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Contract Laboratory Jobs in Riverside, CA (NOW HIRING)

BioPhase Solutions

QA Specialist

Anaheim, CA

$25 - $35/hr

Proficient experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations. * Proficient experience and ...

Certified Group

Laboratory Manager

Tustin, CA

... laboratory testing, regulatory consulting, and certification & audit services across highly ... Labstat - A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp ...

Abbott

Contracts Manager, US

Lake Forest, CA

$94K - $126K/yr

... laboratory's most trusted and preferred source for molecular diagnostic solutions. We are a ... Act as a consultant and subject matter expert (SME) relative to customer contract language, terms ...

Abbott

Contracts Manager, US

Lake Forest, CA

$94K - $126K/yr

... laboratory's most trusted and preferred source for molecular diagnostic solutions. We are a ... Act as a consultant and subject matter expert (SME) relative to customer contract language, terms ...

Astrix Inc

QC Laboratory Technician

Anaheim, CA · On-site

$20.75 - $26.25/hr

M-F 8:00AM-4:30PM (OT when needed) Type : 6-month contract-to-hire Key Responsibilities * Conduct testing on raw materials, in-process samples, and finished goods following established laboratory ...

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All JobsContract Laboratory JobsContract Laboratory Jobs in Riverside, CA

Contract Laboratory information

See Riverside, CA salary details

$10

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$47

How much do contract laboratory jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for contract laboratory in Riverside, CA is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $20.05 and $29.09 per hour, depending on experience, location, and employer.

What is the difference between Contract Laboratory vs Quality Control Technician?

AspectContract LaboratoryQuality Control Technician
CredentialsRelevant scientific degrees, certifications in lab testingTechnical certifications, industry-specific training
Work EnvironmentIndependent labs, contract-based projectsManufacturing or production facilities
Employer & Industry UsageContract labs serve multiple clients across industriesManufacturers, quality departments in various industries

Contract laboratories focus on providing independent testing services for clients, often working on multiple projects across industries. Quality Control Technicians work within companies to monitor and ensure product quality during manufacturing. While both roles require technical skills and lab experience, contract labs emphasize external testing services, whereas QC Technicians focus on internal quality assurance.

What are the key skills and qualifications needed to thrive in a Contract Laboratory role, and why are they important?

To thrive in a Contract Laboratory role, a strong background in laboratory science, analytical techniques, and quality control principles—typically supported by a relevant science degree—is essential. Familiarity with laboratory information management systems (LIMS), regulatory standards (such as GLP or ISO/IEC 17025), and specialized analytical instruments is commonly required. Strong attention to detail, organization, and effective communication are crucial soft skills for managing projects and ensuring precise results. These competencies ensure accurate testing, regulatory compliance, and reliable service delivery for clients.

Who gets paid more, MLS or MLT?

In the context of a contract laboratory, Medical Laboratory Scientists (MLS) typically earn higher salaries than Medical Laboratory Technicians (MLT) due to advanced education and responsibilities. MLS professionals often hold a bachelor's degree and may have certification, leading to higher pay compared to MLTs, who usually have an associate degree and perform more routine tasks.

What are the 12 laboratory departments?

A contract laboratory typically includes departments such as chemistry, microbiology, environmental testing, toxicology, food safety, pharmaceuticals, clinical diagnostics, materials testing, quality assurance, research and development, instrumentation, and regulatory compliance. These departments work together to perform specialized tests and analyses based on client needs, often requiring knowledge of laboratory techniques and safety protocols.

What are some common challenges faced when working in a contract laboratory setting?

Professionals in contract laboratories often work on projects for multiple clients, which can lead to shifting priorities and tight deadlines. Balancing quality standards for various industries (such as pharmaceuticals, food, or environmental testing) requires strong attention to detail and adaptability. Effective communication and collaboration with both internal team members and external clients are essential to ensure requirements are met and results are delivered on time. Additionally, staying current with changing regulations and laboratory best practices is key to maintaining compliance and client trust.

What is the highest paying job in a laboratory?

In a laboratory setting, senior roles such as Laboratory Director or Principal Scientist tend to be the highest paying positions, often requiring advanced degrees and extensive experience. These roles involve overseeing operations, research, and compliance, and can earn six-figure salaries depending on the industry and location.

What is a contract laboratory?

A contract laboratory is a facility hired by companies or organizations to perform specific testing, analysis, or research services on samples or products. These labs operate under contractual agreements and often require specialized skills, equipment, and adherence to industry standards. They are commonly used in industries such as pharmaceuticals, environmental testing, and manufacturing.
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Contract Laboratory jobs near you
QA Specialist

QA Specialist

BioPhase Solutions

Anaheim, CA

$25 - $35/hr

Full-time

Posted 4 days ago

Job description

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company.

Pay Rate: $25-35/hour depending on experience.

Summary:
Review GMP technical documentation to ensure quality standards are met and compliant with applicable SOPs, US FDA 21CFR210, 211, 11 and applicable ICH guidance documents. Develop and revise QA procedures to strengthen cGMP compliance.

Responsibilities:
  • Performing timely review of batch records, test results and supporting technical documentation. Work closely with QA management to proactively address the quality of documentation.
  • Collaborating effectively with operations management to review and approve: SOPs, protocols, reports, equipment qualifications and calibrations, change controls, specifications, and other quality, documentation.
  • Providing assistance during cGMP compliance inspections of the facility by clients, the FDA and/or other regulatory bodies. This includes coordinating the retrieval of quality documents/records/trend data and any other documentation requested during these inspections.
  • Providing support for execution of the supplier assurance program at the site
  • Supporting review and release of raw materials and final product.
  • Providing cGMP compliance guidance and advice as needed.
  • Reviewing and approve deviations.
  • Supporting QA management in gathering data necessary for tracking quality metrics.
  • Maintaining workspace cleanliness by adhering to the 5S method of organization.
  • Abiding by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor.
  • This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.
Qualifications:
  • Preferred 2 – 3 years industry related work experience.
  • Bachelor's degree or equivalent in scientific discipline required.
  • Proficient experience and knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to contract laboratory and/or aseptic manufacturing operations.
  • Proficient experience and knowledge of USP, Pharm. Eur. (EudraLex) and other applicable standards.
  • Proficient knowledge of root cause investigation and problem solving; experience in the use of 5 Whys and/or other appropriate root cause investigation tools.
  • Proficient experience and knowledge in the use of LIMS and electronic documentation systems (i.e. MasterControl).
  • Works on problems of diverse scope; exercises good judgement in selecting methods and techniques for obtaining solutions while handling Quality Assurance tasks.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, etc.).

Please send resumes to mia@biophaseinc.com and visit our website at www.biophaseinc.com for additional job opportunities!!!