Verification & Validation Manager

B. Braun Group

$110K — $140K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8-10 years in medical device development or 5-7 years with a Master's degree in science/engineering related to medical devices.
  • 2+ years of experience supervising technical staff.
  • Experience in regulated environments is a plus.
  • Familiarity with IEC standards relevant to medical device development.
  • Hands-on experience with standard test equipment and troubleshooting electronics.

Responsibilities

  • Direct and manage the Verification and Validation (V&V) engineering group.
  • Create and maintain test cases, protocols, and reports for product compliance.
  • Oversee execution of hardware and system testing against product requirements.
  • Ensure compliance with FDA and EU guidelines in V&V practices.
  • Develop test automation frameworks to enhance defect detection.
  • Collaborate with project managers for timely project completion.
  • Provide technical support for customer inquiries and reported issues.

Benefits

  • Onsite working model fostering collaboration and teamwork.
  • Structured workweek from Monday to Friday.
  • Focus on management and leadership roles, enhancing career growth opportunities.
Full Job Description
Digital Surgery Systems Inc.

Job Posting Location: Goleta, California, United States

Functional Area: Research and Development

Working Model: Onsite

Days of Work: Wednesday, Tuesday, Thursday, Friday, Monday

Shift: 5X8

Relocation Available: No

Requisition ID: 10614

SUMMARY

This position will direct and oversee the teams, processes, and tools responsible for product verification and software validation testing, including software quality assurance. It is responsible for the creation and maintenance of test cases and protocols to ensure that product and software quality standards are achieved, and that all regulatory expectations are met. It will also oversee the execution and reporting of Verification test efforts, including document approval and release. This role will interface closely with software engineering, systems engineering, biomedical/clinical engineering, product management, project management, quality, and regulatory.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

  • Develop, lead, and manage the V&V engineering group.
  • Define and track goal progress for individual team members
  • Support the development and maintenance of Product and Software Requirements Specifications
  • Develop test cases, protocols, and plans; Perform and oversee execution of these test cases, protocols, and plans; Deliver final test reports
    • Hardware and system testing against the product requirements, including testing against optical standards, visual perception and mechanical capability
    • Preparation for and Management of External Testing, including: Safety testing per IEC-60601-1, Wireless, Shipping, EMC Testing, etc.
    • Understand accelerated lifecycle testing to prove reliability
    • Software verification testing against the software requirements specifications.
  • Introduce V&V best practices in compliance with FDA and EU medical device product development, and measure team performance against best practices
  • Develop test automation framework to achieve (1) early defect detection and (2) reduced manual test effort.
  • Manage hardware and software resources required to support testing
  • Work with project managers to ensure that projects are completed on time, and within budget.
  • Contribute as needed to help the V&V team to achieve project goals and milestones
  • Act as the technical point-of-contact for customer reports issues and provide support to the Technical Support team as needed.


COMPETENCIES To perform the job successfully, an individual should demonstrate the following competencies:
  • Ability to manage V&V team members
  • Understanding of medical device product regulations, FDA and EU
  • Ability to maintain high team morale through excellent communication, management, and encouragement.
  • Demonstrated ability to creatively and proactively solve problems.
  • Flexible in working under changing and different work settings.
  • Demonstrate knowledge of the company product development lifecycle and the process tools.


QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education/Experience

Mandatory
  • Requires a minimum 8-10 years' experience in medical device development with a bachelor's degree or 5-7 years' experience in medical device development with a Master's Degree in science/engineering from an accredited university, or equivalent work experience in medical device development.
  • Minimum of 2 years' experience supervising technical staff.


Desirable
  • Experience developing medical devices, or working in a regulated environment
  • Understanding of IEC-60601-1, IEC-14971, and IEC-62304 for medical device development
  • Experience being in the operating room (OR) supporting live surgeries as a design engineer, tech. support, service engineer, or sales representative. Knowing OR sterility protocols, medical equipment
  • Understanding basic image processing concepts and techniques
  • Hands-on background in operation and use of standard test equipment; oscilloscopes, digital multimeters, frequency generators, calipers etc. Ability to troubleshoot and analyze electronics.
  • Background in software test automation
  • Knowledge of different medical imaging modes such as optical microscopy, intraoperative fluorescence, X-rays, CT scans, MRI, OCT, etc.
  • Experience working with Scrum/Agile


Language

Demonstrate excellent communication and documentation skills, both written and oral. Ability to read, analyze, and interpret technical procedures or governmental regulations. Ability to write reports and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.

Math

Demonstrate ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Apply concepts of basic algebra and geometry.

Reasoning

Demonstrate ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

Computer Skills

To perform this job successfully, an individual should have strong computer skills, knowledge of Microsoft Word, Excel and Outlook. The individual should also be able to troubleshoot PC-based systems, hardware, and software.

PHYSICAL REQUIREMENTS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this Job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee must frequently lift and/or move up to 30 pounds and occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include color, distance and close vision.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is frequently exposed to work near moving mechanical parts. The noise level in the work environment is usually moderate.

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