better Quality Assurance Job at Medical Devices

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

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...

Position Responsibilities Support test development and production support efforts for Mixed Signal Hybrid Multi chip Module Implantable Medical Devices...

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...

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

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

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...

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...

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...

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

the responsibility and authority to provide Quality Assurance Engineering representation to select business teams...assure the design and production of medical devices are in compliance with applicable standards...

Acts as an advisor on clinical quality assurance issues such as patient informed consent...

Job Title: Quality Control Tech II Location: Portland - OR - USA Job Category: Quality Shift: 2nd Date Posted: 11/04/2009 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 in St. Paul, MN, St.

Location Minnetonka MN USA Job Category Quality Assurance Shift 1st Date Posted 11 03...

Job Title: QA INSPECTOR II Location: Minnetonka - MN - USA Job Category: Quality Control Shift: 1st Date Posted: 11/03/2009 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 in St. Paul, MN, St

Quality Engineer Manager Industry Title /Category: Quality Engineer Manager/Engineering Job ID: 2009-3945 Standard Title: Quality Engineer Manager Career Level: experienced Location/Division: Covington, GA/Bard Medical Relocation: yes Posted Date: 11/2/2009 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11

Sr Clinical Quality Assurance Specialist Requisition ID 31463 Full Part...Assists the Manager CQA with internal quality assurance program for the assigned business area...schedules and conducts internal and external quality assurance audits of the systems procedures and...

Quality Manager II -Post Market Surveillance-31454 Requisition ID 31454 Full/Part Time x Location Natick MA Description The Manager II, Corporate Post-market Surveillance will report directly to the Director, Corporate Post-market Surveillance and provide leadership, corporate oversight, and subject matter expertise for BSC complaint handling and world-wide regulatory reporting policies, procedures, and associated electronic systems. This includes but is not limited to setting and executing the vision,

Supports quality assurance activities by maintaining sterilization standards for all Smith Nephew products...Must have experience working within a regulated environment medical devices etc...

Job Title: Quality Control Inspector I Location: Irvine - CA - USA Job Category: QA Administration Shift: 2nd Date Posted: 06/05/2009 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 in St. Paul

Job Description: The Manager II, Corporate Post-market Surveillance will report directly to the Director, Corporate Post-market Surveillance and provide leadership, corporate oversight, and subject matter expertise for BSC complaint handling and world-wide regulatory reporting policies, procedures, and associated electronic systems. This includes but is not limited to setting and executing the vision, goals, metrics, and work standards for the management team to work cohesively and effectively. The role also

Quality Engineer Bovie Medical Corporation, a progressive medical device manufacturer located in Clearwater, FL. Bovie Medical is setting the standard for surgi-center and hospital-based electrosurgical generators and accessories with a range of state of the art' models: the Aaron 800-EU, the Aaron 900, the Aaron 950, the Aaron 1250, the Aaron 2250, and the Aaron 3250 along with the IDS-200, IDS-300, and ICON Gi. This full line is the most complete offering of any USA manufactured electrosurgical generator

Incoming Quality Inspector Industry Title /Category: Medical Device/Advanced Quality Engineering Job ID: 2009-3935 Standard Title: Incoming Quality Inspector Career Level: experienced Location/Division: Warwick, RI Relocation: No Posted Date: 10/27/2009 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000

Engineer Industry Title Category Medical Device Quality Assurance Job ID 2009 3931 Standard Title...

Biomet offers excellent compensation health care and retirement benefits...

be responsible for developing and maintaining quality assurance systems and records for all Orthopaedic...

Quality Engineer Requisition ID 31393 Full/Part Time x Location Cork CORK Description JOB PURPOSE: Act as a member of the Boston Scientific Cork facility Quality Team. To provide expert QA support to Operations, in ensuring operational goals and objectives are achieved for the plant Key Responsibilities: Drive and implement process improvements to ensure predictable processes across all product lines (e.g. Risk Reduction, Yield improvements, Customer complaint reduction, Error proofing, Cost Reduction

Individual projects may be assigned to address a specific area of Quality Assurance...

ID 2009 3928 Standard Title Manager Quality Assurance Career Level experienced Location Division Moncks...Manager Quality Assurance Industry Title Category Manufacturing Medical Device...products is currently seeking a Manager Quality Assurance to join our Quality team in...

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

THIS IS A GREAT OPPORTUNITY TO JOIN OUR GROWING COMPANY!!!! Orthovita, Inc. located in the Great Valley Corporate Center in Malvern, PA. We are a biomaterials company with proprietary technology for the development and commercialization of synthetic, biologically active, tissue engineering products for orthopedic and neurosurgical applications. We are currently expanding in our Quality Department and looking for a QUALITY SPECIALIST to join our growing team. SUMMARY OF FUNCTIONS: Responsible for

Quality Engineer Requisition 68462 Category Engineering Business Spinal a Biologics Division MSB-Operations Warsaw Location USA-IN-Warsaw Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage 0% Experience Required 2 years Education Required Bachelors Degree Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description Responsible for developing and maintaining systems for insuring Quality of products produced

pharmaceutical development project team with the quality assurance deliverables including but not limited to...

- - Edwards Lifesciences is the global leader in the science of heart valves and hemodynamic monitoring, with more than five decades of experience in partnering with clinicians to develop life-saving innovations. Headquartered in Irvine, Calif., Edwards treats advanced cardiovascular disease with its market-leading heart valve therapies, and critical care and vascular technologies, which are sold in approximately 100 countries. The company has more than 6,200 employees worldwide

products over the counter drugs OTC medical devices and cosmetics...Must have experience working within a regulated environment medical devices etc...

Principal Quality Engineer Tracking Code 1482 Job Description Primary Functions Resolve quality and reliability issues through team-based problem solving activities. Supports product and process inspection activities by ensuring adequate inspection criteria and methodologies are in place across operations. Coordinates the review and revision of specifications and inspection instructions. Works on improving quality systems and completing CAPAs. Provide quality engineering support to production, receiving inspection

Acts as an advisor on clinical quality assurance issues such as patient informed consent...

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

Quality Assurance Ensures approved methods and procedures for...and international quality system requirements for medical devices...products to ensure adherence to internal quality assurance requirements...with specialization to include quality control quality assurance quality engineering and regulatory affairs...

Quality Engineer Requisition ID 30778 Full/Part Time x Location Galway GALWAY Description Job Purpose Demonstrates commitment to the Quality Policy (patient safety and product quality) through their daily execution of sound quality practices and the maintenance of an effective quality system. . Understands and complies with all the regulations governing the quality systems Ensures their direct reports are aware of their commitment to patient safety and product quality, are current with their training

Responsibility and Authority The Director of Quality Assurance has the authority and responsibility for...Director of Quality Assurance Responsibility and Authority The Director of...and maintains the budget for the Quality Assurance Department Develops implements and coordinates through...

Education Training B S in Electrical Engineering Quality Assurance or Life sciences or equivalent experience is required...

Senior Verification Engineer will be a member of a team that is responsible for development and verification of a complex, multi-tier, web application based on J2EE framework. Working without appreciable direction, the candidate will perform software testing duties that involve devising verification strategies, analyzing functional and non-functional requirements, producing test plans, and executing test cases. Required Qualifications: - 5+ years testing an external facing, database driven internet application