Job summary
Job post source
This job is directly from Penumbra, Inc.
Job overview
The Manufacturing Engineering Manager at Penumbra, Inc. leads engineering and manufacturing process development for medical devices, ensuring product quality and cost-effectiveness while managing a team and supporting cross-functional projects.
Responsibilities and impact
The role involves managing manufacturing engineering functions, leading product scale-up from R&D to production, ensuring compliance with quality systems, training staff, troubleshooting, and collaborating with product development teams to optimize manufacturability.
Compensation and benefits
The position offers a starting base salary range of $145,000 to $214,000 per year, with compensation varying by performance and skills, along with a comprehensive benefits package including medical, dental, vision, life insurance, 401(k) with employer match, employee stock purchase plan, paid parental leave, holidays, vacation, and sick leave.
Experience and skills
Candidates should have a bachelor's degree in engineering or related field with 5+ years of relevant experience, 1+ years of engineering management experience, medical device industry knowledge, familiarity with GMP and quality regulations, strong leadership and communication skills, and proficiency in Microsoft Office.
Career development
The company promotes a collaborative environment with continuous learning and performance rewards, offering opportunities to work on innovative medical therapies and grow professionally within a global healthcare company.
Work environment and culture
Penumbra fosters a collaborative teamwork culture focused on innovation, learning, and performance, with adherence to quality and compliance standards in a general office environment with some exposure to manufacturing settings.
Company information
Penumbra, Inc. is a global healthcare company headquartered in Alameda, California, specializing in innovative medical device therapies with a broad product portfolio addressing significant unmet medical needs worldwide.
Team overview
The candidate will manage a multidisciplinary project team within manufacturing engineering, overseeing staff development and cross-functional collaboration to achieve strategic goals.
Job location and travel
The position is located in Alameda, California, with minimal business travel (0-10%) and a general office environment with some physical activity and exposure to blood-borne pathogens.
Unique job features
This role uniquely combines leadership in manufacturing engineering with direct impact on medical device innovation and quality, offering involvement in cutting-edge product development and cross-functional team leadership within a regulated industry.
Company overview
Penumbra, Inc. is a global healthcare company that designs, develops, manufactures, and markets innovative medical devices and therapies. Specializing in neuro and vascular health, they generate revenue through the sale of products aimed at treating conditions such as stroke and peripheral artery disease. Founded in 2004, Penumbra has a history of pioneering advancements in minimally invasive medical technology, and they continue to expand their portfolio with a strong focus on research and development to improve patient outcomes.
How to land this job
Tailor your resume to highlight your experience in managing manufacturing engineering functions, especially within medical device development, emphasizing leadership in cross-functional teams and direct employee management.
Focus on demonstrating your expertise in GMP/Quality System Regulations, clean room practices, and your ability to lead quality system compliance and training initiatives.
Apply through multiple channels including Penumbra, Inc.'s corporate careers page and LinkedIn to maximize your visibility and application reach.
Connect with current employees in Penumbra's manufacturing engineering or medical device divisions on LinkedIn; ice breakers could include commenting on recent Penumbra innovations or asking about team culture and challenges in scaling new products from R&D to production.
Optimize your resume for ATS by incorporating keywords from the job description such as 'manufacturing engineering,' 'medical device,' 'GMP,' 'quality system,' 'cross-functional teams,' and 'design for manufacturability' to ensure it passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify relevant job boards, and discover LinkedIn connections, allowing you to focus your energy on preparing for interviews and networking effectively.
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