Danaher Corporation Quality Technician II in Lodi, California
Quality Technician II is the interface for assuring product quality during the manufacture of injection molded consumables in the use of Cepheid/Danaher Life Science Diagnostics finished goods with the support of Quality Engineering, Manufacturing Engineering, and Consumables Engineering. In this position, the Quality Tech II supports the company’s’ efforts for confirming that the acceptance criteria and appropriate quality standards were sustained through the production cycle per the required product specifications. Quality Technician II support operations on the floor, support quality decision making and is required to engage in Quality, Compliance, Safety and Continuous Improvement Initiatives.
Quality Technician II is responsible for allocating resource and training for junior team members daily on the manufacturing floor. Quality Technician II are to act proactively to ensure smooth team operations and effective collaboration. Lead by setting a good example and engage the team to achieve goals. Quality Technician II work closely with Lead and Supervisors.
Quality Technician II are responsible for the accuracy of measurements, reporting or escalating as applicable, documenting when appropriate, and adhering to pertinent regulations and policies.
This position utilizes a variety of manual, automatic, and semi-automatic machines in order to inspect and verify part conformity.
ESSENTIAL JOB RESPONSIBILITIES:
Create an inspiring team environment with an open communication culture
Coordinate and manage rework
Coordinate and manage NC rework task
Sustain and ensure Compliance
Attend daily management meeting
Understand customer impact
Oversee day-to-day operation
Participate in cross function project
Discover training needs, documentation revision updates and provide coaching
Recognize high performance and reward accomplishments
Encourage creativity and risk-taking
Responsible to produce injection molded consumables within the Lodi facility-controlled environments.
Adherence to applicable health, safety procedures and will be required to wear appropriate Personal Protective Equipment.
Maintains cleanroom standards, practices, and housekeeping according to Standard Operating Procedures such as Daily PM, conveyor and runner clean up.
Quality resource for all issues pertaining to the quality of the product from incoming inspection to the final inspection release of the consumable product. Makes day-to-day decisions on product quality
Conducts required testing, inspection, and review of procedures during the manufacturing process to ensure that products comply with quality standards.
Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance or adherence to conformity or applicable standards.
Utilizing applicable diagnostic equipment or tests to collect, analyze, and record findings in order to determine conformity when appropriate, including failure investigation, consumable alert or advanced trouble shooting.
Lead through DBS, use PSP for problem solving
Responsible for confirming Batch Records, Production logs completeness and compliance with QSR requirements.
Responsible for the final release of production goods and to analyze, review accuracy of data in order to certify or reject material.
Performs 2nd review/release approval of lots.
Responsible for applying statistical quality control procedures where required.
Escalate through the initiation of a Nonconformance Report (NCR) when nonconformity is found per applicable procedures within a timely and accurate manner.
Provide communication or updates to management.
Perform advanced visual inspection, dimensional measurement, and functional testing as required.
Identify and support requalification activities with manufacturing engineering
Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability
Performs advanced inspection with specialized equipment including the following Micro-Vu, Keyence Optical Measurement Systems, and product specific functional tests
Audits documentation and production floor to verify conformity to quality and compliance standards
Performs and participates in layered audits, internal audits, vendor audits as necessary
Provides training related to the quality processes used in the manufacturing process
Participate in continuous quality improvement projects and other related activities as assigned.
Collaborates with cross-functional team to complete projects or tasks, including justifying immediate manufacturing matters or interests.
Perform other duties as required or requested.
Education or Experience (in years):
Minimum requirements by meeting one of the following:
High School diploma (or equivalent experience) with 4-5 years of related work experience working in plastic injection molding and 3 + years in working in a Quality position.
Bachelor’s degree in related field with 1-2 years of experience
Knowledge and skills:
Experience in compiling data to support metrics analyzing current process.
Knowledgeable in Advanced Microsoft Office software.
Ability to interface effectively with a cross-functional team environment.
Strong attention to details skills.
Posture and Movement equal to but not less than requirement of the following:
Other: Technical Qualification
Capable of measurement conversion(s).
Ability to interpret engineering drawings, schematic diagrams, formulas, and visual aids in the disposition of material conformity.
Capable of consulting with management or engineering staff to determine and maintain quality and reliability standards.
Detailed and quality oriented.
Must be knowledgeable of definitions of critical, major, and minor characteristics.
Understand the x, y, and z coordinate system.
Demonstrates consistent quality, traceability, and controls standards.
Capable of using inspection planning tools.
Determine sample size for lots.
Understand and demonstrate random sampling or testing methodology.
Identify and report non-conforming material.
Knowledge of Standard Operating Procedures (SOPs) and Quality assurance terminology.
Use Ishikawa diagrams, 5 Whys, or other root cause analysis techniques.
Creation of flow charts, check sheets, and control charts.
Understand cost of quality and Plan-do-check-act quality cycle.
Basic knowledge of Six Sigma or Continuous Improvement Lean.
Statistical techniques, production processes, Acceptable Quality Level (AQL), trend charts.
Plot data and recognize out-of-control conditions.
Identify/recognize inspection errors and initiate resolution that includes documenting/recording.
Understand basic processing and the relation to defects.
Must have basic inspection techniques.
Basic calibration knowledge.
Measure using surface plate layouts.
Intermediate knowledge and experience with SAP/MES ERP.
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at 202.419.7762 or email@example.com to request accommodation.If you’ve ever wondered what’s within you, there’s no better time to find out.
Operating Company: Cepheid