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Analytical Scientist

Job in Trenton, Mercer County, New Jersey, 08628, USA
Listing for: Kelly Science, Engineering, Technology & Telecom
Full Time position
Listed on 2026-02-12
Job specializations:
  • Research/Development
    Research Scientist, Biotechnology, Data Scientist
Salary/Wage Range or Industry Benchmark: 90000 - 95000 USD Yearly USD 90000.00 95000.00 YEAR
Job Description & How to Apply Below

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Kelly Science, Engineering, Technology & Telecom provided pay range

This range is provided by Kelly Science, Engineering, Technology & Telecom. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$90,000.00/yr - $95,000.00/yr

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Scientific Recruiter @ Kelly Science | Staffing, Biotech, Pharma, Clinical

Job Title:
Scientist – Analytical R&D

Position Summary:

The Scientist, Analytical R&D, is responsible for providing hands-on analytical support for method development, validation, and transfer activities within the Analytical R&D team, with minimal supervision. This role may also serve as a project lead, overseeing analytical method optimization, evaluation, and stability studies using a range of laboratory techniques and instrumentation.

Key Responsibilities:

  • Independently perform analytical method development, optimization, improvement, and validation using techniques such as HPLC, GC, Dissolution, UV-Vis Spectroscopy, FTIR, Microscopy, Particle Size Distribution (PSD), etc.
  • Conduct method evaluations, pre-validation activities, and informal stability sample testing.
  • Assist in complex studies, including impurity identification and excipient compatibility assessments.
  • Prioritize and execute analytical activities to support product development timelines.
  • Identify potential analytical challenges early in the R&D process and contribute to strategic planning for method development and improvement.
  • Support formulation development and technology transfer efforts for assigned projects.
  • Investigate method performance issues, conduct troubleshooting, and lead optimization studies.
  • Draft and review technical documentation such as validation protocols/reports, analytical procedures, and reference standard qualification reports.
  • Develop and revise Standard Operating Procedures (SOPs) as assigned.
  • Stay current with scientific literature and trends related to analytical technologies and regulatory expectations.
  • Uphold company standards for data integrity and adhere to GxP and regulatory requirements.

Qualifications:

Education & Experience:

  • Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline with a minimum of 6 years of relevant analytical chemistry experience, or
  • Master’s degree in Chemistry, Biochemistry, or a related scientific discipline with a minimum of 4 years of relevant experience.
  • Industry experience in the pharmaceutical or biopharmaceutical sector is preferred.
  • Demonstrated knowledge of GxP, ICH, and compendial requirements (e.g., USP, EP, JP).

Technical Skills:

Proficiency with laboratory instrumentation and software, including but not limited to:

  • HPLC (Empower software preferred)
  • GC (solvent testing)
  • Dissolution testing
  • Assay and impurity analysis
  • UV-Vis, FTIR, Microscopy, PSD
  • Familiarity with GMP systems and documentation practices.
  • Experience with solid oral dosage forms required; familiarity with soft gels or liquid dosage forms is a plus.
Seniority level
  • Seniority level Associate
Employment type
  • Employment type

    Full-time
Job function
  • Job function

    Science, Research, and Manufacturing
  • Industries Biotechnology Research, Pharmaceutical Manufacturing, and Research Services

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Pension plan

Disability insurance

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