Mechanical Engineer. If interested, please submit your resumes to

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1 The Foundry is the premier medical device company incubator for inventors to rapidly transform their concepts into companies. The Foundry team has founded and financed ten medical device companies since its inception in 1998, and those ten device companies employ over 300 people today. Attached you will find a brief summary of the Foundry portfolio companies that are actively recruiting, along with positions available within those organizations. This may be the opportunity you have been seeking -- to join a broad network of creative, proven professionals. To learn more about The Foundry or any of our portfolio companies, please visit us on the web at The Foundry, Inc. is an Equal Opportunity Employer.

2 Cabochon Aesthetics, Inc., a spin-off of The Foundry ( is an emerging start-up company located in Menlo Park. Developed by leaders in the medical device industry, we are dedicated to developing effective scientific solutions for aesthetic procedures. The investors of Cabochon Aesthetics include Split Rock Partners, Morgenthaler and Prospect Ventures. This is a rare opportunity to join a dynamic team of creative professionals with a proven track record of success. Cabochon Aesthetics, Inc. is an Equal Opportunity Employer. Mechanical Engineer We are currently looking for a bright, motivated mechanical engineer with 3-5 years experience in mechanical design and development of multi-component systems to be an integral part of our team. The ideal candidate will have expertise in SolidWorks, demonstrated skills in rapid prototyping, and a knack for devising innovative solutions. Bachelor s degree or equivalent in Mechanical Engineering or similar discipline required and basic machining skills would be an additional plus. The primary responsibilities of this position include design and integration of mechanical elements with the rest of the system. You will have the opportunity to work with a small, highly-skilled group of engineers and other professionals in the medical device field. We offer competitive compensation and benefits, including stock options, an exciting and collaborative work environment, along with an excellent opportunity for career growth. If interested, please submit your resumes to bmacintosh@cabochoninc.com.

3 Concentric Medical Inc. is a medical device company committed to opening the pathway to stroke treatment. We are the first company to complete a pivotal trial and receive FDA clearance for a device for the removal of blood clots from patients experiencing an ischemic stroke. The Merci Retriever is a novel therapy that removes the clot, restores blood flow and offers hope for ischemic stroke patients with no other options. Founded in 1999, the company has gathered together a dynamic team of medical professionals, engineers, clinicians and employees in Mountain View, CA to deliver our commitment to opening the pathway to stroke treatment. The company is working hand in hand with stroke centers to provide new options for stroke treatment and develop new solutions to make a difference in the lives of stroke patients. Please submit resumes to hr@concentricmedical.com. Concentric Medical, Inc. is an Equal Opportunity Employer. Career Openings

4 Evalve was incorporated in 1999 to design, develop, manufacture and market innovative devices to enable percutaneous repair of cardiac valves. The company s initial products are intended to reduce the risks, trauma and costs associated with current open, arrested heart surgical options. The company s present development and clinical efforts are focused on mitral valve repair. An estimated 4 million people in the United States have significant mitral valve insufficiency, with an annual incidence of 250,000. Approximately 50,000 of these patients undergo surgery each year. Valve insufficiency, if left untreated, is associated with chronic volume overload, which ultimately leads to atrial fibrillation, heart muscle dysfunction, symptoms of congestive heart failure (CHF) and an increased risk of sudden death. Improved treatment options for people with valvular insufficiency may reduce the potential for developing CHF and may improve the quality of life for those currently suffering from CHF. Evalve, Inc. is an Equal Opportunity Employer. Positions Available: Sr. Manufacturing Engineer The Sr. Manufacturing Engineer designs and develops manufacturing processes, tooling and fixtures in order to meet daily production schedules, while enhancing productivity and product quality. Designs and develops manufacturing processes for new products, product changes and enhancements and related tooling and fixtures which are consistent with a zero defect level as well as low product cost. BSME, MSME preferred. BS and 8-12 years of experience, or MS and 6-10 years of medical device experience. Manufacturing Engineer II Designs and develops manufacturing processes, tooling and fixtures in order to meet daily production schedules while enhancing productivity and product quality. Create and maintain tool drawings and shop orders in coordination with the Quality Assurance and R & D functions. Position requires a BSME or MSME with 2 to 5 years of experience. Quality Assurance Inspector Perform inspections, checks, tests, and sampling procedures of incoming materials, parts and components used in the manufacture of medical devices. High School graduate equivalent required. AA in a technical field preferred. Minimum of 1-2 years experience in manufacturing required. Sr. Quality Assurance Technician Support incoming inspection and production quality control activities. Provide guidance to technicians, assemblers, and engineers in accordance with Evalve internal policies and procedures. Responsible for assuring that components, subassemblies and products have been manufactured, inspected, and tested using approved procedures and specifications. Investigate and initiate process improvement initiatives. High School diploma required; AA (or some college) in a technical field preferred. 6 plus years of QA/QC experience required.

