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Assistant Biotech Quality Control Jobs in California

The QC Inspector examines items for defects in materials, work, and damage. The Inspector is ... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ...

The QC Inspector examines items for defects in materials, work, and damage. The Inspector is ... pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is ...

Investigation and Data Review: Assist in data trending and data review for conformance to ... biotech QC labs, including hands-on raw material testing under cGMP. Knowledge, Skills, and ...

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Responsibilities: * Assist in managing projects and technical activities associated with method ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Perform trend analysis and assist in establishing limits * Identify discrepancies and support ...

Quality Control Lab Assistant

Santa Ana, CA · On-site

$20.84 - $27.19/hr

The Quality Control Lab Assistant will support the QC Department under the direction of a QC Lead ... biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Perform trend analysis and assist in establishing limits * Identify discrepancies and support ...

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Assistant Biotech Quality Control information

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

What are the most commonly searched types of Biotech Quality Control jobs in California? The most popular types of Biotech Quality Control jobs in California are:
What job categories do people searching Assistant Biotech Quality Control jobs in California look for? The top searched job categories for Assistant Biotech Quality Control jobs in California are:
What cities in California are hiring for Assistant Biotech Quality Control jobs? Cities in California with the most Assistant Biotech Quality Control job openings:

Quality Control Inspector

KORE1 Technologies

Irvine, CA • On-site

$26 - $28/hr

Contractor

Re-posted 16 hours ago


Job description

KORE1, a nationwide provider of staffing and recruiting solutions, has an immediate opening for a Quality Control Inspector in Irvine, Ca
About the Role:
The Quality Control (QC) Inspector inspects purchased parts, assemblies, accessories, and materials for conformance to requirements and specifications. The QC Inspector examines items for defects in materials, work, and damage. The Inspector is responsible for ensuring conformance of incoming materials to the requirements of medical device components and finished goods.
Essential Duties and Responsibilities:
* Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
* Records inspection and test data as prescribed by written instructions and procedures.
* Reviews supplier-provided documentation to determine compliance with specifications and drawings; maintains accurate and complete records for each part, including the Receiving Inspection (RI) log; completes, scans, and files RI quality records; and ensures status is updated electronically in the Enterprise Resource Planning system.
* Label all inspected components and materials accordingly, following visual inspection and final disposition.
* Work collaboratively and communicate proactively with Procurement, R&D Engineering, Manufacturing Engineering, Receiving, and other departments to ensure timely and high-quality execution of RI responsibilities.
* Strictly comply with standard operating procedures and work instructions, recommending improvements and enhancements to processes, and performing other duties as determined by management.
Qualifications / Job Requirements:
* High school diploma / GED or an equivalent combination of education and work experience.
* A minimum of 1-3 years' experience working in a regulated environment, medical device or pharma/biotech quality management system (i.e., ISO 13485, ISO 14971, FDA 21 CFR Part 820) is preferred.
* Experience with incoming or in-process inspection, able to read and understand Engineering Drawings and Part Specifications.
* Experience participating in cross-functional teams to support business priorities is preferred.
* Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
* Able to use measuring equipment such as calipers, micrometers, gages, etc.
* Proficient in MS Office programs including Word, Excel and Arena is a plus.
* Strong understanding of quality control standards and testing techniques preferred.
* Result-oriented, positive 'can-do' attitude with demonstration of appropriate urgency and initiative.
Job Requirements
Compensation depends on experience but is typically 26-28/hr.
ABOUT KORE1
Specializing in professional and technical recruiting, KORE1 is committed to supporting top IT, Engineering, Creative, Scientific, Accounting and Finance professionals in their career paths. We build deep relationships with leading companies, connecting them to exceptional talent every day. With extensive industry expertise and unmatched opportunities, our goal is to provide a unique experience for our contractors and consultants as they prepare for their next role. We are passionate about matching the right people with the right companies.
Kore1 provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Kore1 complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Kore1 expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Kore1's employees to perform their job duties may result in discipline up to and including discharge.