CAREERS

Minerva Surgical recognizes the value and contributions of all our employees. We provide a challenging, rewarding, and exciting environment that will enable you to enhance your skills and make the most out of your career.

Our success depends upon recruiting and retaining talented, highly motivated, energetic people for a wide range of positions.

Minerva Surgical maintains a high-quality, team-oriented working environment with leadership that actively promotes diversity as a core value and top priority. We aim to attract, mentor, and retain the best talent from all backgrounds, and foster a culture in which all employees are empowered to achieve their maximum potential.

We invite you to explore our available opportunities to learn if there are positions open that match your skills, experience and interest.

CURRENT OPENINGS:-

SENIOR RESEARCH & DEVELOPMENT ENGINEER:

Responsible for mechanical engineering analysis of device components. Investigate and evaluate existing technologies. Research, develop, design, and evaluate mechanical and electro-mechanical materials, components, assemblies, processes, and equipment for our products and their components. Design and develop medical device components in full compliance with the company's design control requirements and consistent with FDA, ISO, and Medical Device Directives requirements. Ensure proper documentation consistent with the company's quality system. Plan R&D activities consistent with the company's quality policy and quality objectives. Develop new concepts from initial design to market release. Conduct feasibility studies to verify product and component capability and functionality. Coordinate project activities and support personnel. Maintain detailed documentation throughout all phases of research and development. Review or coordinate vendor activities to support our development processes. Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company's products. Provide mechanical engineering support in the resolution of product complaints and/or safety issues. Ensure lab notebooks are documented in a timely manner and consistent with the company's applicable standard operating procedure. Maintain good manufacturing practice (GMP) systems, including pre-production quality assurance procedures, pre-clinical testing programs, and post- production GMP compliance in coordination with the document control, clinical, and quality assurance functions.

JOB REQUIREMENTS:

Bachelor's degree in Mechanical Engineering or Biomedical Engineering and 6 years of progressively more responsible related work experience in the job offered, or as a Research Assistant. The 6 yrs. of experience must include 5 years of experience in: Class II & III medical device design and development; Design Verification Testing for PMA (Pre-Market Approval) products; Solidworks; MiniTab; JMP; Design and development of balloons for medical devices; GAGE Repeatability & Reproducibility design verification test methods.

WORK SCHEDULE:

40 hours/week; 9:00 a.m. to 5:00 p.m.

LOCATION:

Minerva Surgical Inc., 20195 Stevens Creek Blvd., Suite 120, Cupertino, CA 95014

Qualified applicants may contact Deborah Morgan at 408-252-0101 ext. 309, by Fax at 408-689-9616, or by eMail at Deborahm@hermesinnovations.com.
Please refer Job Code #: SRRDE2011