Analytical Chemist - II

Location: Pearl River

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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…