ZipRecruiter

Log In

1

Quality Scientist Jobs (NOW HIRING)

Orano

Quality Scientist

Plano, TX · On-site

The Quality Scientist partners closely with QC, Analytical Development, Manufacturing, and QA teams. Using strong scientific judgment and GMP expertise, this position leads investigations, evaluates ...

Actalent

Quality Scientist II

Dublin, OH · On-site

Quality Scientist II INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW! The Quality ...

Actalent

Quality Scientist II

Dublin, OH · On-site

Quality Scientist II INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW! The Quality ...

Arcadis

Air Quality Scientist

Houston, TX · On-site +1

Arcadis is seeking an Air Quality Scientist to join our Integrated Sustainability and Compliance (ISC) team, in a Texas office such as Austin, Dallas, or Houston. This will be a hybrid role ...

Abaxis

Quality Scientist I

Charles City, IA

The individual will be a member of the animal testing division in the Quality Control department ... EDUCATION AND EXPERIENCE : * 2 to 4 Year Degree (science background preferred) and/or 0-3 years of ...

Zoetis, Inc.

Quality Scientist I

Charles City, IA · On-site

The individual will be a member of the animal testing division in the Quality Control department ... EDUCATION AND EXPERIENCE : * 2 to 4 Year Degree (science background preferred) and/or 0-3 years of ...

next page

Showing results 1-20

All JobsQuality Scientist Jobs

Quality Scientist information

See salary details

$17

$34

$61

How much do quality scientist jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for quality scientist in the United States is $34.52, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $39.66 per hour, depending on experience, location, and employer.

What are Quality Scientists?

Quality Scientists are professionals who ensure that products, materials, and processes meet established quality standards and regulatory requirements. They design and implement testing procedures, analyze data to detect deviations, and collaborate with other departments to improve quality systems. Quality Scientists often work in industries such as pharmaceuticals, biotechnology, food production, and manufacturing. Their work helps maintain product safety, efficacy, and compliance, playing a vital role in protecting consumers and supporting organizational reputation.

What are the key skills and qualifications needed to thrive as a Quality Scientist, and why are they important?

To thrive as a Quality Scientist, you need a strong background in chemistry, biology, or a related field, typically supported by a relevant degree and experience in quality assurance or control. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and regulatory standards such as ISO is essential. Attention to detail, analytical thinking, and effective communication set top performers apart in this role. These skills are crucial to ensure product safety, regulatory compliance, and continuous improvement in laboratory and manufacturing environments.

How does a Quality Scientist typically collaborate with other departments to ensure product standards are met?

Quality Scientists regularly work alongside teams in manufacturing, research and development, and regulatory affairs to uphold product quality standards. They often coordinate with production staff to implement testing protocols, communicate findings to R&D for process improvements, and ensure compliance with industry regulations by working closely with regulatory teams. This cross-functional collaboration is essential for identifying potential issues early and maintaining consistent product quality throughout the development and manufacturing process.

What is the difference between Quality Scientist vs Quality Assurance Specialist?

AspectQuality Scientist

CredentialsBachelor's or higher in life sciences, chemistry, or related fields; often requires experience in research or development
Work EnvironmentLaboratories, R&D departments, product development teams
Employer & IndustryPharmaceutical, biotech, food, and consumer goods companies
Common Search & ComparisonOften compared for roles in product quality and compliance

While both roles focus on ensuring product quality, a Quality Scientist primarily conducts research, development, and testing to improve products. In contrast, a Quality Assurance Specialist focuses on implementing and maintaining quality systems, inspections, and compliance processes. Both roles are essential in manufacturing and R&D environments, but they differ in daily responsibilities and focus areas.

More about Quality Scientist jobs
What cities are hiring for Quality Scientist jobs? Cities with the most Quality Scientist job openings:
What states have the most Quality Scientist jobs? States with the most job openings for Quality Scientist jobs include:
What job categories do people searching Quality Scientist jobs look for? The top searched job categories for Quality Scientist jobs are:
Quality Scientist jobs near you

Quality Scientist

Orano

Plano, TX • On-site

Full-time

Posted 3 days ago

Job description

Description
Orano Med Theranostics
Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.
Orano Med LLC has opening for Quality Scientist in Plano, TX.
This role ensures the integrity, reliability, and regulatory compliance of analytical methods and their transfers used for drug product testing from early development through Phase 2 clinical manufacturing. The Quality Scientist partners closely with QC, Analytical Development, Manufacturing, and QA teams. Using strong scientific judgment and GMP expertise, this position leads investigations, evaluates analytical trends, drives effective CAPAs, and ensures method qualification, validation, and transfer activities meet FDA, EMA, and global regulatory expectations. Success requires exceptional analytical acumen, meticulous attention to detail, and the ability to translate complex laboratory and process data into compliant, practical solutions that protect product quality and patient safety.
Key Responsibilities
  • Perform thorough technical review of QC analytical data, including raw data, chromatograms, calculations, audit trails, and reports to verify accuracy, data integrity, and method compliance while identifying trends.
  • Lead and support analytical method qualification, validation, and transfer activities, including protocol review, data evaluation, receiving site alignment, and adherence to ICH Q2/Q14, FDA, and EMA guidelines.
  • Drive continuous improvement of the analytical qualification/validation program through data trending, method performance monitoring, and initiatives to enhance robustness and reduce variability.
  • Conduct scientifically sound investigations of analytical deviations, OOS/OOT results, and nonconformances, ensuring robust root cause analysis and effective CAPA implementation.
  • Provide technical review and approval of method transfer packages, validation documents, and associated data to ensure regulatory and internal compliance.
  • Assess manufacturing processes, method performance, and R&D recommendations to identify risks, propose improvements, and support method optimization and lifecycle management.
  • Execute complex quality and analytical tasks to deliver consistent, high-quality data, methods, and processes across the product development lifecycle.
  • Perform additional duties as assigned to advance quality system maturity, analytical readiness, and regulatory compliance.

Requirements
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.
Minimum Qualifications
  • Bachelor's of Science (or higher) in Chemistry or other related field
  • 7+ years experience in Pharmaceuticals
  • 5+ years experience as a QC analyst or Method Development

Preferred Skills & Competencies
  • Strong experience performing technical review of Analytical Data
  • Experience writing & reviewing SOPs, Protocols, Technical Reports and other associated GMP documentation
  • In-depth knowledge of cGMP, GLP, FDA/EMA regulations, ICH guidelines, USP/EP pharmacopeial methods, and data integrity principles.
  • Proficient in Microsoft Office, Excel, and Power Point
  • Excellent technical writing and verbal communication skills.
  • Strong organization skills and attention to detail.
  • Able to easily switch between multiple ongoing projects, adjusting priorities based on business needs.

Apply