Biomedical Engineering Jobs

Product Development Engineer (Becker Orthopedic Appliance Co,)

Fri, 17 May 2013 21:45:38 GMT

Job Title: Product Development Engineer
Company: Becker Orthopedic Appliance Co,
Location: Troy, MI

Becker Orthopedic, a leading manufacturer of orthotic components, and prefabricated bracing for patient care, is currently accepting resumes for a Product Development Engineer.

The successful candidate will possess:

- Baccalaureate or Masters Degree in Mechanical Engineering, Biomedical Engineering, or a related discipline
- Hands-on experience with elements of mechanical design, testing and product validation
- Strong organizational skills, with the ability to effectively achieve project milestones.
- Ability to collaborate with engineering, marketing and patient care - Familiarity with computer aided design (CAD)
- Competence with general computing, software, and hardware

Salary is commensurate with qualifications.

How to Apply:

EMAIL: jeberhardt@beckerorthopedic.net

FAX: 248-588-6961

To apply, please mail or fax (no phone calls please) your resume with cover letter to:

Julie Eberhardt
Human Resources
Becker Orthopedic
635 Executive Drive Troy, MI 48083
Fax: 248-588-6961

Or E-mail your resume and cover letter as body text (no attachments please) to: jeberhardt@beckerorthopedic.net

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Open Access Chromatography Engineering Technician (Yoh)

Fri, 10 May 2013 16:11:31 GMT

Job Title: Open Access Chromatography Engineering Technician
Company: Yoh
Location: Cambridge, MA

Yoh has a long-term contract opportunity for an Open Access Chromatography Engineering Technician to join our client, a world leader in the pharmaceutical industry, located in Cambridge, MA.

Job Responsibilities:

- Act as the primary support engineer for instrumentation within the Open Access labs of our Analytical Sciences and Chemistry departments.
- Keep instruments running at their optimum performance through proactive preventive maintenance.
- Monitor performance of equipment by implementing QC standard operating procedures.
- Work collaboratively with instrument users.
- Participate constructively in working teams and at lab meetings.
- Maintain spare parts inventory for commonly used replacements.
- Monitor trends in service requests and implement corrective actions to improve operational efficiency and reduce downtime of the instruments.
- Identify and report unsafe equipment, conditions and practices so that they may be corrected prior to an incident.

Job Qualifications:

- Ideally, the candidate would have two (2 - 5) years of experience in an industry setting as a Lab Technician (or BS) in a scientific discipline such as Biology, Chemistry, or Engineering.
- Ability to diagnose and remedy advanced hardware and software problems quickly.
- A basic understanding of HPLC (Prep and/or Analytical) techniques, instrumentation and underlying principles.
- Basic laboratory skills including preparing solvents, standards, and solutions preps.
- Strong PC skills in Windows 7 or XP OS.

Discover all that's possible with Yoh. Apply now.

Yoh is a professional staffing provider with over 70 years of experience in the short- and long-term staffing services industry; visit our website to learn both about our company and about our leading staffing solutions.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

How to Apply:

ONLINE: http://jobs.yoh.com/job/Cambridge-Open-Access-Chromatography-Engineering-Technician-Job-MA-02138/2582538/?feedId=975&campaignId=41&utm_source=EngineerJobs&utm_campaign=Yoh_ENG

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Biomedical Engineer/Clinical Specialist (Confidential)

Fri, 03 May 2013 15:09:44 GMT

Job Title: Biomedical Engineer/Clinical Specialist
Company: Confidential
Location: Atlanta, GA

High-tech medical company is seeking a Biomedical Engineer for a clinical specialist role to work with existing hospital relationships in the Atlanta area. Negotiable compensation package based on experience, education and prior compensation. Company will cover mileage, travel expenses, 401(k) and benefits. This is an excellent opportunity for someone who would like a more procedure-based clinical role that involves training and educating hospital staff on the applications.

2+ years of experience as a clinical specialist at a medical device/equipment company.
Associates or Bachelors Degree in biomedical engineering preferred.
High energy, personable, organized, attention to detail and excellent follow up skills.
Experience working with technical, capital equipment in a hospital setting ideal but not necessary.

The company will not consider candidates relocating to Atlanta.

