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Associate Scientist Analytical Development Jobs in Texas

Abbott

Associate Scientist II

Irving, TX · On-site

Associate Scientist II Location: Irving, TX Duration: 12 Months 100% Onsite Job Summary The ... analysis tools. * Previous experience supporting clinical chemistry product development or ...

SLR Consulting

Associate Scientist

Houston, TX · On-site

$90 - $130/hr

Excellent analytical, organizational, and multitasking abilities* Demonstrated experience solving ... Mentor junior staff and foster skill development within the team* Learn and apply compliance ...

SLR Consulting Limited

Associate Scientist

Houston, TX · On-site

Excellent analytical, organizational, and multitasking abilities * Demonstrated experience solving ... Mentor junior staff and foster skill development within the team * Learn and apply compliance ...

Slrconsulting

Associate Scientist

Houston, TX

Excellent analytical, organizational, and multitasking abilities * Demonstrated experience solving ... Mentor junior staff and foster skill development within the team * Learn and apply compliance ...

Nulixir Inc.

Associate Scientist

Austin, TX · On-site

The firm's founder has extensive experience in the development of nanocarriers for cancer ... Associate Scientist reporting to our Director of Product. This is not just a job; it's an ...

DiaSorin

Associate Scientist II

Austin, TX · On-site

... and development of assays based on Luminex's technology platform and chemistries. Handles ... Data analysis and technical writing aptitude. (Medium proficiency) What we offer The hiring range ...

DiaSorin

Associate Scientist II

Austin, TX

... and development of assays based on Luminex's technology platform and chemistries. Handles ... Data analysis and technical writing aptitude. (Medium proficiency) What we offer The hiring range ...

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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 Texas?

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

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

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

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

Cities in Texas 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 Texas as of August 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% In-person job distribution.

Analytical Development Scientist I

Sovereign Pharmaceuticals

Fort Worth, TX • On-site

Full-time

Re-posted 16 days ago

Job description

summary / objective
Support Sovereign’s analytical development activities to achieve successful design, filing, transfer and launch of 505(b)2, ANDA and OTC products.
essential functions
· Perform release and stability testing for raw materials and drug products
· Execute method transfers and method equivalency studies
· Conduct method validation experiments as per written protocols
· Performs characterization of physical and chemical characteristics of drug product and raw materials.
· Peer review laboratory notebooks, data, protocols and reports
· Understands applicable cGMP, DEA regulations and Quality Procedures
· Performs other tasks as assigned.
work environment
This job operates in a professional office and laboratory environment. This role routinely uses standard office equipment such as computers, phones, and copiers. The employee is occasionally exposed to toxic and/ or caustic chemicals such as Sodium Hydroxide, Hydrochloric Acid, Acetonitrile, Methanol, and other chemical solutions necessary in analytical chemistry.
physical demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must regularly lift and/ or move up to 50 pounds. Specific vision abilities required by this position include close vision, color vision and the ability to adjust focus. While performing the duties of this job, the employee is regularly required to stand, walk, sit and talk or hear. The employee is occasionally required to climb or balance, stoop, kneel, crouch, crawl and smell.
position type/expected hours of work This is a full-time position. Days and hours of work are Monday through Friday but extended (earlier or later) work times or weekend work may be required.
required education and experience
· Advanced degree with Chemistry background, Masters preferred
· 2-5 years experience in pharmaceutical laboratory
· Operation of HPLC and efficient with Empower 3 Software
· Compendial/Non-compendial testing of raw materials
· Adhere to all laboratory requirements in accordance with SOPs and regulatory practices such as GMPs, GDPs, GLPs, and OSHA regulations.
· Understanding of Analytical Chemistry including but not limited to the following techniques and how to utilize them, as needed, for projects, both simple and complicated, as assigned:
o HPLC
o Dissolution
o UV/Vis
o FTIR
o Sample Preparation Techniques
o GC
o Titration/electrode chemistry
o Others as appropriate
· Effective communication skills, written and verbal
· Demonstrate project management skills
· Organizational and interpersonal skills
· Ability to innovate new ideas
preferred education and experience
· Advanced degree with Chemistry background, Masters preferred
· 2-5 years experience in pharmaceutical laboratory
· Self Starter
· Organized
· Dependable
· Goal Oriented
· Ability to handle multiple projects
work authorization/security clearance (if applicable)
Authorized to work in the U.S.

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