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Senior Quality Control Associate Jobs (NOW HIRING)

Astrix Inc

Sr. QC Associate

Fremont, CA · On-site

The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Title: Sr. Quality Control Associate (Contract ...

Twist Bioscience

QC Associate - Temp

Portland, OR · On-site

... of senior QC staff. * Perform routine QC release testing and data review using established ... QC Associate II or above. * Perform raw material incoming inspections based on established ...

Twist Bioscience

QC Associate - Temp

Portland, OR · On-site

... of senior QC staff. * Perform routine QC release testing and data review using established ... QC Associate II or above. * Perform raw material incoming inspections based on established ...

Flux Resources

QC Associate

Ashburn, VA · On-site

$70 - $100/hr

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning ... Develop site- specific QC Programs for small to mid-level projects and submit to the QC Senior ...

Flux

QC Associate

Ashburn, VA · On-site

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning ... Develop site-specific QC Programs for small to mid-level projects and submit to the QC Senior ...

APN Software Services Inc

QC Associate

Tucson, AZ · On-site

Job title: QC Associate Duration: 12 months Location: Tucson, AZ The Quality Control Associate ... senior team members. Responsibilities ● Perform inspection and testing of raw materials, in ...

Flux

QC Associate

Richmond, VA · On-site

The purpose of Quality Control Associate is to update and coordinate the planning, implementation ... Develop site-specific QC Programs for small to mid-level projects and submit to the QC Senior ...

Grupo Canela Pvt Ltd

QC Associate

Pico Rivera, CA

$16 - $18/hr

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.

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Senior Quality Control Associate information

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How much do senior quality control associate jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for senior quality control associate in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.

What does a senior quality control associate do?

A Senior Quality Control Associate is responsible for overseeing and performing quality control tests on products or materials to ensure they meet company and regulatory standards. They analyze test data, identify trends or deviations, and help implement corrective actions when issues are found. Additionally, they may mentor junior team members, assist in developing testing protocols, and collaborate with other departments to resolve quality concerns. Their work is essential in maintaining product consistency, safety, and compliance within the organization.

What are the key skills and qualifications needed to thrive as a senior quality control associate?

To thrive as a Senior Quality Control Associate, you need a strong background in analytical testing, quality assurance principles, and relevant scientific education, often with a bachelor’s degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and regulatory compliance requirements is typically expected, along with proficiency in using laboratory instruments. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for excelling in this role. These competencies ensure the reliability of product quality, support regulatory compliance, and contribute to efficient cross-functional collaboration within the organization.

What are some typical challenges senior quality control associates face when overseeing multiple projects simultaneously?

Senior Quality Control Associates often manage several projects at once, which can present challenges such as balancing competing deadlines, ensuring consistent application of quality standards, and effectively communicating with cross-functional teams. Staying organized and prioritizing tasks is essential to prevent bottlenecks and maintain high-quality deliverables. Additionally, adapting quickly to changes in project scope or regulatory requirements is a key part of the role, as is mentoring junior team members to uphold best practices.

What is the difference between Senior Quality Control Associate vs Quality Control Associate?

AspectSenior Quality Control AssociateQuality Control Associate
Required CredentialsBachelor's degree, relevant certifications (e.g., CQE)Bachelor's degree often preferred, certifications optional
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or production settings
Employer & Industry UsagePharmaceuticals, biotech, manufacturing companiesPharmaceuticals, biotech, manufacturing companies
Job ResponsibilitiesOversees testing, reviews quality data, mentors junior staffPerforms testing, documents results, supports quality checks

The main difference between a Senior Quality Control Associate and a Quality Control Associate lies in experience, responsibilities, and leadership. Senior roles typically involve overseeing testing processes, mentoring staff, and ensuring compliance, while associate roles focus on executing tests and documenting results. Both positions are vital in maintaining product quality in industries like pharmaceuticals and manufacturing.

What cities are hiring for Senior Quality Control Associate jobs?

Cities with the most Senior Quality Control Associate job openings:

What states have the most Senior Quality Control Associate jobs?

States with the most job openings for Senior Quality Control Associate jobs include:

Infographic showing various Senior Quality Control Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $52,962 per year, or $25.5 per hour.

Sr. QC Associate

Astrix Inc

Fremont, CA • On-site

Full-time

Re-posted 8 days ago

Job description

Pay Rate Low: 32 | Pay Rate High: 34
Our client is a global, research-driven pharmaceutical manufacturer focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference!
Title: Sr. Quality Control Associate (Contract)
Location: Alameda County, CA
Schedule & Contract
  • Contract Duration: 3 months (Likely to extend)
  • Schedule: Monday-Friday, 8:00 AM-5:00 PM
  • Hours: 40 hours per week

Job Duties
We are seeking a Quality Control Analyst to support analytical testing activities within a cGMP-regulated biopharmaceutical manufacturing environment.
  • This role is responsible for executing and coordinating analytical testing of bulk drug substance and drug product across multiple analytical platforms, including chromatography, potency/bioassays, microbiology, raw materials, cleaning validation, and packaging testing.
  • The analyst will independently perform and review 3-5 analytical methods, ensure accurate documentation, and support data trending, investigations, and compliance activities.
  • Responsibilities include authoring and maintaining QC documentation (SOPs, test methods, specifications, and reports), identifying process improvements, and ensuring adherence to global regulatory requirements (e.g., FDA, EMA).

Qualifications
  • 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
  • Strong technical knowledge of analytical testing in biopharmaceutical manufacturing
  • Demonstrated ability to independently execute methods, review data, and ensure compliance.

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