Find Jobs
Find Jobs Near You – Available Work in Your Location
QC Inspector Incoming Inspection
Career Insights for Quality Control Analyst
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on California data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$67,470 / year median in California
-12% projected decline
Job Description
Full Job Description Position Summary:
We are seeking a knowledgeable and hands-on QC Inspector for inspection of incoming finished products, components and packaging materials. The ideal candidate brings strong experience in incoming QC and documentation control within the manufacturing of cosmetics, OTC drugs, dietary supplements, and potentially medical devices.Key Responsibilities:
To prepare, update and maintain finished good (FG), component & packaging materials master's for outside manufactured or assembled products. To perform control of FG, component & packaging materials from receipt to release as per SOP. To perform form/fit/function and dimensional analysis where required for finished goods (FG), components and packaging materials. To sample, inspect and release FGs, component & packaging materials on time. To prepare and maintain the inspection reports. To keep inspection release log up to date. To monitor reworked or rejected FGs, components and packaging materials to ensure products are being reworked or disposed properly. To identify and control nonconforming FGs, components & packaging materials and assist in determining root cause, corrective/preventive actions. To review the GMP compliance in warehouse area to ensure FGs, Components and packaging materials are not contaminated during handling and storage. To review the Pest control process of the warehouse. Report any unusual quality incident to immediate supervisor in a timely manner. Other duties and responsibilities as required by Management.Qualifications:
Minimum 2-3 years of progressive experience in Quality Control and/or Assurance within OTC Drug and Dietary Supplement manufacturing Experience with cGMP, incoming QC inspection, AQL sampling plan and knowledge of using the measuring tools like vernier caliper, micrometer etc. Ability to lead by example and drive quality culture in the warehouse Speak and write English Basic mathematics skills Basic computer skills Responsibilities may be shifted based on the department and company's demand Flexibility in work schedulePay:
$25.00 - $30.00 per hourBenefits:
401(k) Dental insurance Health insurance Life insurance Paid time off Vision insurance Application Question(s): How many years of hands-on QC inspection experience do you have specifically with OTC drugs, dietary supplements, cosmetics, or medical devices? Can you walk me through your experience inspecting incoming finished goods, components, and packaging materials from receipt through release? What experience do you have using AQL sampling plans for incoming inspections, including determining whether materials should be accepted or rejected? Which measuring tools have you personally used, such as vernier calipers or micrometers, and what types of dimensional or form/fit/function inspections have you performed?Work Location:
In personBenefits
- Paid Time Off (PTO)
- 401(k) Plans
- Health Insurance
- Dental Insurance