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Quality Control Cmm Inspector Jobs in Oxnard, CA

Randstad

QC Lab Support Specialist

Thousand Oaks, CA

$35 - $40/hr

The QC Lab Support Analyst supports quality, compliance, and operational processes that enable ... The Analyst collaborates with internal stakeholders to maintain inspection-ready laboratory ...

Haas Automation Inc.

QC Eng 2 (51259)

Oxnard, CA · On-site

$30 - $40/hr

Create the inspection control for most process methods employed at Haas to ensure control of design ... quality, etc. • Employees must exhibit honesty and integrity as well as demonstrate adherence to ...

Haas Automation, Inc.

QC Eng 2 (51259)

Oxnard, CA · On-site

$30 - $40/hr

Create the inspection control for most process methods employed at Haas to ensure control of design ... quality, etc. • Employees must exhibit honesty and integrity as well as demonstrate adherence to ...

Eaton

Quality Technician III - 1st Shift

Camarillo, CA · On-site

$26 - $39/hr

What you'll do: • Maintain, troubleshoot, and validate CMM equipment for the Receiving Inspection ... or certification in Quality Control, Engineering Technology or related field. Additional ...

Haas Automation Inc.

QC Eng 2 (50866)

Oxnard, CA · On-site

$30 - $40/hr

Create the inspection control for most process methods employed at Haas to ensure control of design ... quality, etc. • Employees must exhibit honesty and integrity as well as demonstrate adherence to ...

NextDeavor Inc.

Quality Inspector 2

Simi Valley, CA

$20.80 - $26/hr

Conduct examinations and quality control inspections on products, materials, and components at multiple production stages * Perform routine visual and mechanical inspections of electronic and electro ...

Haas Automation, Inc.

QC Eng 2 (50866)

Oxnard, CA · On-site

$30 - $40/hr

Create the inspection control for most process methods employed at Haas to ensure control of design ... quality, etc. • Employees must exhibit honesty and integrity as well as demonstrate adherence to ...

NextDeavor Inc.

Quality Inspector 2

Simi Valley, CA · On-site

$20.80 - $26/hr

Conduct examinations and quality control inspections on products, materials, and components at various production stages to verify compliance with specifications * Perform visual and mechanical ...

Crossroads Staffing Services, Inc.

Be Seen First

IPC Quality Inspector

Oxnard, CA · On-site

$25 - $30/hr

The Quality Inspector will be responsible for performing first article, incoming and final inspections for all level boards and components as well as record results of completed assemblies in ...

Belcan

Quality Inspector 2

Simi Valley, CA

$25 - $26/hr

Responsibilities: · Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established ...

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Quality Control Cmm Inspector information

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How much do quality control cmm inspector jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for quality control cmm inspector in Oxnard, CA is $22.74, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $25.43 per hour, depending on experience, location, and employer.

What is a quality control CMM inspector?

Quality Control CMM Inspectors are professionals who use Coordinate Measuring Machines (CMM) to ensure that manufactured parts and products meet precise specifications and quality standards. They set up and operate CMM equipment to measure the dimensions and features of components, comparing them to engineering drawings and tolerances. These inspectors play a crucial role in quality assurance by identifying defects, maintaining detailed inspection records, and supporting continuous improvement in manufacturing processes.

How does a quality control CMM inspector typically collaborate with other departments during the inspection process?

A Quality Control CMM Inspector frequently works closely with manufacturing, engineering, and quality assurance teams to ensure that components meet precise specifications. Inspectors often communicate their findings, such as dimensional discrepancies or process issues, to engineers and production supervisors, enabling quick resolution and continuous improvement. This collaborative approach helps maintain product quality, streamline workflows, and prevent costly errors. Regular meetings and clear documentation are common practices to ensure everyone stays informed and aligned.

What are the key skills and qualifications needed to thrive as a quality control CMM inspector, and why are they important?

To thrive as a Quality Control CMM Inspector, you need a solid understanding of precision measurement, blueprint reading, and quality assurance principles, often supported by relevant technical training or certifications. Proficiency with Coordinate Measuring Machines (CMM), software such as PC-DMIS or Calypso, and familiarity with GD&T (Geometric Dimensioning and Tolerancing) standards are typical requirements. Attention to detail, analytical thinking, and strong communication skills help inspectors identify defects and interact effectively with production teams. These skills ensure accurate inspections, compliance with specifications, and the delivery of high-quality products.

What is the difference between Quality Control Cmm Inspector vs Quality Control Inspector?

AspectQuality Control Cmm InspectorQuality Control Inspector
CertificationsOften requires CMM programming and inspection certificationsTypically requires general quality inspection certifications
Work EnvironmentPrimarily in manufacturing or machining facilities, using CMM machinesIn various industries, inspecting products, parts, or assemblies
ResponsibilitiesMeasuring parts with Coordinate Measuring Machines (CMM), ensuring dimensional accuracyPerforming visual and dimensional inspections, documenting quality issues

The main difference is that a Quality Control Cmm Inspector specializes in using CMM equipment to perform precise measurements, while a Quality Control Inspector may perform a broader range of inspection tasks. Both roles are essential in manufacturing, but the CMM Inspector focuses more on advanced measurement techniques and equipment.

