better Quality Assurance Job at Health Care Products

Embedded Software Test Engineer Requisition ID 31580 Full/Part Time x Location Valencia CA Description Primary Function Systems and Software Test Group Embedded FW Test Development Duties and Responsibilities Designs, develops, and implements testing methods and equipment for evaluating standard and special devices using state of the art tools and test automation programming techniques. Frequent use and application of technical standards, principles, theories, concepts and methods. Provide solutions

Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Champion of Quality System design whose responsibilities include,

Job Title Quality Engineer - Integrated Manufacturing Division Stryker Instruments Location (Country - State) United States - Michigan City or Sales Region Kalamazoo Business Function Manufacturing/Operations Shift 1st Education and/or Special Training B.S. in Mechanical or Electrical Engineering or related curriculum. Job Description The Quality Engineer will develop, execute, and maintain Stryker's Quality Systems to comply with regulations from the FDA and other international regulatory bodies for the design

Job Title Contract Validation Engineers Division Stryker Instruments Location (Country - State) Ireland City or Sales Region Cork Business Function Manufacturing/Operations Shift N/A Education and/or Special Training EDUCATION/TRAINING REQUIRED: . A Bachelors or Masters Degree in an engineering discipline. . Minimum 3 years experience in a manufacturing or production engineering environment. Job Description RESPONSIBILITIES: The successful candidate will be responsible for supplier manufacturing related activities

Requires Bachelor s degree in Engineering 3 years experience in a quality assurance role within a manufacturing environment...

Requires Bachelor s degree in Engineering 3 years experience in a quality assurance role within a manufacturing environment...

Job Title: Senior Systems Verification Engineer Location: St. Paul - MN - USA Job Category: Software Engineering Shift: 1st Date Posted: 11/13/2009 Description: St. Jude Medical develops medical technology and services that focus on putting more control into the hands of those who treat cardiac, neurological and chronic pain patients worldwide. The company is dedicated to advancing the practice of medicine by reducing risk wherever possible and contributing to successful outcomes for every patient. Headquartered

Job Title Quality Assurance Engineer II Location St...Paul MN USA Job Category Quality Assurance Quality Shift 1st Date Posted 11 02 2009 Description St...5 years of experience in a quality assurance role within a manufacturing environment...

Location Minnetonka MN USA Job Category Quality Assurance Quality Shift 1st Date Posted 10...

Sr Test Engineer Requisition 69644 Category Engineering Business Cardiac Rhythm Disease Mgmt Division Microelectronics Location USA-AZ-Tempe Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage less than 10% Experience Required 5 years Education Required Bachelor of Engineering Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description Develop and support Hybrid Test Solutions (Multi-Chip Module) for

material science 7 10 years of quality assurance engineering experience demonstrated skills in Statistical...Lean Six sigma skills 7 10 years of quality assurance with Master Degree in a related field...

years of experience in the Software Quality Assurance or Software Development field Experience with...

The Quality Assurance Complaint Analyst is responsible for timely investigation of safety information related to LifeCell s marketed products...

Exactech, Inc. is an orthopaedic company that develops, manufactures, markets, distributes and sells orthopaedic implant devices, related surgical instrumentation and biologic services to hospitals and physicians in the United States and internationally. RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO: 1. Perform and document inspection requirements following approved SOP s for incoming, in process, OEM and finished products. Document and notify QA Supervisor of non-conformances. 2. Status products

Stryker is an exceptional company with exceptional people who deliver exceptional results. We have differentiated ourselves by advancing meaningful innovations, creating cost-effective solutions for and improving the lives of our global customers and patients. As a winner of the 2007 and 2008 Gallup Great Workplace Award, we have demonstrated that Stryker has one of the most productive and engaged workforces in the world. Our exceptional results fuel ongoing opportunities for Stryker employees to build outstanding

Southborough MA The Quality Assurance Manager will drive exceptional product quality...EOE M F D V Manage 2 3 employees in the OEM Quality Assurance and Quality Control areas...of experience in Manufacturing Engineering or Quality Assurance is required...

