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Weekend Qc Stability Jobs (NOW HIRING)

QC Analyst I

Vacaville, CA Β· On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes ...

Stability Manager

San Carlos, CA Β· On-site

$147K - $171K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

The position may also require to conduct investigation for non-conforming materials, assist with shelf-life sample handling, and Online QC backup, sometimes off hour, weekend QC backup. ESSENTIAL ...

This is a weekend shift position; Friday, Saturday, Sunday 7AM-7PM The Quality Technician helps ... ESD Control, and familiarity handling ESD sensitive components * Ability to accurately read and ...

Stability Manager

San Carlos, CA Β· On-site

$134K - $162K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Data management to support the Stability Programs including the administration and distribution of Quality Control (QC) stability samples, associated document coordination, and collection and ...

This is a weekend shift position; Friday, Saturday, Sunday 7AM-7PM The Quality Technician helps ... ESD Control, and familiarity handling ESD sensitive components * Ability to accurately read and ...

This is a weekend shift position; Friday, Saturday, Sunday 7AM-7PM The Quality Technician helps ... ESD Control, and familiarity handling ESD sensitive components * Ability to accurately read and ...

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How much do weekend qc stability jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for weekend qc stability in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

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Infographic showing various Weekend Qc Stability job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 67% Full Time, 26% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

QC Analyst I

Vacaville, CA β€’ On-site

TekWissen LLC
Recruiting and Staffing ServicesΒ β€’Β 501 - 1,000 employees

$20 - $25/hr

Temporary

Re-posted 17 days ago


Job description

Overview:  
 
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological expertise with world-class manufacturing and scientific insight to support the delivery of innovative medicines for a wide range of diseases. Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, and cell and gene therapy, the company provides comprehensive services across the pharmaceutical, biotech, and life sciences sectors. It supports every stage of drug development, from early research to commercial production, and offers solutions in biologics, small molecules, and specialty ingredients. Committed to quality and innovation, the company serves as a critical partner in advancing therapeutic solutions and streamlining complex manufacturing processes, with a global presence that ensures access to scalable, flexible, and compliant technical expertise.
 
 
Job Title:         QC Analyst
Location:         Vacaville, CA
Duration:        6 months 
Job Type:        Temporary Position
Work Type:    Onsite
 
 
Summary
 
The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes execution of trend analysis, documentation review, deviation support (OOS, OOT, OOE), and general laboratory support activities. The coordinator works closely with Quality Control leadership to achieve departmental and organizational objectives.
 
Key Accountabilities:
  • Review analytical data against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and establish limits
  • Conduct routine and non-routine Out of Trend (OOT) linear regression assessments
  • Support deviations including OOS, OOT, and OOE investigations
  • Provide input into quality investigations and CAPA initiatives
  • Identify and troubleshoot technical issues
  • Identify gaps in systems and procedures
  • Develop Stability Protocols
  • Conduct stability deviation assessments
  • Create and review Routine Master Data Testing
  • Assist in Annual Product Quality Reviews (APQRs) authoring
  • Support time point approval activities
  • Manage change control documentation
  • Handle data table requests and annual report requests (including client monitor requests)
  • Participate in stability-related projects and process improvement initiatives
  • Perform data entry and review
  • Support training coordination
  • Maintain GMP compliance in all operational areas
  • Coordinate with customers for multi-site operational support
  • Support internal audits, external audits, and regulatory inspections
  • Work effectively to meet schedules, timelines, and deadlines
  • Participate in and/or lead cross-functional project teams
  • Perform additional quality-related duties as assigned
Required Qualifications
  • B.S./B.A. degree in a relevant scientific discipline
  • 1–3 years of experience in the pharmaceutical or biopharmaceutical industry (or equivalent combination of education and experience)
  • Knowledge of cGMP regulations and quality systems
  • Experience in stability program management
  • Exposure to regulatory inspections and audit support
  • Experience with CAPA, deviation investigations, and change control processes
  • Knowledge of trend analysis and statistical data evaluation
  • Experience supporting multi-site operations
  • Familiarity with APQR documentation and authoring support
  • Strong verbal and written communication skills
  • Ability to organize and present information formally and informally
  • Working knowledge of scientific theories, principles, and analytical/biological testing techniques
  • Strong problem-solving, reasoning, and analytical skills
  • Ability to exercise sound judgment
  • Capable of working independently with limited supervision
  • Ability to prioritize short-term tasks effectively
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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