Quality Technician 1

Job description

Job Description

Requisition ID: 4409181012

DePuy Synthes part of the Johnson & Johnson Family of Companies is recruiting for a Quality Technician I located in Bridgewater, MA.

DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visitwww.depuysynthes.com .

Codman is a global neurosurgery business whose devices support hydrocephalus management, neuro intensive care and cranial surgery.

Johnson & Johnson has agreed to sell the Codman Neurosurgery (CNS) business to Integra LifeSciences subject to customary closing conditions and regulatory approvals. Please be advised that should you be hired, upon completion of this transition, your employment and the position with Codman Neurosurgery will transfer to Integra LifeSciences.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

The Quality Technician I will be responsible for ensuring company products comply with internal and external specifications by performing a variety of routine and non-routine inspections and evaluations. This includes activities related to Inspection and Testing, Batch Release and Records Management, First Article Inspection, and CMM.

You will:
• Perform routine product inspections and analyses, generally of finished goods, components, incoming materials, materials prior to be sent to external service suppliers, or new products, by observing, measuring and recording data. Utilization of blue print reading skills daily.
• Compare inspection results to defined requirements or specifications and documents differences found. Compile and input data into router, log book and/or computer databases and documents findings.
• Consult with more experienced personnel to confirm presence of non-conformances and subsequent product disposition.
• Provide external service suppliers with appropriate gages for calibration.
• Have general awareness of GD&T principles.
• Support broader quality efforts to assess impacted stock inventories (e.g. stock audits, stop shipments).
• Audit batch records to ensure compliance with policies, procedures and regulations.
• Ensure batch records are complete and accurate, with all NC's dispositioned prior to release.
• Identify, records and reports on batch non- conformances and product holds.
• Store and maintain batch files either physically or electronically based on established guidelines.
• Perform (moderately) complex tests and analyses to assure that products comply with established specifications.
• Carry out (difficult) calculations and prepares documentation that shows the results of tests performed.
• Operate automated equipment to inspect product per inspection program (e.g. CMM).
• Apply principles of Good Documentation Practices.
• Provide assistance in validation activities.
• Execute assigned NR actions within the applicable software application.
• Provide metrics and updates on executions.
• Maintain training records up-to-date.
• Perform document change management as per local procedures.
• Use of computer-based applications to manage inventories, batch records, down time, communication, inspection equipment, inventory equipment.
• Perform additional task on supervisor's request that are within experience and personnel capability.

Desired profile

Qualifications
• A minimum of a High School/Secondary Education or Equivalent is required.
• Basic computer skills including experience utilizing Microsoft Office is required.
• A Quality-oriented mindset is required.
• The ability to be flexible, service oriented, work in a team environment and collaborate is required.
• Excellent written, oral communication and organization skills are required.
• This position requires a daily commute to Bridgewater, MA for the 2nd shift working hours of 3:15pm – 11:45pm Monday - Friday with overtime and weekends as the business requires.

Primary Location
United States-Massachusetts-Bridgewater-
Organization
Depuy Orthopaedics. Inc. (6029)
Job Function
Quality Control
Requisition ID
4409181012