Quality Assurance (Qa) Specialist

Robotics & Digital Solutions, part of the Johnson & Johnson family of companies, is recruiting for a Quality Assurance (QA) Specialist position located in Santa Clara, CA.

Robotics & Digital Solutions is part of Ethicon, Inc., a global leader in surgery with products and solutions found in almost every operating room around the world. Ethicon has made significant contributions to surgery for more than 100 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including robotics, digital solutions, sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com

General Summary

Ensures company products follow internal and external specifications by performing a variety of routine and non-routine inspections and evaluations.

Key Duties & Responsibilities

• Confers with other departments regarding quality standards
• Request minor adjustments to documentation, accepts/rejects items, or reroutes for rework based on established guidelines and knowledge of production techniques
• Provide training and support to quality assurance team members that covers systems, policies, procedures, and core processes
• Recommends adjustments to production process to correct standard problems
• Identifies workmanship defects and recommends corrective action
• Drive continuous improvement of core processes to ensure manufacturing quality assurance is maintained while efficiency is optimized
• Participates in the establishment of future inspection procedures
• Compiles and inputs data, documents findings and interprets results
• Train and aid less experienced members of the QA team on quality procedures, protocols, and documentation
• Review of cGMP and other GxP documents to ensure company processes comply
• Maintain quality assurance documentation
• Reports rework/reject to proper department. Follows up on corrective actions being taken
• Train production staff on quality procedures, protocols, and documentation
• Compiles and maintains quality requirements documentation
• Investigates production process to determine root cause
• Ensures proper documentation and disposition of defective products
• Performs varied documentation/product inspections by observing, measuring, and recording data. Compares inspection results to defined requirements or specifications and documents differences found

Additional Responsibilities

• Good decision-making skills
• Excellent oral communication skills
• Use applicable software systems as needed for the job (i.e., SAP, Agile, MES/SQL, etc.)
• Accurately complete records as defined within the job procedures (i.e., manual and/or electronic documentation)
• Follow Quality Management System requirements as defined within procedures and instructions

Key Individual Contributor Competencies

• Listens effectively and remains open to other’s ideas
• Build strong productive relationships
• Demonstrates the courage to stand alone on ideas and opinions that differ from others
• Effectively manages and adapts to change
• Holds oneself accountable for compliant and detailed execution
• Seeks opportunities to gain experience and develop professionally
• Uses best practices to improve QA department operations
• Excellent verbal and written communication skills
• Demonstrates ability to collaborate with teams and individuals
• Vocational, Certificate, Technical or Associates required
• Attention to detail and strong administrative skills
• Collaborates effectively with people that have diverse styles, talents, and ideas
• Maintains the highest standards of ethical behavior
• Asserts personal ideas and opinions using persuasion to influence others

Experience

Required:

• Requires 6-8 Years of related work experience

Other

• Daily start time is between 6:00 am & 7:00 am
• No “Remote Work” available for this position
• 100% of the Work is on-site in support of Manufacturing

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.

For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com.

Primary Location

NA-US-California-Santa Clara

Organization

Auris Health, Inc. (6267)

Relocation Eligible

No

Travel

No

Job Function

Quality Control

Job Qualifications

Education: