General Summary
Join us as a leader in engineering, design, and development of innovative medical devices. In this role, you will manage the successful transfer and scale-up of products from R&D to Production while ensuring high standards of quality and cost-effectiveness. Additionally, you will make critical decisions regarding project plans and resource allocation.
What You'll Work On
- Lead the manufacturing engineering activities for development projects within a multidisciplinary team.
 - Oversee the creation, implementation, and maintenance of manufacturing processes and equipment to enhance efficiency and product quality.
 - Navigate and guide teams through our Quality System and compliance requirements.
 - Recruit, train, and develop your team, providing clear objectives and regular performance feedback.
 - Facilitate cross-functional team collaboration in line with our strategic direction.
 - Provide engineering support to operations and mentor junior engineers.
 - Work independently to execute engineering tasks and propose innovative solutions.
 - Collaborate with product development teams to ensure designs are manufacturable.
 - Create detailed production drawings and documentation.
 - Document engineering processes using protocols and reports to ensure thorough understanding and compliance.
 - Identify and collaborate with vendors to optimize process development.
 - Research and integrate new technologies to enhance product and process capabilities.
 - Train engineers and production staff on new techniques and methods.
 - Analyze issues to determine root causes and implement corrective actions.
 - Communicate and document test findings and recommendations effectively.
 - Review and update product design specifications to meet project needs.
 - Comply with the Company's Quality Management System (QMS) and relevant regulations.
 
What You'll Bring
Bachelor's degree in engineering or a related technical field with at least 5 years of experience; a Master's degree is preferred.Minimum of 1 year of experience in engineering management.Proven experience in the medical device industry.Strong understanding of GMP, Quality System Regulations, and clean room practices.Exceptional knowledge of engineering principles and the ability to lead and motivate teams.Excellent communication skills, capable of coaching and supervising team members.Proficiency in Microsoft Office applications.Working Conditions
The role is based in a general office environment in Alameda, CA, with a business travel requirement of 0% - 10%. There is potential exposure to blood-borne pathogens, and the position requires lifting up to 25 pounds. Activities involve standing, walking, sitting, and using a computer for extended periods.
Location and Pay
Alameda, CA
Starting Base Salary : $145,000 / year - $214,000 / year. Compensation may vary based on performance and experience.
What We Offer
We provide a collaborative environment where learning and performance are valued. You will have the opportunity to effect real change in the field of medical devices and enjoy a comprehensive benefits package including medical, dental, vision, life insurance, retirement plans, and paid time off.
Penumbra, Inc. is a global leader in healthcare innovation, with a strong commitment to addressing significant medical challenges. We prioritize equal opportunity in our hiring process.