QA Associate II jobs in United States
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BD · 1 day ago

QA Associate II

BD is one of the largest global medical technology companies in the world, dedicated to advancing the world of health. The QA Associate II is responsible for quality inspection and control on manufacturing production lines, ensuring compliance with GMP and GDP standards, and performing various inspections and analyses to maintain product quality.

Health CareMedical DeviceTechnical Support
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Independently perform and document final inspection of all production slides, vials, kits, and labels to established quality specifications, and make independent determination of acceptability for release
Independently perform incoming inspection of a wide variety of materials, analyze inspection results versus specifications, ensure correct sampling plans are used
Work with production associates to ensure materials utilized are released and correctly accounted for, line verification is performed prior to start of production, verify accuracy and completeness of documentation, and confirm equipment used meets designated specifications including calibration
Work with manufacturing personnel to accurately complete required Quality Control (QC) testing, documentation and determine correct disposition
Detect nonconforming conditions during inspection and accurately document each condition. Demonstrate a bias for action to determine scope of nonconforming conditions, and segregate nonconforming products to prevent further use
Perform basic lab support functions, including preparation of basic standards and reagents, PM, 5S, and cleaning and handling of hazardous waste as appropriate
Responsible for maintenance of retention samples, and electronic and physical storage of device history records
Must perform work in a safe manner adhering to gowning and PPE procedures
Participation in continuous improvement activities is required (e.g. kaizen)
Additional responsibilities as assigned by management

Qualification

Quality Control (QC)FDA regulated environmentSAPMicrosoft OfficeSampling techniquesObservation skillsCritical decision makingRisk assessmentBasic validation knowledgeEquipment calibrationAttention to detailIndependent work

Required

High School Diploma/GED with a minimum of 2 years related QC or manufacturing experience
General Proficiency in Microsoft Office
Demonstrated understanding of sampling techniques and inspection standards
Basic math skills and the ability to utilize Excel for basic calculations and graphing
Must be able to speak, read, and write English fluently as well as write technically and summarize information into data reports using Microsoft Word
Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations
Excellent observation skills with a bias for 'corrective action' and improve work environment processes and procedures
Demonstrated ability to make critical decisions regarding product quality or quality system compliance
Ability to assess and articulate risk when evaluating a situation
Knowledge of basic validation, equipment calibration, and change requirements
Demonstrated understanding of the use of calibrated equipment
Proven capability to prioritize responsibilities and complete tasks on schedule
Must be able to work independently in a fast-paced manufacturing environment
Ability to stand for long periods of time
Ability to lift 25 lbs
Ability to do repetitive motion

Preferred

Basic knowledge of SAP is preferred
Experience working in an FDA regulated environment is highly desirable

Company

BD helps advance clinical therapy with the process for patients and health care providers with innovative technology services and solutions.

H1B Sponsorship

BD has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (66)
2022 (4)
2021 (3)

Funding

Current Stage
Public Company
Total Funding
$540M
Key Investors
Steris
2023-08-02Post Ipo Equity· $540M
1962-04-23IPO

Leadership Team

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Tom Polen
Chairman, CEO and President
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Richard Byrd
Executive Vice President and President of the BD Interventional Segment
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Company data provided by crunchbase