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Associate Scientist Analytical Development Jobs in Edmond, OK

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Associate Scientist Analytical Development information

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$16

$32

$51

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

As of Sep 3, 2026, the average hourly pay for associate scientist analytical development in Edmond, OK is $32.46, according to ZipRecruiter salary data. Most workers in this role earn between $25.19 and $36.92 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.

What are popular job titles related to Associate Scientist Analytical Development jobs in Edmond, OK?

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

What job categories do people searching Associate Scientist Analytical Development jobs in Edmond, OK look for?

The top searched job categories for Associate Scientist Analytical Development jobs in Edmond, OK are:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Edmond, OK as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $67,513 per year, or $32.5 per hour.

MSAT Senior Scientist

Cytovance Biologics Inc

Oklahoma City, OK • On-site

$84K - $116K/yr

Full-time

Posted 19 days ago

Job description

Position Summary

This role serves as an independent technical leader responsible for technology transfer, process scale-up, manufacturing support, process troubleshooting, and continuous improvement for commercial and clinical biopharmaceutical manufacturing. The individual will lead cross-functional activities from process transfer through GMP manufacturing while ensuring technical rigor, regulatory compliance, and successful execution.

Essential Responsibilities

· Lead technology transfer from clients and internal Process Development into GMP manufacturing.

· Author comprehensive Technology Transfer Protocols that provide sufficient technical detail for manufacturing batch record development.

· Develop process descriptions, manufacturing instructions, engineering calculations, and scale-up strategies.

· Perform process scale-up calculations for upstream and downstream operations and select scientifically justified scale-up parameters.

· Identify technical risks associated with scale-up and develop mitigation strategies.

· Generate, review, and approve Bills of Materials (BOMs); ensure technical accuracy because BOMs are provided to clients for approval and drive project cost.

· Support batch record development and manufacturing execution.

· Provide on-floor manufacturing support during engineering, clinical, PPQ, and commercial campaigns.

· Lead deviation, OOS, and OOT investigations to scientifically determine root causes and implement effective CAPAs.

· Support change controls, process validation, process characterization, comparability studies, and continuous improvement.

· Serve as technical interface with Process Development, Manufacturing, QC, QA, Facilities, Supply Chain, Project Management, and clients.

· Mentor junior engineers/scientists and provide technical leadership.

Technical Expertise

· Strong knowledge of upstream cell culture and/or microbial fermentation and downstream purification; downstream expertise preferred.

· Deep understanding of process scale-up principles including mixing, oxygen transfer, chromatography, filtration (terminal, viral, depth), UF/DF, and centrifugation.

· Experience supporting GMP manufacturing and MSAT workflows.

· Knowledge of process validation, process characterization, statistical analysis, and risk management.

· Experience preparing technical reports, protocols, investigations, and client-facing documentation.

Experience with Some of Root Cause Analysis & Investigation Tools

· 5 Whys

· Fishbone (Ishikawa/5M or 6M) Diagram

· Fault Tree Analysis (FTA)

· Failure Modes and Effects Analysis (FMEA)

· Pareto Analysis

· Control Charts (SPC)

· Trend Analysis

· Process Capability Analysis

· Hypothesis Testing (t-test, ANOVA, chi-square as appropriate)

· Regression and Correlation Analysis

· Scatter Plots

· Histograms

Qualifications

· BS, MS, or PhD in Chemical Engineering, Biochemical Engineering, Bioengineering, Biochemistry, Biology, Microbiology, or related discipline.

· Minimum 10 years of biopharmaceutical industry experience with 5 years in MSAT

· Demonstrated experience in MSAT, technology transfer, scale-up, and manufacturing support.

· Ability to independently lead technical investigations and make sound scientific decisions.

· Excellent technical writing skills for protocols, reports, and investigations.

· Strong project management and organizational skills.

Leadership & Interpersonal Competencies

· Excellent communication and presentation skills.

· Build trust across cross-functional teams.

· Professional, collaborative, and customer-focused.

· Able to influence without direct authority.

· Comfortable interacting with clients and senior management.

· Strong analytical thinking and sound technical judgment.