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Manufacturing Engineer

ZenflowSouth San Francisco, California, United StatesOnsite

About Zenflow


Zenflow, Inc. is a privately held medical device company dedicated to improving treatment for patients suffering from urinary obstruction caused by enlarged prostate. The innovative Spring® technology was designed with the patient experience in mind and relies on a small spring-like coil that gently props open the urethra, restoring its normal function while preserving the natural anatomy. The Zenflow Spring System is an investigational device and is not approved for commercial sale.

POSITION OVERVIEW:


We are a dynamic medical device start-up seeking a Manufacturing Engineer to join our team. The ideal candidate will play an important role in scaling up clinical stage disposable medical devices in preparation for commercialization with primary focus on equipment and process development, cost, yield, assembly time improvement, and production support. 

MAJOR DUTIES AND RESPONSIBILITIES:


  • Design, implement, and improve manufacturing processes and systems, focusing on efficiency, cost-effectiveness, and quality, while ensuring compliance with safety and regulatory standards.
  • Partner with R&D in the design of implant delivery systems, CMOS based cystoscopes and implant retrieval device for improved manufacturability through part reduction, improved assembly techniques/fixturing in order to improve yields and labor content.
  • Train assemblers when transferring processes or products to production. 
  • Manage vendors and their schedules to obtain parts, assemblies, and equipment in a cost-effective and expedited manner.
  • Develop and conduct process validation testing protocols and document results. 
  • Ensure that processes/methods utilized are consistent with cost effective and reliable manufacturing practice. 
  • Identify and propose improvements to increase production throughput, minimize scrap, or improve quality of manufacturing process.
  • Work with R & D engineers and vendors to implement product and process changes that result in reduced labor content, increased process capability, and simplification of component fabrication and assembly methods.
  • Complete projects in a timely manner consistent with corporate objectives. 
  • Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company’s products. 
  • Provide support in the resolution of product complaints and/or safety issues. 
  • Support company goals and objectives, policies and procedures, and adherence to QSR and FDA guidelines.
  • Use Solidworks to create designs for manufacturing fixtures and equipment and to generate relevant engineering specifications.
  • Work from verbal, written or pictorial information to create designs and implement improvements for engineering staff.  

EDUCATION/EXPERIENCE REQUIREMENTS:


  • Bachelor’s degree in Mechanical Engineering or equivalent preferred.
  • Minimum of 3 years of related experience in the medical device industry.
  • Experience with injection molding, electronics component fabrication and assembly processes, welding, thermal and adhesive bonding processes, and additive and subtractive manufacturing methods for custom components. 
  • Experience with typical assembly methods for disposable medical devices. 
  • Experience scaling up products into Pilot or Production environments. 
  • Prefer advanced mechanical design experience and working knowledge of catheter assembly techniques/technologies.

  • Ability to work independently and balance multiple priorities in a fast-paced, FDA regulated environment.
  • Strong verbal and written communication skills.
  • Strong organizational and planning skills, with attention to detail.

This position is based in South San Francisco, CA. The expected salary range for this position is $95,000 - $115,000 plus equity and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training.

Life at Zenflow

Fourteen million men in the US and over 200 million worldwide suffer from urinary obstruction related to benign prostatic hyperplasia (BPH). The majority of men will experience symptoms of this disease at some point in life. BPH, also known as prostate enlargement, leads to urinary straining, frequency, urgency, and sleep disruption. Despite the high prevalence and significant quality of life burden of BPH, established treatments are limited to drugs, which have limited effectiveness, and surgery, which carries a high risk of sexual side effects. The Innoflow device uses a mechanism known to relieve BPH symptoms with a unique design that enables it to avoid the complications associated with prior solution attempts. Urologists can deploy the device in a simple, office-based procedure that is faster and more painless than any existing therapy.
Thrive Here & What We Value1. Patientcentric approach2. Continuous learning and innovation culture3. Quality system documentation and lab notebook keeping4. Crossfunctional collaboration and effective communication5. Regulatory compliance and adherence to FDA, ISO, and CE standards6. Innovative and patient-focused product development for urinary obstruction caused by enlarged prostate7. Spring technology designed with patient experience in mind
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