Finished Goods Release QA Coordinator

Johnson & Johnson

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profile Job Location:

Alameda County, CA - USA

profile Monthly Salary: Not Disclosed
Posted on: 15 hours ago
Vacancies: 1 Vacancy

Job Summary

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

San Lorenzo Puerto Rico United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at Surgery

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery Ready to join a team thats reimagining how we heal Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the worlds most prevalent conditions such as obesity cardiovascular disease and cancer. Patients are waiting.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for Finished Goods Release QA Coordinator.

Purpose: Under the direction of the Quality Manager or Quality Team Leader and with the objective of maintaining high-quality standards will coordinate the final product release process and maintain compliance with the regulatory requirements. Engaged in the Quality Assurance operation in accordance with the QSR ISO and Ethicon written inspection specification and quality standards. Analyses product related information to assure that products comply with established specifications. Prepare reports (using the computer system) as assigned. Completes record of inspection results acceptance rejection and disposition.

You will be responsible for:

  • Prepares documentation that shows the results of tests performed and prepare custom reports on results.
  • Review and complete transactions such as but not limited to batch records Sterilization Certificates of Processing and appropriate records retention in Manufacturing and Quality Systems to release Finished Goods products.
  • Advise about any non-conformance related to the QA inspection and test methodologies. Generate the Non-Conformance Report (NC) to the impacted Department.
  • Evaluate the precision and accuracy of products production equipment and/or testing equipment.
  • Use LIMS and JDE software to document the inspection results and disposition to product prior to release.
  • Collect or oversee the collection of Finished Goods and Retain samples at the sterilization site when needed for testing and for evaluation.
  • Performs data analysis and recommends disposition of material. Segregate Finished Goods samples and Retain Samples according to the requirements.
  • Generate Certificate of Analysis (COA) as per Clients and other Plants Requests.
  • Support Sterilization Diversion activities.
  • Work with two different Sterilization Suppliers and assists as required.

Qualifications / Requirements:

  • An Associate Degree (in a science or technical field is preferred) with a minimum of four (4) years of experience within Quality Assurance Department is required; or Bachelors degree in science with four (4) years professional experience is required.
  • 10% travel requirement between Ethicon Locations Domestic and/or international travel is required.
  • Availability to work overtime various work schedules which may include 1st 2nd 3rd shifts and/or 12-hour daily shifts including weekends and holidays is required.

Johnson & Johnson is an 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 disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

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Required Skills:

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Required Experience:

IC

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
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  • Corporate Communications
  • Apache Commons
  • Compensation
  • Civil Quality Control

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About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more

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