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Associate Scientist Analytical Development Jobs in Tennessee

GlycoData

Associate Applications Scientist

Kingsport, TN · On-site

$80 - $120/hr

Eastman Chemical Company is seeking an experienced Applications Development / Research Scientist to ... Design and analyze DOE and statistical studies to optimize formulations and process parameters.

St. Jude Children's Research Hospital

$65.52 - $114.40/hr

Perform separation, purification, and analytical characterization of amino acids. * Operate and ... Associate Scientist in Kalodimos Lab. Explore our exceptional benefits ! St. Jude is an Equal ...

Eastman

Associate Applications Scientist

Kingsport, TN · On-site

Description Eastman Chemical Company is seeking an experienced Applications Development / Research ... Design and analyze DOE and statistical studies to optimize formulations and process parameters.

Eastman

Associate Applications Scientist

Kingsport, TN · On-site

$80 - $120/hr

Description Eastman Chemical Company is seeking an experienced Applications Development / Research ... Design and analyze DOE and statistical studies to optimize formulations and process parameters.

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All JobsAssociate Scientist Analytical Development JobsAssociate Scientist Analytical Development Jobs in Tennessee

Associate Scientist Analytical Development information

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.

What are popular job titles related to Associate Scientist Analytical Development jobs in Tennessee?

For Associate Scientist Analytical Development jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Associate Scientist Analytical Development jobs in Tennessee look for?

The top searched job categories for Associate Scientist Analytical Development jobs in Tennessee are:

What cities in Tennessee are hiring for Associate Scientist Analytical Development jobs?

Cities in Tennessee with the most Associate Scientist Analytical Development job openings:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution.

Senior Scientist - Analytical Development

Augustbio

Nashville, TN • On-site

$120 - $150/hr

Other

Posted 18 days ago

Job description

Senior Scientist at August Bio will be responsible for leading complex research and development activities in the pharmaceutical field, including designing and executing laboratory experiments, analyzing data, and contributing to the development of new drug formulations, while ensuring adherence to all regulatory standards and company quality control procedures, often with a focus on analytical method development and validation for quality control testing of pharmaceutical products.

Key Responsibilities
  • Independently design and conduct laboratory experiments to support drug development projects, including formulation optimization, stability studies, and bioanalytical assays.
  • Analyze experimental data, interpret results, and prepare comprehensive reports to inform decision-making.
  • Collaborate with cross-functional teams (clinical, regulatory, manufacturing) to ensure seamless project execution.
  • Develop and validate sensitive and specific analytical methods for the quality control testing of pharmaceutical products using various techniques like HPLC, dissolution, and other relevant analytical methods.
  • Ensure analytical methods comply with regulatory requirements (cGMP) for accuracy, precision, specificity, and robustness.
  • Maintain detailed documentation of experimental procedures and results in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Conduct quality control checks on experimental data and ensure data integrity.
  • Proactively identify and address potential quality issues.
  • Provide technical guidance and mentorship to junior scientists on the team.
  • Contribute to the development of new scientific approaches and technologies.
Qualifications
  • Masters in Pharmaceutical Sciences, Chemistry, or a related field with significant experience in pharmaceutical development.
  • Extensive hands‑on experience with analytical techniques like HPLC and other relevant analytical methodologies.
  • Strong understanding of regulatory requirements (cGMP, GLP) and ability to apply them in laboratory practices.
  • Excellent problem‑solving skills and ability to work independently and as part of a team.
  • Proven track record of scientific publications and presentations at conferences.
Physical Requirements
  • Prolonged periods sitting at a desk and working on a computer.
  • Must be capable of wearing all appropriate PPE correctly during handling of hazardous substances.
  • Some work may require extended periods of time standing at a lab bench, cleanroom or stability chamber.
  • Must be visually capable of accurately measuring and reading volumes of solution in volumetric apparatus (e.g. accurately read meniscus).
  • Ability to lift, carry, push, or pull up to 40 lbs occasionally, and up to 30 lbs frequently. Two-person team lift or use of mechanical assist device is required for loads exceeding 50 lbs.
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