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Quality Control In Jobs in Calabasas, CA (NOW HIRING)

Teledyne FLIR LLC

Quality Control Manager

El Segundo, CA · On-site

$120K - $160K/yr

Oversee Receiving, In-Process, Final, and Shipping inspections, including AS9102 First Article ... Maintain QC KPIs, inspection instructions, and continuous improvement initiatives. * Support ...

NEP Group

Quality Control Technician

Van Nuys, CA · On-site

$18 - $20/hr

The QC technician is responsible for testing equipment in the NEP Rentals Inventory to ensure it is operating properly. The QC technician will also configure equipment to the client specifications ...

Astrix Inc

QC Chemist

Los Angeles, CA · On-site

... a skilled QC Chemist to join their team in Los Angeles County, CA! Job type: Contract- hire ... Pull and test raw materials, in-process samples, and finished goods to ensure compliance with ...

Marvin Group

SUPERVISOR QUALITY CONTROL

Inglewood, CA · On-site

$28.85 - $36.35/hr

Based in Southern California near the Los Angeles International Airport, The Marvin Group consists ... Quality Control Supervisor provides support to the QC manager by overseeing and working alongside ...

The Right Hire

Quality Control Specialist

Vernon, CA · On-site

$20 - $23/hr

The ideal candidate will have experience in quality control, manufacturing, metal finishing, anodizing, aluminum products, or window and door production. This role requires strong attention to detail ...

Kelly Services

QC Manager

San Fernando, CA

$90K - $120K/yr

QC Manager Kelly ® Science & Clinical is seeking a QC Manager for a contract-to-hire position at a ... In this role, you will oversee the testing of raw materials, in-process and finished products, and ...

Marvin Group

SUPERVISOR QUALITY CONTROL

Inglewood, CA · On-site

$28.85 - $36.35/hr

Based in Southern California near the Los Angeles International Airport, The Marvin Group consists ... Quality Control Supervisor provides support to the QC manager by overseeing and working alongside ...

Arixa Capital

QC Analyst

Los Angeles, CA · On-site

$25.75 - $34.75/hr

Our vertically integrated platform allows us to manage every step of the loan process in-house ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

Arixa Capital

QC Analyst

Los Angeles, CA · Hybrid

$25.75 - $34.75/hr

Our vertically integrated platform allows us to manage every step of the loan process in-house ... The QC Analyst will analyze data for consistency, identify discrepancies, correct mistakes, and ...

BioPhase Solutions

QC Microbiologist

Los Angeles, CA

$20 - $24/hr

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiologist to work for a Greater Los ...

Actalent

Quality Control Chemist

South Gate, CA

$22 - $26/hr

Quality Control Chemist Chemical company in South Gate is looking for a QC Chemist to join their team! The Quality Control Chemist is responsible for testing and inspecting products at various stages ...

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Showing results 21-40

All JobsQuality Control In JobsQuality Control In Jobs in Calabasas, CA

Quality Control In information

See Calabasas, CA salary details

$32.3K

$86.1K

$137.2K

How much do quality control in jobs pay per year?

As of Aug 16, 2026, the average yearly pay for quality control in in Calabasas, CA is $86,147.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,100.00 and $105,900.00 per year, depending on experience, location, and employer.

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

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What cities near Calabasas, CA are hiring for Quality Control In jobs?

Cities near Calabasas, CA with the most Quality Control In job openings:

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Calabasas, CA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $86,147 per year, or $41.4 per hour.

Associate Director, Quality Assurance (GMP QC Lab Oversight)

Coherus Oncology

Camarillo, CA • On-site

Full-time

Re-posted 12 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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