5 Quality Control jobs in Perris

Director, Quality Control Lab
Category: Quality
Position Type: Regular Full-Time
External ID: 18015
Location: Lake Forest, CA, United States
Date Posted: Oct 15, 2025
Hiring Range: 172,000.00 to 195,300.00 USD Annually
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**Overview**
POSITION SUMMARY STATEMENT:
The Director, Quality Control Lab will be responsible for managing all laboratory functions in Quality Control and will work with and train chemists and technicians to operate laboratory equipment, implement test procedures and ensure compliance in the Herbalife laboratories.
DETAILED RESPONSIBILITIES/DUTIES:
+ Provides leadership, guidance and direction to QC lab to support the department's and company's strategic initiatives and goals.
+ Work with our industry partners and scientific affiliates and contribute to the advancement of analytical technologies and method research.
+ Implement innovation ideas and continuous improvement activities
+ Initiate investigations for non-conforming product and develop Corrective and Preventive program.
+ Liaise with the regulatory authorities on laboratory operations.
+ Responsible for applying inspection standards to products shipped directly from contract manufacturers to outside locations.
+ Develop and maintain a system that assures all certificates of analyses are reviewed against required finished product specifications as written in Agile PLM (Product Lifecycle Management).
+ Periodically perform a mock recall to assure that the systems have qualified and acceptable traceability standards.
+ Develop training program for scientists and lab technicians to ensure compliance with Good Laboratory Practices and current Good Manufacturing Practices.
+ Support regulatory audit preparation.
+ Perform additional duties as assigned.
+ Develop metrics and reports to assess performance, trend and analyze data and take appropriate actions as appropriate. Track, report and provide periodic reports to management in support of Quality Metrics. Leverage data to improve product quality and laboratory efficiency.
+ Lead laboratory operations and maintain the laboratories in compliance with ISO17025 accreditation requirements and other applicable local laws/regulations.
SUPERVISORY RESPONSIBILITIES:
Manages chemists, technicians, and laboratory supervisors.
**Qualifications**
REQUIRED QUALIFICATIONS:
Skills:
+ Strong leadership skills with expertise in implementing quality processes, systems and strategies
+ Proven understanding in laboratories operations
+ Expertise in ISO17025 requirements
+ Strong proven hands-on experience with variety of both GMP and GLP matters
+ Strong verbal and written communication skills with ability to work with a high degree of accuracy and detail
+ Strong interpersonal skills and the ability to work well as part of a team
Experience:
+ 10+ years of laboratory operations experience
Education:
+ Bachelor's degree in life sciences or equivalent technical field.
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At Herbalife, we value doing what's right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected characteristic. We value diversity, strive for inclusivity, and believe the differences among our teammates is a key contributor to Herbalife's ongoing success.
Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability and an Employee Assistance Program (EAP).
Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.
If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please email your request to

