This job posting is anticipated to close on Jun 05 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.
Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain ManufacturingJob Sub Function:
Manufacturing AssemblyJob Category:
Business Enablement/SupportAll Job Posting Locations:
Santa Clara, California, United States of AmericaJob Description:
Johnson & Johnson is hiring for a Lead Operator - Shockwave Medical to join our team located in Santa Clara, CA.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Production Lead is responsible for assembly, testing, and inspection of product according to documented Manufacturing Process Instructions (MPIs), including cleaning and setup of workstation with proper equipment and materials. Supports Production Supervisors to coordinate schedules and workload to meet production requirements. Records functions and activities performed on Lot History Records (LHRs) and other Quality Records. Leads the efforts of their assembly team to comply with the company’s policies and procedures, including quality, safety, environmental, and business practices. The Production Lead is considered the Subject Matter Expert (SME) on all stations of the assigned product line.
Essential Job Functions
Reviews LHR to ensure correct documentation is at workstation(s); obtains new documentation (i.e., latest MI revision) from supervisor or lead, if necessary.
Setup equipment obtains tools and materials required by LHR.
Cleans workstations/equipment and performs line clearance per documented procedures.
Signs/dates documentation to verify completion of setup procedures.
Builds subassemblies and/or final assemblies per MPIs.
Performs in‑process inspections (i.e., qualitative [visual or tactile] and quantitative [dimensional]) of components/materials, subassemblies, and final assemblies to ensure that specifications are met and/or for data collection and analysis (e.g., statistical process control [SPC]).
Monitors equipment parameters and results of in‑process inspection(s); as necessary, adjusts according to documented procedures to ensure product meets appropriate quality specifications.
Prepares labeling, audits labeled product for product information per LHRs (e.g., part number, description, expiration date), and assembles final product packaging. Records and dispositions labeling materials used, destroyed, and leftover from packaging operations.
Ensures that only products labeled correctly are released to finished goods according to documentation.
Records details of work and completes required portions of LHR to ensure traceability of each finished product lot. Assists supervisor with inventory control issues (e.g., scrap transactions, back flushing of finished products and subassemblies). Completes LHRs for review.
Records process and product measurement data for quality control purposes, as required.
Documents scrap resulting from out-of-specification equipment, materials, processes (i.e., non-conforming materials) according to documented procedures and notifies supervisor that disposition and/or corrective action may be required.
Initiate non-conformance reports (NCRs) as needed.
Contributes to experimental builds using documented guidelines provided by engineers to assist in the product development process.
Records results using data collection forms provided by engineers.
Contributes to the development of improved manufacturing methods by sharing ideas with engineers and management through both verbal and written communication.
Champions and leads 5S and Lean Manufacturing initiatives.
Schedules workforce and workload accordingly to meet production requirements.
Trains SMEs based on industry standards.
Supports new operators’ development and current operators’ providing continuous feedback on performance.
Enforces CER codes of conduct, policies and procedures.
Trains and is certified to all stations of 2 product lines.
Other duties as assigned. These job requirements are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel.
Provides instructions to direct employees’ efforts. Implements and adjusts schedules based on business needs to prevent line down situations.
Requirements
High school diploma or equivalent experience.
Must be able to read and communicate in English.
At least five (5) years of experience in assembly of medical devices.
Requires minimal supervision for routine work and close supervision for special assignments.
Ability to assemble, and test medical devices, including soldering, gluing, and assembly under the microscope while following Manufacturing Process Instructions (MPI), Standard Operating Procedures (SOP), Work Instructions (WI), etc.
Previous experience with QAD, preferable.
Capable of filling out detailed LHRs while following Good Documentation Practices (GDP).
Ability to work in a fast-paced environment while managing multiple priorities.
Operate as a team and/or independently while demonstrating flexibility to changing requirements.
There may be continuous sitting for prolonged periods and may be required to lift objects up to 15 pounds.
Additional Information
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
Required Skills:
Preferred Skills:
Agile Manufacturing, Assembly Operations, Communication, Data Savvy, Execution Focus, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Science and Technology (MSAT), Plant Operations, Predictive Analytics, Predictive Maintenance, Problem Solving, Process Oriented, Quality Auditing, Repair Management, Safety-Oriented, Technologically SavvyThe anticipated base pay range for this position is :
$69,000.00 - $111,090.00Additional Description for Pay Transparency:
