Agile Programming Methodologies, Analysis Skills, Analytical Chemistry, Biochemistry, Biotech and Pharmaceutical, Chemistry, Chromatography, Current Good Manufacturing Practice (cGMP), Data Management, Detail Oriented, Documentation, Drug Products, Equipment Maintenance/Repair, External Audit, GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Industry/Trade Analysis, Instrumentation, Internal Audit, Laboratory, Laboratory Equipment, Laboratory Information Management System (LIMS), Laboratory Management, Laboratory Systems, Laboratory Techniques, Laboratory Testing, Leadership, Maintain Compliance, Materials Testing, Oncology, Procedure Development, Quality Control, Regulatory Compliance, Safety Process, Sample/Specimen Processing, Standard Operating Procedures (SOP), Team Player, Test Lab, Testing, UV Spectroscopy
Who We Are
Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision Right Talent. Right Time. Right Place. Right Price.
Title-Analytical Chemist - III
Location-Pearl River,NY,USA,10965
Duration- 6 months contract - 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.
Why Work With Us?
We believe in more than just jobs we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity
Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.
Awards & Recognition
" America's Most Honored Businesses (Top 10%)
" Fastest-Growing Staffing Firm by Staffing Industry Analysts
" INC 5000 List for Eight Consecutive Years
" Top 100 by Dallas Business Journal
" Spirit of Alliance Award by Agile1N
Net2Source
Net2Source Inc. is a Global Workforce Management Solutions Company, headquartered in New Brunswick, NJ with its local offices in Texas, California, Florida, Illinois, Colorado and Michigan and its global operations in Canada, UK, Europe, UAE, Malaysia, Australia, China, Singapore and India. Net2Source offers a wide gamut of consulting solutions customized to specific client needs including but not limited to Application Development, Workforce Management and Project Consulting.
Whether it’s a Fortune client, whether it’s a System Implementer or whether it is a Start -up, our recipe to success – Exceed expectations! Under promise, over deliver.
50 to 99 employees
http://www.net2source.com