Company: Siemens Medical Solutions USA, Inc. Division: SMS - Ultrasound Division Location: WA - Issaquah Req ID: 83839 Position Title: Software Test Engineer 1 Experience Level: Entry Level Education Required: Bachelors Degree Travel Required: No Company Description: We are one of the largest global suppliers of healthcare equipment, renowned for innovative products, services and solutions including diagnostic imaging systems, therapy equipment for treatment and electromedicine and IT solutions to

to the Director of Quality the Quality Assurance and Process Control QAPC Manager is...Job Title Manager Quality Assurance Medical Device Pharmaceutical Req 5255BR Job...Responsible for providing strategic and tactical leadership for the Quality Assurance and Process Control Department...

Sr Quality Engineer Requisition ID 31523 Full/Part Time x Location Spencer IN Description PURPOSE: Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, and communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support operational

cases Ensure that products are appropriately quality assurance tested Utilize strong ability to communicate...

Knowledge Industrial Quality Control Quality Engineering Quality Assurance and Validation...

Provide Quality Assurance approvals for Specification Design Review and...

Quality Assurance Associate within our NovoCart Division...Facilitates the establishment of new product specifications and process and product improvements with Quality Assurance Manager...Represents Quality Assurance in design review and new product development...

Company: CAPS Requisition #: 1508 Job Title: Quality Regional Manager (OH, NY, CT, MA region) State: Connecticut City: Wallingford Job Description: Central Admixture Pharmacy Services, Inc. (CAPS), a subsidiary of B.Braun Medical Inc., is a state licensed pharmacy also operating as a manufacturer registered with the FDA. CAPS services originate from a free-standing facility with a focus to provide daily admixing and delivery of parenteral drugs, solutions, and nutrition. We are currently seeking a QA Regional

Company: B.Braun Requisition #: 1540 Job Title: Quality Engineer State: California City: Irvine Job Description: Since its founding in 1839, B. Braun has built an unparalleled store of knowledge and expertise in delivering innovative healthcare products, medical devices and programs that enhance working processes in hospitals, alternate care settings and medical practices - increasing safety for patients, doctors and nurses. Its 38,000 employees worldwide are proud of their commitment to translating customer

Five 5 years of experience in quality assurance in the pharmaceutical or medical device...and control of microbiology and sterilization quality assurance programs for B Braun to ensure...Essential Functions Manage Quality Assurance Program and project deliverables for R...

Knowledge Industrial Quality Control Quality Engineering Quality Assurance and Validation CFR s and their...

Company: CAPS Requisition #: 1617 Job Title: Quality Control Coordinator State: Maryland City: Lanham Job Description: We are currently seeking a Quality Control Coordinator for our Lanham, MD facility. The QCC is responsible for monitoring and documenting compliance with the CAPS Continuous Quality Assessment and Improvement Program within each CAPS pharmacy. Qualified candidates will possess: B.S. or B.A. degree in Science (Biology, Microbiology, Chemistry, Pharmacy). Minimum of 2 years experience in a QA

Job Title Quality Assurance Analyst Division Stryker Orthopaedics Location Country...

May train others in Quality Assurance GMP FDA QSR related topics...

City Carlsbad State CA Job Title Respiratory - Sr Validation Engineer - Enviornmental / Safety (09-0686) Description Covidien is a nearly $9 billion global leader in medical devices and supplies, diagnostic imaging agents, pharmaceuticals and other healthcare products. For decades our brands have defined their categories in the healthcare field, and today we support the lifesaving work of medical professionals in more than 130 countries. Covidien is 42,000 employees in 57 countries, who are passionate about

Manage and direct in plant Quality Assurance operations...Provide organization and direction to the Quality Assurance department team 12...experience in a FDA regulated industrial Quality Assurance environment...