How to Apply:

EMAIL: diane@friedmansearch.net

Please send an updated resume to Diane Roberts at diane@friedmansearch.net for consideration.

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Standards Compliance Engineer (Yoh)

Wed, 01 May 2013 17:21:54 GMT

Job Title: Standards Compliance Engineer
Company: Yoh
Location: Sunnyvale, CA

Yoh has a contract-to-hire opportunity for a Standards Compliance Engineer to join our client in Sunnyvale, CA.

Job Responsibilities:

- Read and understand detailed technical and regulatory documentation associated with complex electromechanical products.
- Work with Intuitive Surgical Engineering and Regulatory Teams, and external Certification Bodies, to assure that products meet the IEC 60601-1 3rd Edition standard, including risk management requirements.
- Review, modify and prepare the following for compliance with IEC 60601-1 and related medical device standards: Design History File documentation, Risk Management Files, Product Configurations, and Labeling.
- Meet deadlines on projects with specific goals and timelines.

Job Qualifications:

Required:

- Bachelors' degree in Engineering or related Science.
- At least five (5) years' experience applying medical device standards and regulations.
- Knowledge of risk management process for medical devices (ISO 14971).
- Knowledge of IEC 60601-1, Medical Electrical Equipment Requirements.
- Experience working with Certification Bodies (e.g., UL) to qualify products to international standards.
- Excellent communication and technical writing skills.
- Ability to work productively and proactively with technical, multi-disciplinary product teams.
- Strong organizational and work planning skills, detail oriented.
- Excellent problem solving/analytical abilities.
- Ability to manage multiple tasks in a time sensitive environment.
- Experience with use of a Project Lifecycle Management system (e.g., Agile) for document management and Engineering Change Orders.

Desired:

- Knowledge of requirements management tools(e.g., DOORS, MKS).

Discover all that's possible with Yoh. Apply now.

Yoh is a professional staffing provider with over 70 years of experience in the short- and long-term staffing services industry; visit our website to learn both about our company and about our Recruitment Process Outsourcing services.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

How to Apply:

ONLINE: http://jobs.yoh.com/job/Sunnyvale-Standards-Compliance-Engineer-Job-CA-94085/2555670/?feedId=975&campaignId=41&utm_source=EngineerJobs&utm_campaign=Yoh_ENG

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Senior Process Engineer (Yoh)

Wed, 01 May 2013 17:08:20 GMT

Job Title: Senior Process Engineer
Company: Yoh
Location: San Diego, CA

Yoh has a contract opportunity for a Senior Process Engineer to join our client in San Diego, CA.

Job Overview:

As a Sr. Process Engineer, you will drive and execute a project to identify and qualify a high-end, high-quality contract manufacturer or outsourced partner for the production of IVD-equivalent components. You will coordinate across disciplines and functions including R & D, Quality, Manufacturing, and other engineering groups to define requirements and execute to plan. You will act as liaison to the product team and communicate progress up to the executive level.

Job Responsibilities:

- Participate in process definition and improvement, design, development and quality test activities in the formulation, filling and packaging of reagents.
- Troubleshoot production line issues related to yield, purity, and TAT.
- Provide guidance for constructing and executing controlled experiments (including DOE's) to optimize processes, address yield and quality issues and drive implementation of solutions in a production environment to meet production goals.
- Analyze process test results, issues reports and make technical recommendations.
- Define technical requirements and write procedures for manufacturing to process product.
- Act as liaison, providing progress updates to the product team and senior management.

Job Qualifications:

- B.S./M.S. in Chemical or Bio/Biotechnical Engineering, or equivalent.
- Eight to ten (8 - 10) years of relevant experience in manufacturing support, sustaining engineering, process definition, design, scale-up, process improvement, and validation.
- Demonstrated expertise in GxP environment.
- Working knowledge and experience with clean room design, production and process controls, and process development.
- Experience with ISO 14644.
- Experience with ISPE, GHTF, ICH guidelines, and IVD directives is a plus.
- Experience with high volume manufacturing in a high tech, high volume consumables industry.
- Experience with sterilization process and cleaning validations.
- Experience with product development processes and project management.
- Good interdepartmental communication skills and documentation skills are required.
- Demonstrated ability to accomplish goals while working across departments is required.

