Pre-Production Operator I (R&D)

Join VitalPath in New Hope as a Pre-Production Operator I!

About VitalPath
VitalPath is a trusted contract manufacturing partner that delivers high-quality complex catheter solutions around the world that save lives and restore patient health and vital function. We strive to treat every product we design and manufacture to the highest level of quality and awareness that these products are going to be used inside of a patient, possibly even our own family members.

Our employees impassioned hard work and dedication are at the core of our success. Every function within our organization plays a crucial role in our mission and is deeply valued for its contribution to achieving our shared goals of quality, innovation, continuous improvement, and operational excellence.

As a fast-growing organization, we bring harmony and standardization across VitalPath with a strong vision in mind - We are one VitalPath. We embrace our diversity, celebrate each others success, support one another through change, and continue to grow as a high-performing organization. We aim to shape our corporate culture to enhance team member engagement, skills, and productivity so that VitalPath is an employer of choice. If you’re ready to contribute to groundbreaking medical advancements in a collaborative, fast paced environment, we invite you to apply and be part of our growth!

About the Position
The Pre-Production Operator I is responsible for performing a variety of highly complex catheter assembly tasks. This position is expected to work on challenging projects with minimal or no supervision and be able to effectively communicate with all members of the Research & Development team. This position is expected to complete tasks accurately according to specifications and within defined timelines to support Research & Development Projects.

Shift/Schedule

• Monday - Friday 6am-2:30pm

• Read, understand and follow Standard Operating Procedures, Work Instructions, manufacturing processes per as defined on travelers, Good Documentation Practices (GDP), current Good Manufacturing Practices and safety procedures
• Understand proper lot traceability for materials and products
• Responsible for completion of manufacturing documentation completely, correctly and in a timely manner
• Explain problems, provide feedback to others and receive feedback effectively
• Maintain VitalPath’s quality and workmanship standards in all aspects of the job and complete inspection of product against these standards
• Execute assembly of complex catheters according to documentation/prints in order to meet required deadlines
• Manage working on multiple builds within a single shift
• Complete material returns, including executing material counts and updating label, upon completion of builds
• Assist in documenting and monitoring personal performance
• Maintain a clean general work area during shift, including performing line clearance as needed
• Use proper inspection tools to complete visual and dimensional inspection of product; Identify and communicate instances of non-conforming product
• Identify challenges and issues and communicate them effectively and in a timely manner to responsible R&D Line Lead, Technician and/or Engineer.
• Take initiative to find work when necessary

• High School diploma, GED or equivalent
• Ability to follow written and verbal instructions
• Experience working in medical device assembly in a controlled environment
• Attention to detail
• Proficient in reading, writing, and speaking English
• Ability to read and understand basic measurements
• Understanding of basic math skills
• Working understanding of processes used in catheter assembly including, but not limited to, liner stretching, coiling and braiding, reflow/thermal bonding processes, skiving heat shrink, annealing and cutting braid, terminating braid and coils, and loading extrusions
• Working understanding of dimensional inspection and visual workmanship requirements
• Willing to work in a team environment and promote collaboration across functions
• Ability to perform job with limited supervision
• Must be able to lift 25lbs
• Must be able to sit/stand for an extended period of time in a cleanroom environment
• Must be able to work under a microscope for extended periods of time

• 1-3 years experience working in Research & Development OR 3-5 years experience working in production assemble

• Comprehensive, Low Cost Health and Dental Insurance Plans Available
• Vision Insurance
• Health Savings Account with company contribution
• Short and Long Term Disability
• Supplemental insurances (short term disability, AD&D, life insurance, and more)
• Paid Time Off
• Sick Time Off
• Paid Holidays
• 401K with company match
• Competitive compensation
• Opportunities for career growth and advancement

VitalPath is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, work related mental or physical disability, veteran status, sexual orientation, gender identity, or genetic information. VitalPath participates in E-Verify.