Analytical Chemist I – Pharma QC & Method Development

bostonanalytical

New Hampshire

On-site

USD 42,000 - 54,000

Full time

14 days+

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Job summary

BA Sciences is seeking a Chemist to conduct qualitative and quantitative analysis of pharmaceutical products in accordance with FDA, cGMP and internal SOPs. The role involves hands-on analysis using HPLC, GC, UV-Vis and other methods, with a focus on method development and rigorous documentation.

Qualified candidates will hold a bachelor’s degree in chemistry and have 0–2 years of related experience, with a preference for knowledge of cGMPs.

Qualifications

  • Bachelor’s degree in chemistry or related science required.
  • 0–2 years of related experience preferred.
  • Knowledge of cGMPs and related compliance preferred.

Responsibilities

  • Prepare and analyze products to determine chemical and physical properties.
  • Confer with chemists and client personnel regarding procedures, results and reports.
  • Train to become proficient at assigned tasks and act as a subject matter expert.
  • Perform routine data generation and problem solving with minimal rework.
  • Work to ensure compliance with SOPs, cGMPs, and FDA regulations.
  • Ensure all work adheres to company, client and pharmacopeial methodologies.
  • Maintain equipment through system maintenance and calibrations as required.
  • Learn proper handling of hazardous waste per rules.
  • Document work clearly and organize records.
  • Follow safety rules and conduct periodic safety audits.

Skills

Organizational skills
Verbal communication
Technical documentation
Team player

Education

Bachelor’s degree in chemistry

Job description

BA Sciences is seeking a Chemist to conduct qualitative and quantitative analysis of pharmaceutical products in accordance with FDA, cGMP and internal SOPs. The role involves hands-on analysis using HPLC, GC, UV-Vis and other methods, with a focus on method development and rigorous documentation.

Qualified candidates will hold a bachelor’s degree in chemistry and have 0–2 years of related experience, with a preference for knowledge of cGMPs.

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