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Associate Scientist Analytical Development Jobs in Tennessee

This key role within Decision Science & Analytics will lead the ongoing development and execution of the Company's product shrink and damages forecasting and mitigation efforts. This role will work ...

This key role within Decision Science & Analytics will lead the ongoing development and execution of the Company's product shrink and damages forecasting and mitigation efforts. This role will work ...

Associate Director, Data Science

Knoxville, TN · On-site

$56K - $56K/yr

Why Join Tombras Analytics? Tombras Analytics sits at the cornerstone of Connecting Data ... You'll lead the strategy and development of proprietary tooling, work on brands with household ...

Tombras Analytics sits at the cornerstone of Connecting Data + Creativity for Business Results and ... You'll lead the strategy and development of proprietary tooling, work on brands with household ...

Senior Research Scientist

Oak Ridge, TN · On-site

$94K - $120K/yr

Ability to mentor scientists, engineers, and technical staff in detector physics, semiconductor process development, experimental methods, and performance analysis. * Strong scientific judgment ...

Senior Research Scientist

Oak Ridge, TN · On-site

$94K - $120K/yr

Ability to mentor scientists, engineers, and technical staff in detector physics, semiconductor process development, experimental methods, and performance analysis. * Strong scientific judgment ...

Ability to mentor scientists, engineers, and technical staff in detector physics, semiconductor process development, experimental methods, and performance analysis. * Strong scientific judgment ...

Showing results 21-40

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:

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.

Scientist - Development in Therapeutics Production & Quality

Socket.dev

Memphis, TN • On-site

$86 - $155/hr

Other

Posted 17 days ago


Key responsibilities

  • Design and implement process development experiments for upstream and downstream unit operations.

  • Support development, documentation, and reporting of experimental data related to manufacturing processes.

  • Coordinate project activities, execute processes, and support equipment maintenance and calibration.


Job description

Join our Team!

The Therapeutics Production and Quality department within our Good Manufacturing Practices (GMP) facility is looking for a Scientist - Development to design and implement process development experiments with minimal supervision including both upstream and downstream unit operations. In this role you will perform small scale cell culture experiments, set up and run bioreactors for culture of mammalian or bacterial cells, and optimize purification methods using various chromatography techniques. Experience in mammalian and bacterial cell culture, bioreactors, protein purification, plasmid DNA purification, tangential flow filtration and various other filtration techniques is preferred. You will generate purified plasmid DNA and gene therapy vectors including Lentiviral.

Job Responsibilities:

  • Coordinate multiple aspects of projects/processes within area (GMP/ECTL) with guidance, and execute processes (e.g., tech transfer & scale-up runs, HPLC/biologic assays, manufacturing of cellular therapeutics) utilizing appropriate techniques, equipment, and methods.
  • Provide inputs regarding revisions to SOPs and/or process flows within area.
  • Support development, documentation, and reporting of relevant experimental data (e.g., production batch records, HPLC reports, summary reports for manufacturing campaigns).
  • Monitor and document compliance with quality and regulatory requirements; and address deviations.
  • Support monitoring and stocking of supplies, and calibration, maintenance, troubleshooting, and purchase of equipment within area.
  • Instruct other staff in basic techniques, procedures, and systems within area (e.g., operations of cGMP equipment and control software).
  • Perform other duties as assigned to meet the goals and objectives of the department and institution.
  • Maintains regular and predictable attendance.

Minimum Education and/or Training:

  • Bachelor's degree required.
  • Master's OR PhD preferred.

Minimum Experience:

  • Minimum Requirement: Bachelor's degree with 7+ years experience in relevant scientific area (e.g., GMP: chemistry, biology, chemical engineering, analytical chemistry, biotechnology; ECTL: cellular biology, molecular biology, immunology, biochemistry).
  • Experience exception: 5+ years of experience in relevant area with Master's
  • Experience exception: 3+ years of experience in relevant area with PhD
  • Prior experience in relevant area to own domain (e.g., upstream/downstream cGMP experience, process development, HPLC/biological assays) strongly preferred.
  • Experience in lab and scientific project coordination, maintenance, and other research support activities preferred.

Compensation

In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $86,320 - $154,960 per year for the role of Scientist - Development in Therapeutics Production & Quality.

Explore our exceptional benefits!

St. Jude is an Equal Opportunity Employer

No Search Firms

St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

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