Discover all that's possible with Yoh. Apply now.

Yoh is a professional staffing provider with over 70 years of experience in the short and long-term staffing services industry; visit our website to learn more about our company.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

How to Apply:

ONLINE: http://jobs.yoh.com/job/San-Diego-Senior-Process-Engineer-Job-CA-92101/2558487/?feedId=975&campaignId=41&utm_source=EngineerJobs&utm_campaign=Yoh_ENG

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Mechanical Engineer - Research (Yoh)

Wed, 01 May 2013 16:49:33 GMT

Job Title: Mechanical Engineer - Research
Company: Yoh
Location: Irvine, CA

Yoh has a contract position for a Mechanical Engineer - Research to join our client in Irvine, CA.

Job Responsibilities:

- Mechanical Engineer will be responsible for conducting research and design of experimental testing on bio-medical instrumentation and devices.
- Mechanical Engineer will also lead efforts in Protocol Development, Data collection, Analysis and Technical report writing.
- Other responsibilities include Test Setup and Competitive Testing.
- Perform routine Management of laboratory space and supplies

Job Qualifications:

- B.S. in Mechanical Engineering or Biomedical Engineering
- Minimum four (4) years relevant experience
- Hands on experience with test instruments
- Skilled with a microscope and video imaging
- Proficiency in SolidWorks, LabVIEW Software, MATLAB Software
- Proficiency in MS Word, Excel, Project, PowerPoint, Access

Preferred Qualifications:

- Advanced degree Mechanical Engineering or Biomedical Engineering
- Machine shop experience

Discover all that's possible with Yoh. Apply now.

Yoh is a professional staffing provider with over 70 years of experience in the short and long-term staffing services industry; visit our website to learn more about our company.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

How to Apply:

ONLINE: http://jobs.yoh.com/job/Irvine-Mechanical-Engineer-Research-Job-CA-92602/2560905/?feedId=975&campaignId=41&utm_source=EngineerJobs&utm_campaign=Yoh_ENG

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Manager - Instrumental Evaluation (L'Oreal USA)

Wed, 01 May 2013 15:24:11 GMT

Job Title: Manager - Instrumental Evaluation
Company: L'Oreal USA
Location: Clark, NJ

This position is in the Cosmetics Evaluation Group at L'Oreal USA's R&I facility in Clark, NJ.

This position is responsible for managing Cosmetics Aid-to-Formulation Instrumental Testing, Instrumental Methods Development and Instrumental and Consumer Claims-Substantiation Testing for all cosmetic products manufactured by LOreal USA.

Job Responsibilities:

� Guides team in developing new bio-instrumental and consumer claims tests and methods, as well as designing and conducting special study projects;

� Performs project tracking with resource/budget itemization;

� Develops and maintains an in-depth understanding of laboratory equipment and their capabilities, and ensures proper instrumental operation/maintenance documentation in instrumental master files;

� Evaluates and summarizes published literature on various topics in cosmetic testing;

� Maintains own and supervises teams laboratory notebooks to ensure they are up to date in accordance with standard operating procedures;

� Interacts with R&I marketing Liaison team, formulation labs and legal team to determine the instrumental and consumer methods for aid to formulation and product claims substantiation;

� Analyzes instrumental and consumer test data and writes reports to clearly communicate findings in a timely manner;

� Develops and scouts for new methods to establish novel instrumental and consumer cosmetic claims;

� Collaborates with French colleagues to standardize research protocols;

� � Works with consumers, expert panelists, cosmetologists, sensory & consumer scientists, formulators, French counterparts, clinicians, academics and consultants;

�� Forms ties to professional organizations and collaborates with colleagues in appropriate fields:

Requirements:

� Masters with 5 - 7 years or Ph.D. with 3 - 5 years of working experience with degrees in Biological or Physical Sciences, Chemical Engineering or Bio-Engineering or related fields;

� Excellent collaboration, interpersonal, presentation, written/oral communication skills in English, ability to communicate in French a plus;

� At least 3-5 years experience managing a team of diverse individuals engaged in scientific endeavors;

� � Working knowledge with demonstrated track record of innovation individually as well as leadership in a team setting;

