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Qc Associate Scientist Jobs (NOW HIRING)

Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 Months Job Type: Temporary Assignment Work Type: Onsite Summary With limited supervision, the QC ...

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

High School Diploma with 6+ years, Associate Degree with 4+ years, or Bachelor's Degree in a science or engineering field with 2+ years of cGMP experience * Prior Quality Control experience preferred

Maintain records and QC lab environment to comply with cGMP, OP and regulatory requirements ... Associates or Bachelor's Degree in Science or Life Science discipline. Founded in 2010 and ...

Quality Control Associate

Manhattan, NY · On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

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he Quality Control Associate plays a critical role within the Quality Team, performing routine quality checks on vitamin gummies, tablets, capsules, powders, and IV products . This position focuses ...

Quality Control Associate

New York, NY · On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

K2 is seeking a Quality Control Associate to support our clinics out of either Maitland or Winter Garden , FL . This position is hybrid with support needed one to two days out of the week at the ...

The Role As a Quality Control (QC) Associate at CookUnity, you play a key role in ensuring the quality, accuracy, and presentation of meals throughout the production process. You'll support the QC ...

We are currently seeking a detail-oriented and proficient individual to join our team as a Quality Control Associate in the Pre-Press Department. In this role, you will play a crucial part in ...

Quality Control Associate

Manhattan, NY · On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

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Qc Associate Scientist information

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$18

$35

$57

How much do qc associate scientist jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for qc associate scientist in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

What is a QC Associate Scientist?

QC Associate Scientists are professionals who work in quality control laboratories, primarily within the pharmaceutical, biotechnology, or related industries. They are responsible for conducting tests and analyses on raw materials, in-process materials, and finished products to ensure they meet established quality standards and regulatory requirements. Their duties often include preparing samples, operating laboratory equipment, documenting results, and assisting in method development and validation. QC Associate Scientists play a crucial role in maintaining product safety and integrity by identifying deviations and supporting investigations. They usually work under the supervision of senior scientists or QC managers.

What are the key skills and qualifications needed to thrive as a QC Associate Scientist?

To thrive as a QC Associate Scientist, you need a strong background in chemistry, biology, or a related field, typically with a bachelor's or master's degree, and experience in laboratory testing and data analysis. Familiarity with analytical instruments (such as HPLC, GC, and PCR), laboratory information management systems (LIMS), and GMP/GLP regulations is essential. Attention to detail, problem-solving abilities, and effective communication skills help ensure accuracy and collaboration within quality control teams. These competencies are vital for maintaining product quality, regulatory compliance, and the integrity of scientific results.

How does a QC Associate Scientist typically collaborate with other teams within a laboratory setting?

As a QC Associate Scientist, you will often work closely with cross-functional teams such as manufacturing, quality assurance, and research and development. Collaboration involves communicating test results, resolving discrepancies, and ensuring that all products meet regulatory and internal quality standards. Regular meetings and data sharing are common, and you may also participate in investigations or troubleshooting efforts when deviations occur. These interactions are key to maintaining workflow efficiency and upholding product integrity.

What is the difference between Qc Associate Scientist vs Qc Analyst?

AspectQc Associate ScientistQc Analyst
Required CredentialsBachelor's degree in Life Sciences, Chemistry, or related field; often some laboratory experienceBachelor's degree in Science; entry-level to mid-level laboratory experience
Work EnvironmentLaboratories within pharmaceutical, biotech, or manufacturing companiesQuality control labs in similar industries, focusing on testing and analysis
Employer & Industry UsageCommonly used in biotech and pharmaceutical industries for product testing and validationWidely used in manufacturing and quality assurance departments across industries

The Qc Associate Scientist and Qc Analyst roles share similar educational backgrounds and work environments, primarily focusing on laboratory testing within the pharmaceutical and biotech sectors. The Associate Scientist often involves more scientific analysis and method development, while the Qc Analyst emphasizes routine testing and data recording. Both roles are essential for maintaining product quality and compliance.

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Infographic showing various Qc Associate Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $74,723 per year, or $35.9 per hour.

Quality Control Scientist

Vacaville, CA • On-site

TekWissen LLC
Recruiting and Staffing Services • 501 - 1,000 employees

$20 - $25/hr

Temporary

Re-posted 4 days ago


Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       QC Associate I / Quality Control Scientist
Location:       Vacaville, CA - 95688
Duration:       6 Months
Job Type:       Temporary Assignment     
Work Type:   Onsite

Summary
 
With limited supervision, the QC Associate I / Quality Control Scientist is responsible for performing direct materials testing in compliance with cGMP regulations. The role involves executing laboratory testing, reviewing and trending data, supporting investigations (OOS, OOT, OOE), and contributing to laboratory operations and quality objectives. The position works closely with Quality Control leadership to meet departmental and organizational goals.

Responsibilities

  • Perform basic to moderately complex laboratory testing in compliance with GMP requirements
  • Review, analyze, and assess test data against established acceptance criteria
  • Conduct technical review of peer-generated data
  • Perform trend analysis and assist in establishing limits
  • Identify discrepancies and support quality investigations and CAPA initiatives
  • Troubleshoot technical and testing-related issues
  • Identify gaps in systems, procedures, and laboratory practices
  • Participate in assay transfer, assay validation, and method-related activities
  • Perform equipment qualification, calibration, and routine maintenance
  • Prepare and maintain standards, controls, stocks, cultures, and reagents per procedures
  • Ensure GMP compliance across laboratory operations
  • Support internal and external audits and regulatory inspections
  • Coordinate with internal customers to support multi-site operations
  • Meet assigned schedules, timelines, and deadlines (95% on-time performance expectation)
  • Participate in or lead team projects, process improvements, and continuous improvement initiatives
  • Write protocols, reports, and technical documentation under limited supervision
  • Provide and receive training as required
  • Perform additional duties as assigned to support Quality activities
Required Skills
  • Bachelor’s degree (B.S./B.A.) in a relevant scientific discipline with 1–3 years of industry experience OR
  • Master’s degree with at least 1 year of relevant experience
  • Experience in the pharmaceutical or biopharmaceutical industry
  • Hands-on experience with analytical and/or biological testing procedures
  • Strong understanding of cGMP regulations and quality systems
  • Experience with OOS, OOT, and OOE investigations
  • Exposure to assay transfer, assay validation, and method lifecycle activities
  • Experience supporting regulatory inspections (FDA, EMA, etc.)
  • Familiarity with trend analysis and data integrity practices
  • Prior involvement in process improvement or cross-functional projects
  • Experience working in multi-site or global operational environments
  • Ability to apply scientific principles, theories, and techniques in a QC environment
  • Strong verbal and written communication skills
  • Sound judgment, analytical thinking, and problem-solving abilities
  • Ability to work independently with limited supervision and manage short-term priorities
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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