Specialist 2 – Quality Assurance (contract) job vacancy in JnJ – Jobs in California

Looking for a New Job? FINDTHETECH.COM is one stop place for searching new job openings.
We got a new job details in JnJ & they are Hiring Candidates for Specialist 2 – Quality Assurance (contract)

Job Details
Company Name :
JnJ
Company Location :
Redwood City, CA
Job Position :
Specialist 2 – Quality Assurance (contract)
Job Category :
Jobs in California

Job Description :
Johnson & Johnson
Title: Specialist 2 – Quality Assurance
Location: Redwood City, CA
Duration: 1 Year Contract
Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits

Please note that this is a contract role providing services to Johnson & Johnson through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be an employee of Johnson & Johnson.

Summary:
The Quality Assurance Inspector is responsible to provide general quality assurance support in the areas of inspection, document control and the overall maintenance of the quality management system. This position supports both R&D and Operations through all phases of product lifecycle. The candidate will utilize SAP to document Quality transactions as well as assist in compiling and trending quality data.

Responsibilities:

Performs Quality review of documents related to QC testing, receiving inspection and lot history records (LHR) or device history record (DHR) as required.
Verifying product meets specifications and provide final quality approval
Initiate and process Non-Conforming Material Reports when required and documenting non-conformance to specifications through the completion of required paperwork, SAP system transactions.
Understanding of QSR/ISO 13485, 21 CFR 820, GMP environment and document results per GDP standards
Supporting and participating in internal and external audits such as Notified Body and FDA as needed.
Performs incoming and in-process inspection of products as needed.
Assists in developing and implementing effective inspection to verify compliance of product with specifications.
Assists in developing inspection requirements and sampling plans for components and performs inspection activities as required.
Perform inspections of purchased parts, subassemblies, or finished company products according to specifications or standards using standard physical, mechanical and/ or electrical measurements as needed.
Accurately document the results of the inspections and testing in SAP and on data sheets/forms as applicable.
Maintaining all controlled document files and test records in a timely and accurate manner.
Participate and/or assist in writing and updating inspection procedures, protocol, and checklists.

Qualifications:

Minimum HS diploma and practical experience. AA or AS degree preferred.
Knowledge of GD&T preferred
3+ years Quality Assurance and Quality Control experience preferred.
Working knowledge of the FDA medical device Quality Systems Regulations and international quality system standards QSR/ISO 13485 and 21 CFR 820.
Ability to read and comprehend engineering drawings and schematics is preferred.
Ability to work independently, prioritize activities and communicate well.
Proficient in analytical, written, oral communication skills; and the ability to manage a variety of tasks simultaneously within cross-functional teams under minimal day-to-day supervision.
Proficient technical writing skills and use of documentation programs (e.g., Office Windows, Excel, Access, Power Point, etc.).
Able to identify and recommend effective solutions to problems, utilizing technical problem-solving tools, working individually and with others within and outside the quality function.
Previous experience with SAP preferred
Proficient in knowledge of a variety of testing equipment (including Instron, pin gages, snap gages, micrometer, caliper, etc.) is helpful.

Work Environment
This position operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.

This is a full-time position. Days and hours of work are flexible Monday through Friday, generally 8:30 a.m. to 5:30 p.m. Occasional evening and weekend work may be required as job duties demand.

Disclaimer : We are just publishing information regarding new job openings and not legally responsible for any Post. Candidates are requested not to pay any money to anyone posing as FINDTHETECH.COM

Similar Posts

Leave a Reply

Your email address will not be published.