� Specific knowledge and experience with skin bioengineering instrumentation and material/surface/interaction evaluations including optical/spectral, mechanical/viscoelastic, friction/force, surface energy, imaging/image analyses, as applied in cosmetics/consumer product industries are highly desirable;

� � Knowledge and experience using both parametric and non-parametric statistics, statistical modeling skills a plus;

� Creativity in developing new testing methods especially those used for cosmetic claims;

� Interview and survey-design skills a plus;

� Interest in human behavior/perception and sensory properties of products;

� Must be proficient in Word, PowerPoint, Excel. Expertise in data analysis and statistical software such as XLSTATS/SigmaSTATS, image-analysis and computational software such as MatLab, ImagePro , coding/programming skills highly desirable.

Must be legally eligible to work in the US on an on-going basis.

How to Apply:

ONLINE: http://www.aplitrak.com/?adid=amxhZGF5Ljg5NjMzLjQ5OTlAbG9yZWFsdXNhLmFwbGl0cmFrLmNvbQ

Source: Biomedical Engineering Jobs at Engineer Jobs.com

Medical Device Mechanical Testing Engineer (Empirical Testing Corp.)

Mon, 29 Apr 2013 15:08:00 GMT

Job Title: Medical Device Mechanical Testing Engineer
Company: Empirical Testing Corp.
Location: Colorado Springs, CO

Empirical Testing Corp., founded in 1998, www.empiricaltesting.com, and located in Colorado Springs, Colorado, is seeking an Engineer.

What We Do

Our employees are committed to providing the highest quality professional testing services for our customers, including accurate and reliable testing results, professional technical reporting, and a rapid response to any issues that arise. Above all, our services are designed to be sensitive to a fast-paced product development environment and are delivered at a competitive price.

Quality Assurance and Confidentiality

Empirical Testing Corp. is committed to Quality and Confidentiality. All employees must undergo training in both the QAS and confidential document handling. As a matter of course, all Empirical Testing Corp customer relationships are deemed confidential. The QAS ETC has implemented is based upon the requirements set forth by the most current version of ISO/IEC 17025. The QAS will meet or exceed these requirements and the requirements of the customers, by following ETC's established policies and procedures. This devotion to quality testing provides you with a competitive advantage by reducing costs, establishing credibility, improving efficiency, and enhancing profitability.

Medical Device Testing

At every opportunity, Empirical Testing Corp. deepens its commitment to performing the highest quality medical device testing. At present, ETC holds the widest range of accredited test standards for medical devices currently available in the United States and is dedicated to continually pursuing standards as they become available.

Good Laboratory Practices

By observing and utilizing Good Laboratory Practices (GLP), Empirical Testing Corp. assures integrity in lab planning, monitoring, recording and reporting.

Product Development Support

Empirical Testing Corp. is equipped to respond to a fast-paced product development environment. While our extensive scope of accreditation covers a wide variety of medical devices from spine to extremities, Empirical Testing Corp. is also dedicated to development and testing of custom protocols for devices that push the envelope of existing technologies.

Technical Reports

With a 24-hour operation and a team of knowledgeable biomedical engineers on-staff to help execute your test plan, ETC provides a complete service package, including an unsurpassed technical report, which is second to none. Our objective is to furnish you with accurate, reliable, test reports that can be submitted to meet global regulatory requirements, including FDA and CE marketing approval.

Commitment to the Profession

Our proven expertise in many biomechanical engineering disciplines, and our philosophy of continuous improvement in all that we do, enables us to be the "best in class. �At Empirical Testing Corp., we are committed to the field of medical device testing, which means you benefit from years of specialized bio-medical engineering experience, knowledge, and insight. From the moment you engage in a partnership with Empirical Testing Corp and throughout your product development cycle, you'll receive prudent suggestions, based on our experience and your test results, for turning your medical device concept into a product that meets regulatory marketing approval.

How to Apply:

EMAIL: samsargent@hrams.com

If you are interested in joining our team please respond with your resume, cover letter, salary history and requirements attention Sam Sargent. We offer a competitive compensation of base salary and bonus plus a competitive benefit package including medical, dental, life, and 401K match.

Source: Biomedical Engineering Jobs at Engineer Jobs.com