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Analytical Research And Development Scientist Jobs in Indiana

We also manufacture many specialty products to support validation and QC programs for analytical ... Manage product development projects, including directing the work of Scientists as appropriate.

Additionally, the R&D scientist will be involved in projects for qualification of raw materials, label compliance, product and ingredient testing, databases, analytical data, among others. The right ...

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... analyzing functions, APP Engineering needs to grow our Research and Development Department ... scientific trends by attending industry conferences such as the Georgia Tech University, Texas A&M ...

R&D Formulation Scientist

Columbus, IN · On-site

$27 - $30/hr

... Scientist to join our Research & Development team. The ideal candidate will have 3-5+ years of ... Write, review, and execute analytical and microbiological test methods. * Lead and support method ...

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Analytical Research And Development Scientist information

What are some common challenges analytical research and development scientists face when transitioning projects from the laboratory to full-scale production?

Analytical Research and Development Scientists often encounter challenges such as ensuring that analytical methods validated on a small scale remain robust and reliable during scale-up to production environments. Variability in raw materials, equipment differences, and stricter regulatory requirements can impact method performance and data integrity. Close collaboration with manufacturing, quality assurance, and regulatory teams is essential to address these challenges and ensure seamless technology transfer. Effective communication and thorough documentation help mitigate risks during this critical transition period.

What does an analytical research and development scientist do?

An Analytical Research and Development (R&D) Scientist is responsible for designing, conducting, and interpreting experiments to analyze the composition and quality of products, typically in industries such as pharmaceuticals, chemicals, or biotechnology. They develop and validate analytical methods to ensure products meet regulatory standards and specifications. Their work is crucial in supporting product development, quality control, and regulatory submissions, often collaborating with other scientists and departments. Analytical R&D Scientists also document their findings and may be involved in troubleshooting and improving existing analytical techniques.

What are the key skills and qualifications needed to thrive as an analytical research and development scientist?

To thrive as an Analytical Research and Development Scientist, you need a strong background in chemistry or related sciences, experience in laboratory research, and at least a bachelor's (often master's or PhD) degree in a relevant field. Proficiency in analytical instrumentation such as HPLC, GC, LC-MS, and familiarity with data analysis software and regulatory guidelines (like GLP/GMP) are typically required. Attention to detail, problem-solving abilities, and effective communication skills are crucial soft skills for success in this role. These competencies ensure accurate data generation, support innovation, and maintain compliance in developing and improving products or processes.

What is the difference between Analytical Research And Development Scientist vs Quality Control Analyst?

AspectAnalytical Research And Development ScientistQuality Control Analyst
CredentialsBachelor's or Master's in Chemistry, Biochemistry, or related fieldBachelor's in Chemistry, Biology, or related field
Work EnvironmentLaboratories focused on developing and optimizing analytical methodsQuality control labs performing routine testing of products
Employer & IndustryPharmaceutical, biotech, or chemical companiesManufacturing and production facilities in similar industries
Job FocusDeveloping new analytical techniques and methodsEnsuring product quality through testing and inspection

While both roles work in laboratory settings within the pharmaceutical and chemical industries, the Analytical Research And Development Scientist focuses on creating and improving analytical methods, whereas the Quality Control Analyst primarily tests products to ensure they meet quality standards.

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RESEARCH & DEVELOPMENT SCIENTIST (5360)

TECHNICAL RESOURCE MANAGEMENT LLC

Indianapolis, IN

Full-time

Posted 2 days ago

New


Job description

Research and Development Scientist

Position Overview: We are seeking a talented Research & Development Scientist to join our toxicology laboratory team in Indianapolis, IN. This position is responsible for the research, development, validation, and continuous improvement of testing methods used to detect drugs of abuse in urine and oral fluid specimens. This role works independently to design and execute method development studies across EMIT immunoassay and LC-MS/MS platforms, applying extraction techniques including liquid-liquid extraction, crash and shoot, and dilute and shoot. The R&D Scientist collaborates closely with the Scientific Director, Laboratory Manager, and Quality Assurance team to bring new methods into compliant, production-ready use and to troubleshoot and optimize existing assays.

Reports to: Scientific Director

Key Responsibilities:

Method Development & Validation

· Assay Development: Designs, develops, and validates new testing methods for drugs of abuse in urine and oral fluid specimens using EMIT immunoassay and LC-MS/MS platforms.

• Extraction Techniques: Applies and refines extraction methods, including liquid-liquid extraction, crash and shoot, and dilute and shoot, in support of method development.

• Instrumentation Expertise: Applies working knowledge of Agilent and Waters LC-MS/MS platforms to method development and troubleshooting.

• Validation Studies: Designs and executes validation studies (e.g., precision, accuracy, linearity, specificity, stability) to support new and modified test methods, documenting results in accordance with regulatory standards.

Process Improvement & Troubleshooting

· Assay Optimization: Continuously evaluates existing methods to identify opportunities for improved sensitivity, specificity, turnaround time, or cost efficiency.

· Technical Troubleshooting: Serves as a technical resource to production laboratory staff, investigating and resolving instrument or method-related issues that affect testing quality or turnaround time.

· Root Cause Analysis: Leads root cause investigations for method-related failures, QC exceptions, or unexpected results, and develops corrective/preventive action plans.

Documentation & Compliance

· SOP Development: Authors and maintains Standard Operating Procedures (SOPs) for new and existing test methods in coordination with the Scientific Director and Quality Assurance team.

· Regulatory Compliance: Ensures all method development and validation work complies with applicable regulatory and accreditation standards (e.g., CLIA, CAP- FDT).

· Technical Documentation: Maintains detailed records of experiments, validation studies, and method changes to support audits, inspections, and litigation requests as needed.

Collaboration & Communication

· Cross-Functional Coordination: Works closely with the Scientific Director, Laboratory Manager, and Certifying Scientists/Supervisors to transition validated methods into routine production use.

· Technical Guidance: Provides technical training and guidance to laboratory staff on new methods, instrumentation, or procedural changes.

• Reporting: Prepares technical reports and presentations summarizing method development and validation findings for internal stakeholders.

• New Testing Opportunities: Works with the Scientific Director to evaluate new testing opportunities based on the needs of the company and clients.

Qualifications:

Education & Experience:

· Education: Bachelor's degree in Chemistry, Biochemistry, Toxicology, Forensic Science, or a related science field required.

· Experience: 3+ years of laboratory experience in a toxicology, forensic, or clinical laboratory setting, including hands-on experience with LC-MS/MS method development and validation.

Knowledge, Skills, and Abilities:

· Instrumentation Proficiency: Hands-on experience with Agilent and/or Waters LC-MS/MS platforms strongly preferred; experience with EMIT immunoassay technology required.

· Extraction Techniques: Demonstrated experience with liquid-liquid extraction, crash and shoot, and dilute and shoot sample preparation methods.

· Analytical Skills: Strong understanding of analytical chemistry principles, method validation protocols, and troubleshooting techniques.

· Regulatory Knowledge: Familiarity with CLIA, CAP- FDT, and other relevant regulatory/accreditation standards.

· Communication Skills: Strong written and verbal communication skills, with the ability to author technical documentation and present findings clearly.

· Independence & Initiative: Ability to work independently, manage multiple projects, and drive method development work from concept through validation.

Physical & Environmental Requirements:

· Ability to move around the lab, perform standing tasks, and occasionally lift light to moderate weights.

· Work in a laboratory setting with potential exposure to laboratory chemicals, equipment, and other operational conditions. #LAB123