Quality Assurance (QA) Specialist in Santa Clara, CA
Quality Assurance (QA) Specialist - Johnson & Johnson - Santa Clara, CA - work from home job
Company: Johnson & Johnson
Job description: 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:
• Performs varied documentation/product inspections by observing, measuring, and recording data. Compares inspection results to defined requirements or specifications and documents differences found
• Request minor adjustments to documentation, accepts/rejects items, or reroutes for rework based on established guidelines and knowledge of production techniques
• Recommends adjustments to production process to correct standard problems
• Compiles and inputs data, documents findings and interprets results
• Reports rework/reject to proper department. Follows up on corrective actions being taken
• Confers with other departments regarding quality standards
• Compiles and maintains quality requirements documentation
• Participates in the establishment of future inspection procedures
• Identifies workmanship defects and recommends corrective action
• Investigates production process to determine root cause
• Ensures proper documentation and disposition of defective products
• Drive continuous improvement of core processes to ensure manufacturing quality assurance is maintained while efficiency is optimized
• Maintain quality assurance documentation
• Provide training and support to quality assurance team members that covers systems, policies, procedures, and core processes
• Train and aid less experienced members of the QA team on quality procedures, protocols, and documentation
• Train production staff on quality procedures, protocols, and documentation
• Review of cGMP and other GxP documents to ensure company processes comply
Additional Responsibilities:
• Follow Quality Management System requirements as defined within procedures and instructions
• Use applicable software systems as needed for the job (i.e., SAP, Agile, MES/SQL, etc.)
• Excellent oral communication skills
• Good decision-making skills
• Accurately complete records as defined within the job procedures (i.e., manual and/or electronic documentation)
Key individual contributor competencies:
• Excellent verbal and written communication skills
• Build strong productive relationships
• Demonstrates ability to collaborate with teams and individuals
• Asserts personal ideas and opinions using persuasion to influence others
• Seeks opportunities to gain experience and develop professionally
• Uses best practices to improve QA department operations
• Holds oneself accountable for compliant and detailed execution
• Effectively manages and adapts to change
• Demonstrates the courage to stand alone on ideas and opinions that differ from others
• Listens effectively and remains open to other's ideas
• Collaborates effectively with people that have diverse styles, talents, and ideas
• Maintains the highest standards of ethical behavior
• Attention to detail and strong administrative skills Education:
• Vocational, Certificate, Technical or Associates required
Experience
Required:
• Requires 6-8 Years of related work experience
Other:
• 100% of the Work is on-site in support of Manufacturing
• No "Remote Work" available for this position
• Daily start time is between 6:00 am & 7:00 am
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.
Expected salary:
Location: Santa Clara, CA
Job date: Wed, 20 Sep 2023 22:16:56 GMT
Apply for the job now!
Apply Now
Apply Now
Company: Johnson & Johnson
Job description: 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:
• Performs varied documentation/product inspections by observing, measuring, and recording data. Compares inspection results to defined requirements or specifications and documents differences found
• Request minor adjustments to documentation, accepts/rejects items, or reroutes for rework based on established guidelines and knowledge of production techniques
• Recommends adjustments to production process to correct standard problems
• Compiles and inputs data, documents findings and interprets results
• Reports rework/reject to proper department. Follows up on corrective actions being taken
• Confers with other departments regarding quality standards
• Compiles and maintains quality requirements documentation
• Participates in the establishment of future inspection procedures
• Identifies workmanship defects and recommends corrective action
• Investigates production process to determine root cause
• Ensures proper documentation and disposition of defective products
• Drive continuous improvement of core processes to ensure manufacturing quality assurance is maintained while efficiency is optimized
• Maintain quality assurance documentation
• Provide training and support to quality assurance team members that covers systems, policies, procedures, and core processes
• Train and aid less experienced members of the QA team on quality procedures, protocols, and documentation
• Train production staff on quality procedures, protocols, and documentation
• Review of cGMP and other GxP documents to ensure company processes comply
Additional Responsibilities:
• Follow Quality Management System requirements as defined within procedures and instructions
• Use applicable software systems as needed for the job (i.e., SAP, Agile, MES/SQL, etc.)
• Excellent oral communication skills
• Good decision-making skills
• Accurately complete records as defined within the job procedures (i.e., manual and/or electronic documentation)
Key individual contributor competencies:
• Excellent verbal and written communication skills
• Build strong productive relationships
• Demonstrates ability to collaborate with teams and individuals
• Asserts personal ideas and opinions using persuasion to influence others
• Seeks opportunities to gain experience and develop professionally
• Uses best practices to improve QA department operations
• Holds oneself accountable for compliant and detailed execution
• Effectively manages and adapts to change
• Demonstrates the courage to stand alone on ideas and opinions that differ from others
• Listens effectively and remains open to other's ideas
• Collaborates effectively with people that have diverse styles, talents, and ideas
• Maintains the highest standards of ethical behavior
• Attention to detail and strong administrative skills Education:
• Vocational, Certificate, Technical or Associates required
Experience
Required:
• Requires 6-8 Years of related work experience
Other:
• 100% of the Work is on-site in support of Manufacturing
• No "Remote Work" available for this position
• Daily start time is between 6:00 am & 7:00 am
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.
Expected salary:
Location: Santa Clara, CA
Job date: Wed, 20 Sep 2023 22:16:56 GMT
Apply for the job now!
Apply Now
Apply Now