What are popular job titles related to Quality Control Cmm Inspector jobs in Oxnard, CA?

For Quality Control Cmm Inspector jobs in Oxnard, CA, the most frequently searched job titles are:

What job categories do people searching Quality Control Cmm Inspector jobs in Oxnard, CA look for?

The top searched job categories for Quality Control Cmm Inspector jobs in Oxnard, CA are:

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Cities near Oxnard, CA with the most Quality Control Cmm Inspector job openings:

Quality Control Cmm Inspector jobs near you

Associate Director, Quality Assurance (GMP QC Lab Oversight)

Coherus Oncology

Camarillo, CA • On-site

Full-time

Re-posted 15 days ago

Job description

Title: Associate Director, Quality Assurance (GMP QC Lab Oversight)
Reports to: Head of Quality Assurance Operations
Location: Camarillo, CA (On-site)
Classification: Exempt
Overview:
The Associate Director, Quality Assurance provides strategic and operational QA oversight of GMP Quality Control laboratory activities at the Camarillo site and reports to the Head of QA Operations. This role requires a regular on-site presence to effectively support daily GMP QC laboratory operations.
Key responsibilities include ensuring compliant laboratory operations through oversight of laboratory systems, facilities, and the qualification and validation of instruments and equipment. The role is accountable for review and approval of Certificates of Analysis (CoAs) and other GMP documentation, supporting laboratory investigations and batch disposition decisions, and contributing to Quality Management Review processes. The Associate Director also serves as a key partner to QC in driving inspection readiness, continuous improvement, and sustained GMP compliance.
Responsibilities:
  • Provide QA oversight of GMP QC laboratory operations to ensure compliance with cGMP, FDA, and ICH requirements.
  • Oversee QC laboratory systems, instruments, and equipment throughout their lifecycle, ensuring they remain in a validated and inspection-ready state.
  • Review and approve QC-related GMP documentation, including analytical records, CoAs/CoTs, method qualification and validation reports, stability data, deviations, CAPAs, and change controls.
  • Lead and oversee laboratory investigations (e.g., OOS, OOT, deviations, and data integrity events), ensuring robust root cause analysis, appropriate impact assessment, and timely, compliant resolution.
  • Support batch disposition by ensuring QC data, CoAs, investigations, and associated documentation are complete, accurate, and compliant with internal procedures and regulatory expectations.
  • Partner cross-functionally with QC, Manufacturing, Regulatory, and site leadership to ensure compliant laboratory operations, drive continuous improvement, and maintain sustained inspection readiness.
  • Provide QA support and oversight for method transfer, validation, and technical transfer activities impacting QC laboratory operations.
  • Collaborate with Facilities, IT, and QC to support equipment implementation, qualification, maintenance, and resolution of operational issues impacting GMP laboratory activities.
  • Support and participate in internal audits, external audits, and regulatory inspections; contribute to inspection readiness activities and timely, effective responses.
  • Contribute to Quality Management Review processes (e.g., QMR, PQR/APQR), including analysis of QC performance metrics, identification of quality trends, and execution of continuous improvement actions.
  • Escalate significant quality risks and critical issues to the Head of Quality Assurance and senior leadership, as appropriate.
  • Drive development, enhancement, and continuous improvement of SOPs, QA processes, and QC-related quality systems.

Qualifications:
  • Bachelor's degree in a scientific discipline (or equivalent experience) with a minimum of 8 years of direct experience supporting GMP QC laboratory operations in a regulated pharmaceutical or biotechnology environment, including QA oversight.
  • Demonstrated experience in biologics/protein therapeutics, including manufacturing and testing of drug substance, drug product, and finished goods.
  • Demonstrated experience handling QC-related issues, records, and laboratory operations, including analytical documentation, deviations, and investigations, within a GMP environment; prior hands-on QC laboratory experience strongly preferred.
  • Experience reviewing and approving equipment and instrument qualification and validation documentation (e.g., IQ/OQ/PQ), with working knowledge of lifecycle management principles; experience applying risk-based approaches to computerized systems (GAMP 5) preferred.
  • Strong working knowledge of FDA cGMP regulations and ICH guidelines applicable to QC laboratory operations.
  • Experience leading and/or overseeing laboratory investigations, including OOS, OOT, deviations, CAPAs, change control, and data integrity events within a GMP environment.
  • Solid understanding of CoA/CoT generation and approval, and experience supporting batch disposition decisions in a GMP setting.
  • Demonstrated experience supporting internal audits, external audits, and regulatory inspections, including inspection readiness and response activities.
  • Strong written, verbal, and interpersonal communication skills, with the ability to effectively influence cross-functional teams.
  • Proven ability to exercise sound judgment, prioritize effectively, and operate successfully in a fast-paced, on-site GMP environment.

Additional requirements
  • On-site presence in Camarillo is required to support daily GMP QC laboratory operations.
  • Up to 20% travel may be required to support audits, external laboratories, or business needs.

The Base Salary Range for this position is $170,000 to $200,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.
Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.

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