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How much do associate scientist analytical development jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for associate scientist analytical development in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

What does an associate scientist analytical development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What are some common challenges an associate scientist analytical development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What are the key skills and qualifications needed to thrive as an associate scientist analytical development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

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Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $74,723 per year, or $35.9 per hour.

Senior Associate Scientist (Contract), Polysaccharide Analytical Development

GlycoData

San Carlos, CA • On-site

$80 - $100/hr

Other

Posted 19 days ago

Job description

Senior Associate Scientist (Contract), Polysaccharide Analytical Development – Vaxcyte

Posted on: June 04, 2026

Description:

We are seeking a highly motivated and detail-oriented Senior Associate Scientist (Contract) to join our Polysaccharide team. Primary responsibility for the incumbent will be to support analytical testing and characterization of polysaccharide-based drug candidates. This individual will execute and optimize a variety of biochemical and chromatographic assays, contribute to method development initiatives, and ensure high-quality data generation in support of research and development programs.

Essential Functions:
  • Perform in-house assays for polysaccharide manufacturing, including in-process testing, process development and process characterization study sample analysis, including:
  • Spectrophotometric-based assays (e.g., UV/Vis, Lowry, PicoGreen, Anthrone, etc.)
  • Metabolite Analysis (e.g. sugars)
  • LC-MS-based assay
  • Prepare samples, reagents, standards, and controls according to established protocols.
  • Troubleshoot instrumentation and assay performance issues to ensure reliable data output.

Method Development & Optimization

  • Assist in developing, qualifying, and optimizing analytical methods for sample preparation, testing, and characterization.
  • Support method transfer, robustness evaluation, and documentation updates.
  • Proactively recommend improvements to increase assay sensitivity, reproducibility, and throughput.

Data Analysis & Reporting

  • Utilize data analysis software platforms such as Empower and Chromeleon for HPLC data acquisition and analysis, and SoftMax Pro for MSD and spectrophotometric assay data analysis.
  • Analyze, interpret, and summarize experimental data clearly and concisely.
  • Prepare technical summaries and present findings to cross-functional teams (e.g., R&D, CMC, Quality).

Compliance & Documentation

  • Maintain meticulous laboratory notebooks and electronic records in compliance with internal SOPs and laboratory standards.
  • Ensure data integrity and adherence to applicable regulatory guidelines (e.g., GLP/GMP where applicable).
  • Participate in audits, documentation reviews, and quality initiatives as needed.
  • Collaborate effectively with scientists across disciplines to support program milestones.
  • Demonstrate eagerness to learn new analytical techniques and scientific concepts.
  • Integrate best laboratory practices and contribute to a culture of operational excellence.
Requirements:
  • MSc in Chemistry/Biochemistry, Biotechnology, or similar degree with a minimum of 3 years of relevant industry experience, or BSc with a minimum of 5 years of relevant industry experience.
  • Hands-on experience with HPLC systems and carbohydrate or polysaccharide analysis.
  • Experience with HPAEC-PAD is preferred.
  • Experience with LC-MS/MS is a plus.
  • Experience with Empower and/or Chromeleon software.
  • Familiarity with biochemical assays (ELISA, colorimetric, fluorescence-based assays).
  • Experience working with polysaccharides, biologics, or complex drug substances.
  • Experience in in-process monitoring and testing for process-related impurities.
  • Knowledge of regulatory expectations for analytical documentation.
  • Experience supporting CMC, process development, or analytical development programs.
  • Strong organizational skills and attention to detail.
  • Excellent written and verbal communication skills.
  • Strong analytical and problem-solving skills.
  • High attention to data accuracy and reproducibility.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Collaborative team player with proactive communication style.

Reports to: Senior Scientist, Polysaccharide Analytical Development

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