5 Quality Assurance Specialist Implement, support, and sustain elements of Evalve s quality system through procedure generation, training, auditing, and technical support. The quality specialist serves as a key resource for maintaining compliance to ISO, EN, MDD, and QSR requirements. Must be able to provide and implement solutions to decisions related to product quality and compliance. The position requires a bachelor s degree (or equivalent QA/QC medical device experience) in engineering or life sciences and 3 5 years of experience in the medical device industry. Associate Marketing Manager The Associate Marketing Manager will be responsible for executing various marketing activities to support clinical studies of Evalve s percutaneous valve repair technologies and to support commercial launch of approved products. The individual will be specifically responsible for assisting in the development and fulfillment of media communications including print, video, and internet to increase enrollment and launch products. BS/BA in communications or marketing preferred. Video/graphics development/editing experience also preferred. Production Supervisor Supervise the activities of assemblers in the production area: schedule, train, motivate and evaluate employees. Participate in developing new procedures and processes needed to improve manufacturing or to introduce new products. Ensure that daily production schedules are met, and that manufacturing standards and procedures are followed. The position requires a High School diploma but an AA degree or some college is preferred. Four or more years of experience, preferably in a medical device company is required. Clinical Data Associate The Clinical Data Associate will perform duties associated with the processing, tracking and monitoring of data for a highly controlled clinical trial. Job responsibilities include data entry, maintaining clinical databases, communicating with Clinical Site Personnel, reviewing medical data for safety and effectiveness endpoints, performing data analysis and preparing presentations for Industry conferences supporting the clinical trial enrollment process. A Bachelors degree in science is preferred with a minimum of one years experience in the medical device industry. If interested, please submit your resume to hr@evalveinc.com.

6 Miramar Labs, Inc., the newest portfolio company from The Foundry, is an early-stage medical device company. Miramar is developing electromechanical solutions to serve a significant market opportunity. The culture is dynamic, demanding and fun. We seek experienced, driven individuals who take personal responsibility for the achievement of results. If interested, please submit your resume to info@thefoundry.com. Miramar Labs is an Equal Opportunity Employer. Positions Available: Manager / Director of Clinical Affairs Plan, develop, and implement Company policies, procedures, practices, and strategy for the Clinical Affairs function in support of efforts of R&D and Sales & Marketing. Responsibilities: Develop and implement clinical research strategy for all studies on investigational devices and manage those programs. This will include preclinical, clinical and post-market studies. Work with marketing management to choose investigators and clinical sites. Serve as the primary interface with clinical investigators and IRBs. Design clinical studies based on input from internal sources and investigating physicians and statisticians. Manage the generation of clinical protocol, documentation, data management tools. Negotiate contracts with hospitals, consultants and clinical investigators, core labs, contract research organizations, and database management firms. In conjunction with Marketing, develop and oversee Company physician training programs. Collaborate with the Research and Development, Manufacturing, and Marketing functions to develop product development strategy from product inception through product launch. Participate in the short and long range planning of new product opportunities. In conjunction with Marketing, manage the preparation of technical and scientific publications, including identifying and managing clinical authors, identifying target societies, meetings and journals. Qualifications: Bachelor s Degree in biostatistics or life sciences or equivalent experience required. Background in epidemiology, biostatistics or advanced degree is a plus. Minimum seven to fifteen years related experience in the medical device industry in addition to at least three years of supervisory experience. Experience in clinical study design, management, and analysis is also required. Document Control Clerk (Part-Time) Review quality documentation for completeness (e.g., ensure forms are completed and signed) Process documents and records, including limited word processing, soft and hard copy filing, and data entry File maintenance, including auditing for accuracy and completeness Work with engineering and management level staff to receive, route, process, and distribute documentation as required

7 Manufacturing Engineer As the first member of the manufacturing group, the candidate will support the product development team in transitioning products from prototype to production. Qualified candidates should be skilled problem solvers through the application of scientific methods. Responsibilities: The manufacturing engineer will be responsible for performing the following activities: Supervise and support ongoing manufacturing operations including supervision of assemblers Develop manufacturing equipment and fixtures Identify and implement process improvements to improve quality and yield Assist R&D team in implementing design-for-manufacturability features into the product, including design of injection and over-molded components Train operators, technicians, and engineers on use of equipment and fixtures Design and perform process validations Qualifications: Minimum BS degree in mechanical or industrial engineering or equivalent Minimum 5 years of medical device industry experience Experience with electro-mechanical devices or energy delivery devices preferred Excellent communication skills Hands-on and comfortable in a fast-paced start-up environment Pre-Clinical Research Scientist/Engineer The Pre-Clinical Research Scientist/Engineer is an essential member of the product development team. Under the guidance of the head of Research and Development, the candidate will be accountable for the design, development, execution, and reporting of in-vivo and ex-vivo pre-clinical experiments. Responsibilities: Support R&D pre-clinical product feasibility, development, and research efforts Work with development teams to design, coordinate, and execute pre-clinical studies Work closely with clinical department in integrating pre-clinical data with clinical data in support of regulatory submissions and marketing strategies Coordinate and schedule pre-clinical studies with outside study facilities Prepare pre-clinical test protocols and reports Collect, organize, analyze, and report pre-clinical outcome data Participate in cross-functional meetings Qualifications: BS in life sciences, engineering, or equivalent preferred. Experience in the medical device industry highly desirable. Experience with pre-clinical animal studies is highly desirable Excellent verbal and written communications skills Strong interpersonal skills Demonstrated problem solving skills Demonstrated outstanding organizational abilities Team oriented

