Quality Control Technician Lead

Actalent; Camarillo (CA); On-site; USD 34,000 - 49,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

PTO/Sick leave

Job summary

Actalent is seeking a Quality Control Technician Lead for a contract-to-hire role in Camarillo, CA. The position oversees cleanroom inspections, calibration, and testing activities, ensuring regulatory compliance and precise documentation.

You will lead a team, supervise at least five staff, and uphold GMP and quality standards while collaborating with cross-functional teams and external partners.

Qualifications

• Bachelor's degree in a technical or scientific field or an equivalent combination of education and experience.
• Experience in regulated environments such as pharma/medical devices is required.
• Strong GMP, ISO, and CFR knowledge with established documentation practices.

Responsibilities

• Lead QC activities in a cleanroom, ensuring inspections are done accurately and on time.
• Manage calibration and maintenance of measuring devices and inventory.
• Support testing across manufacturing, including first article, in-process, and final inspections.
• Review documentation for completeness, accuracy, and regulatory compliance.

Skills

Quality leadership

GMP knowledge

GD&T

Calipers & micrometers

Blueprint reading

OOS investigations

Root cause analysis (RCA)

ISO 9001/13485

21 CFR parts 210/211/820

Environmental monitoring

Document control

Team supervision

Interdepartmental collaboration

Education

Bachelor's degree or HS diploma with 13 years QA experience

Tools

Calipers

Micrometers

Quality systems software

Job description

Job Title: Quality Control Technician LeadJob Description

The Quality Control Technician Lead works in a cleanroom environment and oversees the inspection of all incoming materials and final products. This role manages equipment calibration and maintenance, supports testing activities throughout manufacturing, and ensures that all quality control procedures are completed accurately and documented thoroughly. The position requires strong leadership skills, attention to detail, and the ability to work effectively in a fast-paced, regulated environment.

Responsibilities

• Lead quality control activities within the cleanroom, ensuring all receiving inspections and final product inspections are completed accurately and on time.




• Manage the equipment calibration and maintenance program, including maintaining an up-to-date inventory and status of all measuring devices such as calipers, micrometers, and precision measurement tools.




• Provide support for all aspects of testing related to manufacturing, including first article inspections, in-process release inspections, and final quality control release of finished goods.




• Conduct thorough document reviews to verify completeness, accuracy, and compliance with applicable procedures and regulations.




• Ensure that all inspections, tests, and procedures are properly performed, recorded, and controlled in accordance with internal quality systems and regulatory requirements.




• Support environmental monitoring of cleanrooms and the review of bioburden results, and contribute to identifying and implementing solutions for microbial failures.




• Review quality assessment results and make informed decisions on accepting or rejecting manufactured products during the inspection process, including handling out-of-specification (OOS) and non-conformance findings.




• Participate in investigations related to source materials, products, and components, including root cause analysis (RCA) for deviations and non-conforming materials.




• Complete customer surveys and questionnaires related to quality systems, product performance, and compliance as required.




• Interpret blueprints and technical drawings to perform accurate inspections and ensure products meet geometric dimensioning and tolerancing (GD&T) requirements.




• Lead and supervise a team, providing direction to at least five individuals, and ensure consistent adherence to Good Manufacturing Practices (GMP) and quality standards.




• Support and maintain document control processes, ensuring proper handling, storage, and retrieval of quality and inspection records.




• Collaborate with cross-functional teams, external vendors, and contractors to resolve quality issues and drive continuous improvement in quality processes.




• Promote a culture of quality, accountability, and continuous improvement within the team and the broader organization.

Essential Skills

• Bachelor's degree in a technical or scientific discipline, or a High School Diploma with 13 years of experience in quality assurance.




• Experience working in a pharmaceutical, medical device, or similarly regulated environment.




• Understanding of global pharmaceutical product regulations, including experience with ISO 9001 and/or ISO 13485:2003, and 21 CFR Parts 210 and 211 and/or Part 820.




• Hands-on experience with quality systems, including corrective actions, change control, quality audits, and validation of manufacturing processes or product development.




• Proven experience leading or supervising a team, including direct oversight of at least five individuals.




• Strong knowledge of Good Manufacturing Practices (GMP) and their application in a production or cleanroom environment.




• Demonstrated ability to perform quality inspections using tools such as calipers, micrometers, and other precision measurement instruments.




• Ability to read and interpret blueprints and technical drawings, including familiarity with geometric dimensioning and tolerancing (GD&T).




• Experience with first article inspections, in-process inspections, final inspections, and release of finished goods.




• Proficiency in handling non-conformance, deviation, and out-of-specification (OOS) investigations, including root cause analysis (RCA).




• Strong attention to detail and accuracy in inspection, documentation, and data review.




• Good general mathematical skills to support measurements, calculations, and data analysis.




• General computer skills, including the ability to enter, manage, and review data in electronic systems.




• Effective verbal and written communication skills and the ability to work collaboratively with internal teams and external partners.




• Ability to work efficiently and effectively in a team environment, supporting shared goals and timelines.




• Demonstrated integrity, sound judgment, strong work ethic, and personal accountability for results.




• Passion for innovation and drive to identify and implement practical solutions to quality challenges.




• Commitment to continuous learning, improvement, and an uncompromising dedication to quality.

Additional Skills & Qualifications

• Experience with environmental monitoring programs and interpreting bioburden or microbial test results.




• Familiarity with document control processes and systems in a regulated environment.




• Experience completing customer quality surveys and questionnaires.




• Strong organizational and planning skills, with the ability to prioritize tasks in a fast-paced setting.




• Good interpersonal skills for collaborating interdepartmentally and with external vendors and contractors.




• Experience with assembly processes and precision measurement in a production environment.




• Comfort working with labeling, documentation, and inspection records to ensure traceability and compliance.




• Demonstrated ability to handle multiple responsibilities while maintaining high standards of quality and accuracy.

Work Environment

This role operates primarily in a cleanroom environment and requires the ability to work in a high-paced setting while maintaining strict quality and cleanliness standards. The position involves frequent use of precision measurement tools such as calipers and micrometers, as well as regular use of computers for documentation, data entry, and review of inspection records. Work is performed under Good Manufacturing Practices (GMP) and within a structured quality system, including environmental monitoring and controlled documentation processes. The role involves close collaboration with production, quality, and other cross-functional teams, with a strong emphasis on teamwork, communication, and continuous improvement.

Job Type & Location

This is a Contract to Hire position based out of Camarillo, CA.

Pay and Benefits

The pay range for this position is $30.00 - $30.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)

Job Type & Location

This is a Contract to Hire position based out of Camarillo, CA.

Application Deadline

This position is anticipated to close on Nov 13, 2026.

Workplace Type

This is a fully onsite position in Camarillo,CA.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.