.
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Job Title: Quality Assurance Technician
Job Description
We are seeking a meticulous Quality Assurance Technician to organize and maintain GMP, ISO, and manufacturing documents. The role involves routine desk work, filing and retrieving documents, assisting with internal audits and QA investigations, and supporting training programs for manufacturing staff.
Responsibilities
+ Organize and maintain GMP, ISO, and manufacturing documents.
+ Perform routine desk work such as filing and retrieving documents.
+ Assist with internal audits and QA investigations.
+ Support training programs for manufacturing staff.
+ Collect and analyze manufacturing data to identify risks.
+ Maintain tracking systems for customer complaints.
+ Review documents for accuracy and compliance.
+ Release raw materials and inspect production lines.
Essential Skills
+ 1-2 years of QA experience, preferably in the nutraceutical or pharmaceutical industry.
+ Strong experience in documentation within a related industry.
+ Familiarity with GMPs is highly desirable.
+ Proficiency in Microsoft Office (Word/Excel).
+ Skills in managing and organizing documents.
Additional Skills & Qualifications
+ Experience in the nutraceutical manufacturing field is beneficial.
+ Data entry skills.
Work Environment
The position is based in a nutraceutical manufacturing company and requires full-time on-site work from Monday to Friday, 7 am to 3:30 pm. The role involves working in an office setting, with some interactions with a Document Clerk and two QA Inspectors. The candidate will report to the QA/QC team.
Job Type & Location
This is a Contract to Hire position based out of Jurupa Valley, California.
Pay and Benefits
The pay range for this position is $21.00 - $23.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Jurupa Valley,CA.
Application Deadline
This position is anticipated to close on Oct 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Quality Assurance Technician
Job Description
We are seeking a meticulous Quality Assurance Technician to organize and maintain GMP, ISO, and manufacturing documents. The role involves routine desk work, filing and retrieving documents, assisting with internal audits and QA investigations, and supporting training programs for manufacturing staff.
Responsibilities
+ Organize and maintain GMP, ISO, and manufacturing documents.
+ Perform routine desk work such as filing and retrieving documents.
+ Assist with internal audits and QA investigations.
+ Support training programs for manufacturing staff.
+ Collect and analyze manufacturing data to identify risks.
+ Maintain tracking systems for customer complaints.
+ Review documents for accuracy and compliance.
+ Release raw materials and inspect production lines.
Essential Skills
+ 1-2 years of QA experience, preferably in the nutraceutical or pharmaceutical industry.
+ Strong experience in documentation within a related industry.
+ Familiarity with GMPs is highly desirable.
+ Proficiency in Microsoft Office (Word/Excel).
+ Skills in managing and organizing documents.
Additional Skills & Qualifications
+ Experience in the nutraceutical manufacturing field is beneficial.
+ Data entry skills.
Work Environment
The position is based in a nutraceutical manufacturing company and requires full-time on-site work from Monday to Friday, 7 am to 3:30 pm. The role involves working in an office setting, with some interactions with a Document Clerk and two QA Inspectors. The candidate will report to the QA/QC team.
Job Type & Location
This is a Contract to Hire position based out of Jurupa Valley, California.
Pay and Benefits
The pay range for this position is $21.00 - $23.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Jurupa Valley,CA.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Quality Assurance Inspector - 2nd Shift
Category: Quality
Position Type: Regular Full-Time
External ID: 17675
Location: Lake Forest, CA, United States
Date Posted: Oct 20, 2025
Hiring Range: 19.00 to 21.85 USD Hourly
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**Overview**
THE ROLE:
The Quality Assurance Technician (I) will be responsible for the sampling of components, physical testing of in-process materials and finished goods, reserve sample arrangements, related documentation and other tasks as assigned by management, while working in a team environment.
HOW YOU WOULD CONTRIBUTE:
+ Support manufacturing and production operations.
+ Perform line inspections by adhering to GMPs and SOPs
+ Collect samples for submission to state regulatory agency.
+ Sample and perform inspections of components
+ Determine disposition of components and release or reject as appropriate
+ Performance of organoleptic and physical analyses to include brix, pH, LOD, and specific gravity determination.
+ Review of documentation - test results for components and QA inspection documentation to assure material meets specifications
+ Ensure adherence with GMPs and SOPs; responsibilities include, performing sampling, inspection and documentation review activities as required
+ Assisting in determination of corrective action as required
+ Assist management in conducting formal procedural inquiries and investigations to determine the cause of quality problems, recommend verbal and/or written corrective action to management as required
+ Interact effectively with co-workers, management, and vendors to resolve problems
+ Assist management with development of departmental goals and objectives
+ Other duties as assigned
WHAT'S SPECIAL ABOUT THE TEAM:
Strong collaborative work environment dedicated to enhancing the team's skill sets.
**Qualifications**
SUPERVISORY RESPONSIBILITIES:
Not applicable for this position
SKILLS AND BACKGROUND REQUIRED TO BE SUCCESSFUL:
Skills:
+ Strong interpersonal and communication skills
+ Ability to communicate effectively both verbally and in written English
+ Computer literacy, with solid PC and software experience
+ Ability to lift a minimum of 30lbs
+ Strong ability to work independently and as a team member under the pressure of manufacturing
Experience:
+ Previous knowledge and understanding of Quality compliance
+ A minimum of one year experience in QA/QC.
+ Working knowledge of cGMP and regulatory guidelines
+ Ability to problem solve efficiently under the pressure of a production environment
+ Knowledge of basic cGMP and QA/QC regulations for the food, pharmaceutical or medical device industry.
+ Familiarity with safe work practices to include proper Personal Protective Equipment (PPE), allergen control, and proper sample handling and disposal
Education:
+ High School diploma or GED equivalent
PREFERRED QUALIFICATIONS:
+ Previous experience working in a food or dietary supplement manufacturing plant Quality Assurance setting
+ Bachelor's degree in Technical or Science related discipline
+ Better Process Control School Certification
+ HACCP Certification
+ ASQ, Six Sigma, or applicable certifications
+ Experience with Oracle, Agile, Master Control
+ High degree of attention to detail
+ Proficiency in Microsoft Office products - MS Windows, Word, and Excel
At Herbalife, we value doing what's right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected characteristic. We value diversity, strive for inclusivity, and believe the differences among our teammates is a key contributor to Herbalife's ongoing success.
Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability and an Employee Assistance Program (EAP).
Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.
If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please email your request to

.
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