Analytical Scientist

Kelly Science, Engineering, Technology & Telecom

New Jersey

On-site

USD 90,000 - 95,000

Full time

14 days+

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Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Pension plan

Disability insurance

Job summary

A leading company in biotechnology is seeking a Scientist for Analytical R&D. This role involves hands-on analytical support for method development and validation, requiring expertise in various laboratory techniques. The ideal candidate will have a strong background in analytical chemistry and experience in the pharmaceutical sector. Responsibilities include method optimization, troubleshooting, and documentation. Join a dynamic team dedicated to advancing scientific research and product development.

Qualifications

Minimum 6 years relevant analytical chemistry experience with a Bachelor’s degree.
Industry experience in pharmaceutical or biopharmaceutical sector preferred.

Responsibilities

Perform analytical method development and validation with minimal supervision.
Conduct method evaluations and assist in complex studies.

Skills

Analytical Chemistry

Problem Solving

Data Integrity

Education

Bachelor’s degree in Chemistry

Master’s degree in Chemistry

Tools

HPLC

UV-Vis

FTIR

Microscopy

Job description

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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

Direct message the job poster from Kelly Science, Engineering, Technology & Telecom

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