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Analytical Chemist - II

Net2Source

Pearl River, NY

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JOB DETAILS
SALARY
$30–$32.04 Per Hour
SKILLS
Agile Programming Methodologies, Analysis Skills, Analytical Chemistry, Assays, Biochemistry, Biological Assay, Biotech and Pharmaceutical, CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing), Chemistry, Communication Skills, Data Analysis, Data Quality, Detail Oriented, Documentation, Establish Priorities, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Housekeeping/Cleaning, Industry/Trade Analysis, Instrumentation, Interpersonal Skills, Laboratory, Laboratory Analysis, Laboratory Equipment, Laboratory Information Management System (LIMS), Laboratory Notebook, Laboratory Operations, Laboratory Techniques, Laboratory Testing, Leadership, Maintain Compliance, Microsoft Excel, Microsoft Word, Organizational Skills, Polymerase Chain Reaction (PCR), Presentation/Verbal Skills, Procedure Development, Quality Assurance Methodology, Regulatory Compliance, Research & Development (R&D), Safety Process, Safety Training, Team Player, Technical Writing, Testing, Time Management, Toxicology Research, UV/VIS (Ultraviolet-Visible Spectroscopy), Writing Skills
LOCATION
Pearl River, NY
POSTED
1 day ago
Join a Global Leader in Workforce Solutions – Net2Source Inc.
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 - II
Location-Pearl River,NY,USA,10965
Duration- 6 months contract 

Position Summary
This laboratory-based position supports the Vaccine Research & Development (VRD) Analytical GLP Laboratory team. The successful candidate will perform routine sample testing,analytical method verification and qualification activities, in support early-phase vaccine toxicology studies within a highly regulated Good Laboratory Practice (GLP) environment.
The ideal candidate will have prior pharmaceutical or biotechnology laboratory experience, strong documentation skills, and the ability to work collaboratively within a small, highly engaged analytical team.
This role offers a balanced workload consisting of approximately:
• 50% laboratory-based analytical testing
• 50% data analysis, documentation, and report writing

Key Responsibilities
• Perform routine sample testing in support of GLP release and stability studies for vaccine candidates.
• Execute analytical method verification and qualification studies under guidance.
• Prepare samples, operate analytical instrumentation, and generate high-quality data.
• Analyze experimental results and document findings in compliance with GLP and Good Documentation Practices (GDP).
• Record laboratory activities contemporaneously using Electronic Laboratory Notebooks (ELN).
• Draft, review, and revise laboratory methods, reports, and technical documentation.
• Support assay transfer, training activities, and method implementation.
• Plan and prioritize daily laboratory activities to meet project timelines.
• Follow laboratory procedures, safety requirements, and compliance standards.
• Participate in laboratory maintenance activities, including equipment upkeep and laboratory housekeeping.
• Communicate testing issues, deviations, and observations appropriately to management.

Preferred Technical Experience
Candidates should have experience with some combination of the following:
Bioanalytical Assays
• ELISA • MSD (Meso Scale Discovery) • PCR-based techniques • Slot Blot
Analytical Instrumentation
• UV-Visible Spectroscopy (UV-Vis) • HPLC-UV • HPLC-CAD • Flow Analysis (FA)

Additional Preferred Skills
• Hamilton automated systems (nice-to-have)
• Laboratory Information Management Systems (LIMS) (nice-to-have)
• Electronic Laboratory Notebooks (ELN)
• Microsoft Excel and Word for data analysis and technical documentation

Education Qualifications
• BS in Chemistry, Biochemistry or related discipline plus 2 or more years of related work experience, or MS in Chemistry, Biochemistry or related discipline and 0-2 years of experience. 
• Experience in bioassays (MSD, PCR-based techniques, Slot Blot), spectroscopic techniques (UV-VIS.) and separation-based analytical techniques (HPLC-UV, HPLC-CAD) is preferred. 
• Good interpersonal, verbal and written skills. 
• Motivated, detail-oriented, with good laboratory skills.

Experience Preferred:
• At least one year of pharmaceutical, biotechnology, or industrial laboratory experience.
• Experience working in a regulated environment (GLP, GMP, or similar).
• Familiarity with compliance-driven laboratory operations and documentation practices.
Academic laboratory experience alone may be considered; however, industry laboratory experience is strongly preferred due to the regulated nature of the work.

Required Competencies
• Strong written and verbal communication skills.
• Excellent documentation and technical writing abilities.
• Detail-oriented with a strong focus on quality and compliance.
• Ability to analyze data and draw scientifically sound conclusions.
• Strong organizational and time-management skills.
• Willingness to learn and follow established procedures.
• Effective team player with good interpersonal skills.
• Reliable attendance and professional work ethic.

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 Agile1

About the Company

N

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.
COMPANY SIZE
50 to 99 employees
INDUSTRY
Other/Not Classified
WEBSITE
http://www.net2source.com