, Biochemistry, Biotech and Pharmaceutical, Chemistry, Chromatography, Communication Skills, Continuous Improvement, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Management, Data Quality, Detail Oriented, Documentation, Drug Products, Environmental Sciences, Equipment Maintenance/Repair, External Audit, Fourier-Transform Infrared Spectroscopy (FTIR), GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Identify Issues, Instrumentation, Internal Audit, Laboratory, Laboratory Equipment, Laboratory Information Management System (LIMS), Laboratory Management, Laboratory Systems, Laboratory Techniques, Laboratory Testing, Maintain Compliance, Manufacturing, Materials Analysis, Microsoft Office, Oncology, Problem Solving Skills, Procedure Development, Product Development, Product Support, Qualitative Analysis, Quality Assurance, Quality Control, Quantitative Analysis, Record Keeping, Regulatory Compliance, Reporting Skills, Research & Development (R&D), Safety Process, Standard Operating Procedures (SOP), Team Player, Technical Writing, Testing, Titration, UV/VIS (Ultraviolet-Visible Spectroscopy), Writing Skills

LOCATION

Pearl River, NY

POSTED

2 days ago

Job Title: Analytical Chemist - III
Job Location: Pearl River, NY
Job Duration: 6+ months(Contract position with potential for long-term opportunities based on business needs and performance)

Pay rate: $40.05/hr on w2

Interview: Interview process consists of an initial manager interview followed by a panel interview.

Hiring Manager Note:

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:
o Raw materials
o Drug substances
o Drug products
o In-process samples
o Stability samples
• Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including:
o HPLC
o GC
o UV-Visible Spectroscopy
o CGE
o ICE
o Polarimeter
o Osmometer
o pH Meter
o Conductivity Meter
o 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:
o Chemistry
o Biochemistry
o Pharmaceutical Sciences
o 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
• Candidates must demonstrate strong technical skills, GMP knowledge, attention to detail, and the ability to work effectively in a highly regulated pharmaceutical environment.

Summary:

The main function of an Analytical Chemist is to conduct qualitative and quantitative analysis of chemical compounds to support research, product development, and quality control.
A typical Analytical Chemist ensures the accuracy and reliability of data through method development, validation, and adherence to regulatory standards.

Job Responsibilities:

Perform chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titration.
Develop, validate, and document analytical methods for raw materials, intermediates, and finished products Interpret data, prepare technical reports, and maintain accurate laboratory records.
Ensure compliance with safety protocols, Good Laboratory Practices (GLP), and regulatory requirements (e.g., FDA, EPA).
Troubleshoot instrumentation and analytical issues to maintain data integrity.
Collaborate with cross-functional teams including R&D, QA/QC, and manufacturing.
Participate in laboratory audits and support continuous improvement initiatives.

Skills:

Strong knowledge of analytical instrumentation and techniques.
Excellent problem-solving and critical thinking abilities.
Attention to detail and high standards for data accuracy.
Proficiency in laboratory software and Microsoft Office Suite.
Effective communication and technical writing skills.
Ability to work independently and in a team-oriented environment.

Education/Experience: Bachelors degree in Chemistry, Biochemistry, or a related field required; Masters or Ph.D. preferred for advanced roles 5-7 years of experience in an analytical laboratory setting, preferably in pharmaceuticals, environmental science, or manufacturing

About the Company

Integrated Resources, Inc

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