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Full Time Fda Inspector Jobs in California (NOW HIRING)

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

Sanitation Supervisor

Corona, CA · On-site

$79K - $85K/yr

Corona, California Position Type: Full-time Classification: Exempt Shift: Flexible Salary Range ... inspections is preferred. * HACCP and SQF certifications are preferred. * FDA and/or USDA ...

... FDA, USDA, GMP, HACCP, and company food safety standards. * Conduct routine inspections of the ... AD&D Insurance Schedule Full-Time Schedule may vary based on operational needs. Compensation $70 ...

Showing results 21-40

Full Time Fda Inspector information

What is the difference between Full Time Fda Inspector vs Part Time Fda Inspector?

AspectFull Time Fda InspectorPart Time Fda Inspector
CredentialsTypically requires a bachelor's degree in life sciences or related field, plus FDA inspector certificationSame as full-time, but may have more flexible certification requirements
Work EnvironmentFull-time, on-site inspections at manufacturing facilities, laboratories, and warehousesPart-time, often involves scheduled inspections or follow-ups
Employer & Industry UsageFDA, government agencies, regulated industriesFDA, contractors, or consulting firms

Full Time Fda Inspectors work primarily on-site, conducting regular inspections and ensuring compliance with FDA regulations. Part Time Fda Inspectors perform inspections on a flexible schedule, often supplementing full-time staff. Both roles require similar credentials but differ mainly in hours and scope of work.

What are the key skills and qualifications needed to thrive as a full time FDA inspector?

To thrive as a Full Time FDA Inspector, you typically need a background in life sciences or a related field, strong analytical abilities, and knowledge of regulatory standards, often supported by a relevant bachelor's degree. Familiarity with inspection software, laboratory equipment, and FDA regulations, such as 21 CFR, is essential. Exceptional attention to detail, critical thinking, and effective communication skills help inspectors conduct thorough evaluations and collaborate with regulated entities. These skills ensure compliance with federal regulations, safeguarding public health and ensuring industry accountability.

What does a full time FDA inspector do?

A Full Time FDA Inspector is responsible for ensuring that products regulated by the Food and Drug Administration (FDA)—such as food, drugs, medical devices, and cosmetics—comply with all applicable laws and regulations. They conduct inspections of manufacturing facilities, review processes for safety and quality, collect samples for laboratory analysis, and document their findings. Their work helps protect public health by identifying and addressing potential risks before products reach consumers.

What are some common challenges faced by full time FDA inspectors during facility inspections?

Full Time FDA Inspectors often encounter challenges such as navigating complex manufacturing environments, ensuring compliance with evolving regulations, and effectively communicating findings to facility staff. Inspectors must balance thoroughness with efficiency, sometimes facing resistance or misunderstanding from inspected parties. Additionally, staying current on new product types and technologies can require ongoing training and adaptability, making collaboration with colleagues and subject matter experts essential.
What are the most commonly searched types of Fda Inspector jobs in California? The most popular types of Fda Inspector jobs in California are:
What cities in California are hiring for Full Time Fda Inspector jobs? Cities in California with the most Full Time Fda Inspector job openings:
Infographic showing various Full Time Fda Inspector job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 97% In-person, and 3% Remote job distribution.

Warehouse Receiving Coordinator

Life Science Outsourcing, Inc.