City Carlsbad State CA Job Title Respiratory - Senior Quality Engineer Description Nellcor Puritan Bennett, is now the Respiratory and Monitoring Solutions (RMS) business unit of Covidien, formerly Tyco Healthcare. RMS systems are used to monitor, diagnose and treat respiratory disease and sleep disorders, and they provide life sustaining ventilation and oxygen support for patients. In addition to Respiratory and Monitoring Solutions, Covidien also manufactures, distributes and services a diverse range of industry

Quality Audit Engineer The Quality Audit Engineer performs detailed audits of practices at all company locations to ensure that policies and procedures comply with guidelines set forth in the Food and Drug Administration (FDA) manual and other applicable regulations. Reports on weaknesses, ineffective procedures, policy exceptions, and reporting discrepancies and recommends appropriate corrective actions. The Quality Audit Engineer consults with management to establish practices and procedures that comply

for the management of the Clinical Quality Assurance function in assigned business area s...trains supports and develops junior Clinical Quality Assurance staff Auditors and Specialists Performs and...and the appropriate regulations for Clinical Quality Assurance Ensures all employees are trained to...

The Director will provide leadership and functional oversight to the Clinical Quality Assurance and Pre Clinical Quality Assurance Groups...the implementation of the Global clinical quality assurance audit programs to access GCP and...General Summary The Director of Clinical Quality Assurance QA will focus on the implementation...

Description It is the responsibility of the Senior Quality Engineer to provide expert guidance on product design and processes as they relate to compliance with quality system requirements. 1. Provide focused quality engineering support and assume responsibility for timely and effective coordination and/or execution of assigned development project activities. 2. Qualify suppliers and monitor their performance. 3. Track quality trends and initiate action items to resolve issues. Manage assigned corrective

SUMMARY DESCRIPTION Directs and participates in quality assurance efforts to ensure that the Company...SUPERVISION RECEIVED Under direct supervision of Director of Quality Assurance...Generates and maintains quality assurance standards procedures and controls...

support group 1 years in a quality assurance group Basic knowledge of Linux operating...

in areas of process engineering product quality assurance and quality engineering to drive continuous...Lead the product quality assurance and quality engineering aspects of activities...Establish quality assurance engineering programs and initiatives to ensure...

Detailed knowledge of embedded software development quality assurance and verification and validation testing In...

Transforming the hearing care industryStarkey is a recognized world leader in high quality audio technology. We serve our customers by providing a broad range of hearing devices that meet a variety of hearing needs. Through unsurpassed customer service practices, we strive to bring a human touch to hearing healthcare. The Starkey Laboratories family of companies includes Audibel, Micro-Tech, Nu-Ear, and Starkey. Starkey is an Equal Opportunity Employer. Do you want to work for a cutting edge medical device

and risks and the development of quality assurance practices and controls in new product...new product development needs Conduct software quality assurance plan audits to verify development practices...quality assurance engineers and inspectors Handle quality assurance engineering responsibilities after launch Prepare risk...

Sr. Software Quality Engineer Requisition ID 31504 Full/Part Time x Location Spencer IN Description PURPOSE: Develops, establishes and maintains software validation quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate software validation quality goals and priorities. Provides

Location Beaverton OR OR Department Manufacturing Quality Assurance Relocation Provided Yes Education Required Bachelors...

City North Haven State CT Job Title QA ENGINEER Description Performs Quality Engineering functions including: design verification (Design for Six Sigma), reliability engineering, component specification / approval, process evaluation and nonconforming product analysis in a project team environment. Evaluate component and sub-assembly subcontractors to ensure device quality and conformance to standards and regulations. Ensures that components and finished devices are properly specified and inspected, and the

City Mansfield State MA Job Title Sr. Design Quality Engineer Description SUMMARY OF POSITION: Leads the Quality Engineering function within new product development including: design for Six Sigma, reliability engineering, component specification / approval, process evaluation and nonconforming product analysis in a project team environment. Evaluate component and sub-assembly subcontractors to ensure device quality and conformance to standards and regulations. Identifies, qualifies, and implements inspection

Description Develops implements and maintains technical quality assurance systems and activities Function Quality Division...

SUMMARY OF POSITION Supervises the overall Quality Assurance Inspection and Sterilization operations...This position will provide technical support to all of Quality Assurance inspection regarding training and interpretation of Quality Procedures...

Manage and direct in plant Quality Assurance operations...ORGANIZATIONAL RELATIONSHIPS SCOPE Position reports to corporate Quality Assurance Director...