Juno Pacific
  • 03-Nov-2017 to 02-Jan-2018 (EST)
  • JunoPacific, Soquel
  • Soquel, CA, USA
  • Salary
  • Full Time

JunoPacific combines the full resources of facilities located in key medical device markets in Minneapolis/St. Paul and the Silicon Valley, focusing on medical molding and assembly. Services range from tooling, part design and prototyping to micro/close tolerance molding, single and true multi-shot injection molding, vertical molding, reel-to-reel, insert molding, complex tooling that includes Spin-stack and rotary platen, multi-component/multi-material product assembly, secondary operations and validated sterile packaging.


Position Summary

Reports directly to the Manufacturing Manager. Facilitates the daily activities related to the manufacture of components and/or finished product in the Department. Provides leadership and motivation to technical and hourly associates to achieve desired quality, quantity, service and cost standards through safe and proper utilization of materials and equipment.


Essential Job Functions

  • Provides Leadership in a facilitator roll to assigned technical and hourly associates to achieve departmental quality, quantity, service, cost and safety goals. Facilitates team meetings as required and participate in associate projects as a team member.
  • Assures compliance to appropriate regulatory requirements. Initiates corrective activities when not in compliance and informs department Manufacturing Manager of noncompliance and proposed corrective activities.
  • Instructs and facilitates training of associates in the performance of their job in a safe and efficient manner, following prescribed procedures as detailed in the job description, specifications, policies, and hazardous materials communication requirements.
  • Recommends and/or initiates personnel activities such as selection, transfer, discharge, disciplinary actions and associates complaints in a fair, consistent and timely fashion so as to comply with company Human Resources policies.
  • Recommends, initiates, or facilitates measures from associates to improve production methods, equipment performance, product quality, changes in working condition and use of equipment so as to increase efficiency, improve quality and reduce waste.
  • Coordinates daily /weekly production schedules with CER Clerk, Inventory Clerk Team, and Leads to assure timely issuance of work orders and materials necessary to maximize operating efficiencies and service levels. Analyzes work order variances. Coordinates with Inventory Team corrective activities to resolve material variances.
  • Coordinates the department preventative maintenance program to assure equipment is properly maintained to minimize downtime and meet FDA, EPA, and OSHA requirements.
  • Issues request and monitors completion of all service and repair work to be performed necessary to maintain safe, clean and efficient operation.
  • Maintains a working set of specifications and other documents required to support the manufacture of components and finished goods under plant and FDA quality regulations. Maintains appropriate manufacturing documentation.
  • Initiates and maintains accurate records and reports of daily production and waste, batch component and process inspection data sheets, inventory documents, Staffing Agency Timecards, Production Work Order charges, associate status changes, levels of absence, disciplinary warnings and any other records necessary for the satisfactory performance of the operation.
  • May lead, guide, and train employees, interns, and/or volunteers performing related work; may participate in the recruitment of volunteers, as appropriate to the area of operation.
  • Maintains Class 7 Cleanroom good housekeeping and organization at all times.
  • Performs miscellaneous job-related duties as assigned.


Minimum Experience & Education

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


  • Required a BS or BA degree in technical or business related field and minimum of 2 years supervisory experience, preferably Injection Molding operations in a Clean Environment.
  • Must have demonstrated leadership abilities; excellent organizational & critical thinking skills; high sense of urgency; strongly motivated; balanced perspective; and an effective communicator at all levels.
  • Previous high speed manufacturing experience in a technical or lead role highly desirable.
  • Experience in medical device assembly, and experience with Lean Manufacturing and ERP highly desirable.
  • Must display a hands-on assembly, understand Test Equipment functionality, understand and trouble shoot ultrasonic welding and all other CR Equipment.
  • Some Experience with ERP System (IQMS/BAAN).
  • Experience MS Excel and MS Word for charts and reports.
  • Considerable physical activity. May require handling of objects that can weigh up to 40 lbs.
  • Requires being 90% present inside the Cleanroom to support Assembly Operation.
  • Work is normally performed in a Class 7 Cleanroom Environment.

 Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law.



Juno Pacific
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