Brea, CA • On-site

$18.50 - $23.75/hr

Full-time

Posted 28 days ago


Job description

Company Description
(www.lso-inc.com) is in North Orange County in the city of Brea, California. Life Science Outsourcing, Inc (LSO) is a contract manufacturer of medical devices with in-built capabilities to offer clients full-service solutions through our six divisions. Clients rely on LSO to perform all activities required to introduce their products to market, from sourcing to drop shipping.
Be the first checkpoint for materials that become life-changing medical devices.
Life Science Outsourcing (LSO) is a trusted contract manufacturing partner to the medical device industry, providing manufacturing, assembly, packaging, and sterilization solutions in an FDA-registered, ISO 13485 certified environment. As our Warehouse Receiving Coordinator in Brea, California, you will be the front door of our supply chain, making sure every component that enters our facility is verified, documented, and traceable before it ever reaches production. The accuracy of your work directly protects product quality and patient safety.
You will thrive here if you take pride in precision, enjoy keeping a busy dock organized and moving, and understand that in a regulated environment, the paperwork matters just as much as the pallet. If you want your warehouse experience to count for something bigger, this role puts you at the center of it.
We encourage you to submit a resume with salary requirements.
Job Description
What You'll Do
As Warehouse Receiving Coordinator, you will own the dock-to-stock process for incoming materials:
Receiving and Verification
  • Receive and unload incoming shipments and verify quantities, part numbers, and lot numbers against purchase orders.
  • Check shipments for damage, correct labeling, and required documentation such as certificates of conformance.
  • Resolve receiving discrepancies quickly by working with Purchasing and suppliers.

Inventory and Material Flow
  • Process receipts in our ERP system and route materials to quarantine, incoming inspection, or stock.
  • Maintain accurate inventory records, lot traceability, and organized storage locations.
  • Support cycle counts and physical inventories, and help investigate discrepancies.

Quality and Compliance
  • Complete receiving records in real time following Good Documentation Practices.
  • Follow SOPs governing material handling in our FDA 21 CFR Part 820 and ISO 13485 certified facility.
  • Identify, segregate, and document nonconforming or damaged materials.

Teamwork and Coordination
  • Communicate receipt status and material availability to Purchasing, Planning, Quality, and Production.
  • Partner with Incoming Inspection to prioritize urgent materials for production.
  • Pitch in on shipping, kitting, and other warehouse functions during peak periods.

Safety
  • Operate pallet jacks and forklifts safely following training and certification.
  • Keep work areas clean, organized, and aligned with 5S and site safety standards.

Qualifications
What You Bring
Skills and Experience
  • 3+ years of experience in warehouse receiving, inventory control, or materials handling.
  • Hands-on experience processing receipts and transactions in an ERP or WMS system.
  • Strong attention to detail verifying part numbers, quantities, lots, and documentation.
  • Solid computer skills, including transaction entry, email, and basic Excel.
  • High school diploma or GED.

Mindset and Impact
  • You follow written procedures precisely and understand why documentation matters in a regulated industry.
  • You stay organized and keep priorities straight when the dock gets busy.
  • You communicate clearly across teams and flag problems early instead of letting them slide.
  • You take ownership of your area and hold a high standard for accuracy and housekeeping.

Compensation
The expected pay range for this position is [$XX.XX to $XX.XX per hour] depending on experience, qualifications, and internal equity. LSO reviews compensation regularly and offers competitive pay aligned with market benchmarks for the Brea, California area.
Why Join LSO?
  • Do work that matters: the materials you receive become finished medical devices that improve and save lives.
  • Build regulated-industry expertise in an FDA-registered, ISO 13485 certified facility, a credential that travels with your career.
  • Join a stable, growing company serving leading medical device innovators.
  • Work with a collaborative team where warehouse, quality, and production partner daily.
  • Grow your skills through cross-training in inspection, inventory control, and shipping.

Work Environment
  • Warehouse and receiving dock environment with material handling equipment traffic.
  • Regular lifting up to 50 pounds; standing, walking, bending, and reaching for most of the shift.
  • Safety shoes required in warehouse areas; additional PPE for specific tasks.
  • Occasional gowned entry into controlled or production areas.
  • Full-time, on-site, standard day shift with occasional overtime during peak periods and inventories.

Make an Impact
Every device we ship starts at your dock. When you verify a lot number, catch a discrepancy, or keep a receipt audit-ready, you are protecting the patients who depend on the products LSO helps bring to market. If you are ready to bring three or more years of warehouse expertise to a role where precision truly matters, we want to hear from you. Apply today and help us deliver quality from the very first touchpoint.
Additional Information
All your information will be kept confidential according to EEO guidelines.