8 Satiety, Inc. is the fifth portfolio company from The Foundry. Satiety is an early-stage company with strong venture capital backing that is developing minimally invasive devices to treat obesity and certain other gastrointestinal conditions. The company s first product is in an early stage of clinical investigation, with very positive results so far. This is your opportunity to join a dynamic team with a proven track record of success. Satiety, Inc. is an Equal Opportunity Employer. Position Available: Senior Manager of Marketing The Senior Manager of Marketing will be the second member of the marketing team and will be jointly responsible for all marketing activities in support of upcoming international (outside the U.S.) launch of the TOGA TM System. The TOGA System will be the first procedure to market for endoluminal (incision-less, through the mouth) treatment of obesity, employing trusted technology (titanium staples) and proven mechanism of action (restrictive pouch). Potential market for this product is over $100 billion worldwide. Pilot published and unpublished data shows excellent weight loss results, and international product demonstrations have generated significant market excitement in advance of product launch. We are seeking a highly motivated candidate with interest in creating the business. This position reports to the Vice President of Marketing. Education: BA/BS, MBA a plus. Experience: 4-5+ years of medical device marketing experience, product launch experience, experience in obesity surgical devices a plus If interested, please submit your resume to hr@satietyinc.com.

9 Transcend Medical is the first portfolio company co-founded by ForSight Labs and The Foundry. Based in Menlo Park, Transcend is focused on the research and development of novel devices for the treatment of glaucoma, the leading cause of adult irreversible blindness. Over two million people in the US alone are afflicted with the disease today, and that number is expected to grow to three million by the year Transcend has focused its efforts on replacing the current treatment of glaucoma with a safer, more effective procedure with minimal complications. Join the Transcend team and be instrumental in the development of new devices and procedures that may prevent blindness. Transcend Medical offers competitive salaries, stock options, and the ability to participate during the early stage of the company s development with an enthusiastic and energetic team. Transcend Medical, Inc. is an Equal Opportunity Employer. For more information, please visit our website at Research & Development Engineers and Technicians: The ideal candidates will have five plus years of medical device experience developing Class III devices and successfully getting them through an approved PMA. Familiarity with all US and quality regulations related to manufacturing and development is required. Experience with the design and fabrication of small devices and components are a plus, including proficiency in SolidWorks. A bachelors or advanced degree in mechanical or chemical engineering is preferred. If interested, please submit your resume to hr@transcendmedical.com.

10 XTENT, Inc. develops customizable drug-eluting stent (DES) systems for the treatment of coronary artery disease. XTENT's customizable DES systems are designed to enable the treatment of single lesions, long lesions and multiple lesions of varying lengths and diameters, in one or more arteries with a single device. Founded in 2001, XTENT was incubated by The Foundry and incorporated in June XTENT has numerous US and international patents and patent applications covering a variety of delivery systems, stents, and coatings. The company currently has multiple studies underway to evaluate its Custom NX DES platform. XTENT, Inc. is an Equal Opportunity Employer. Positions Available: Analytical Chemist HPLC This position will be responsible for the chromatographic aspects of chemical analysis associated with combination medical devices, drug eluting stents (DES). The candidate will analyze chemical data, make project decisions; develop technical judgement by evaluating test results and suggest future product directions; document test data and chemical manufacturing or R & D processes; and draft technical reports and present results of work to small groups. Must have standard knowledge of basic chemical and engineering principles, theories, concepts, and utilize standard scientific and engineering practices and techniques. Principal R & D Stent Engineer Design and develop innovative medical devices in support of XTENT s strategic plan. This position will be the product expert and will lead the R & D team projects. Manager, Manufacturing Direct and coordinate activities of engineering departments to achieve timely goals. Develop and coordinate the design, manufacture, testing, and validation for new or existing products personally or through subordinates. Propose and execute broad Product, Process, and Cost Improvement Projects requiring participation from multiple departments within the organization. PLEASE APPLY ONLINE AT