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Analytical Method Development Validation Chemist Jobs

Phoenix Tailings

9.6. R&D Analytical Chemist

Woburn, MA · On-site

$70K - $90K/yr

Opportunity Overview Phoenix Tailings is looking for an R&D Analytical Chemist to drive the ... Familiarity with analytical method development, validation, or adaptation for non‑routine samples.

Techtrueup

Quality Control Chemist II

Duluth, GA · On-site

Quality Control Chemist II Location: Johns Creek, GA - Onsite Duration: 12 months, with potential ... The successful candidate will be responsible for analytical method development, validation and ...

Techtrueup

Quality Control Chemist II

Duluth, GA · On-site

Quality Control Chemist II Location: Johns Creek, GA - Onsite Duration: 12 months, with potential ... The successful candidate will be responsible for analytical method development, validation and ...

Merck Group

Analytical Chemist

Branchburg, NJ · On-site

$55K - $165K/yr

Develop and validate analytical methods for CoA parameters and transfer operating procedures to ... Work closely with R&D, production, quality, and commercial teams to ensure rapid delivery of new ...

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How much do analytical method development validation chemist jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for analytical method development validation chemist in the United States is $31.50, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $36.06 per hour, depending on experience, location, and employer.

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Infographic showing various Analytical Method Development Validation Chemist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $65,525 per year, or $31.5 per hour.

Analytical Chemistry Specialist

Bangor, PA • On-site

Biospectra Inc
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Biospectra Incexternal

Full-time

Posted 24 days ago

Job description

Job Overview:


This position plays an important role in BioSpectra’s Laboratory Services department. The position is responsible for all stages of method implementation from method development and method validation to routine analysis.   The Analytical Chemistry Specialist will be responsible for instrumentation development work, which includes getting new instrumentation online and operational while streamlining existing methods. 

This position would be ideal for an analytical chemistry professional who is seeking a challenging opportunity with a growing Bio-Pharmaceutical Company.

Key Responsibilities:

  • Laboratory Instrumentation: 
    1. Responsible for operating complex laboratory instrumentation, including HPLC, UPLC, ICP-MS, ICP-OES, GC-MS, GC-FID, IC and SEM. 
    2. Maintain and troubleshoot issues related to complex instrumentation.
  • Inventory Management: Maintain: Maintain inventory and storage of instrumentation equipment and accessories.
  • Method Development & Validation:
    1. Assist in development of method feasibility for new products and streamline methods for existing products.
    2. Assist in method validation protocol generation, executing protocols, providing peer review and analysis of data.
    3. Assist in report generation regarding instrumentation.
  • Out of Specification Investigations: Assist in out-of-specification (OOS) result investigations by processing/interpreting data, conducting analysis and evaluating instrumentation.
  • Instrumentation Analytical Method Expertise: Function as an analytical subject matter expert for instrument analytical methods.
  • Analyst Training: Train QC Analysts to perform analysis on complex instrumentation.
  • Organic Impurity Analysis: Perform organic impurity analysis to support regulatory submissions.
  • Reference Standards: Source and qualify, when applicable, reference standards for analysis.
  • Routine Testing and Analysis: Perform analysis and review of routine instrument testing.

Skills & Qualifications:

  • Education: Bachelor's degree in Science or related field, and/or commensurate experience.
  • Experience: 
    1. A minimum of one to three years of experience in a quality control and/or cGMP laboratory, with demonstrated knowledge and experience operating LC, ICP and GC instrumentation in a GMP laboratory.
    2. Experience in the pharmaceutical or related industry in a laboratory setting, with knowledge of cGMP and related compliance regulations.
  • Skills & Capabilities: The ideal candidate will have demonstrated the following abilities:

    • Must be able to perform data analysis, complex analytical calculations and statistical analysis

    • Must be able to train QA Analysts on instrument analysis

    • Must have prior experience writing analytical protocols and reports

    • Must have prior experience performing organic impurity analysis