This job posting is anticipated to close on Jun 16 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.
Description
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As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
QualityJob Sub Function:
Quality ControlJob Category:
ProfessionalAll Job Posting Locations:
San Lorenzo, Puerto Rico, United States of AmericaJob Description:
Job Summary
MedTech Surgery Puerto Rico s recruiting for a QA Data Specialist, located in San Lorenzo, Puerto Rico. This role will report to Quality Team Leader, Quality Operations Leader, Quality Operations Lead or designee and with the objective of maintaining high quality standards for the product manufacturing process and the compliance with the regulatory requirements. Supports and maintain quality data in our system, performs data analysis and performs other functions to support the Quality Assurance Department at Ethicon LLC. Engage in the Quality Assurance operation in accordance with the QSR, ISO and Ethicon written specifications and quality standards. Main point of contact and Subject Matter Expert for the Site’s Inventory Control System (ERP System, i.e. SAP) from a Quality Assurance perspective. Works closely with the ERP users, including key business functions to ensure up to date and accurate data in our ERP systems.
Key Responsibilities:
Under the direction of Quality Team Leader, Quality Operations Leader, Quality Operations Lead or designee and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
- Manage QA Data within ERP System. Transactions performed by this resource will be the following (but additional transactions may be performed):
- Manage transactional Issues to move/transfer material to inventory.
- Perform corrections or changes in manufacturing and/or expiration date of Finished Goods Lots and/or raw materials, in accordance with procedures.
- Perform corrections to Finished Goods lots including reclassification, batch status changes, among others.
- Inspection Lot issues/Cancellation of Inspection Lots.
- Manage Subcon Report Issues.
- Execute Wind-shuttle templates, conducting SWFT Tickets, and execution of task as Ethicon QA Data Departmental Lead (DDL).
- Create tickets for Adding/Removing Accesses to ERP system.
- Conduct training to new users in the ERP process and/or procedures.
- Execute validations for ERP process enhancement.
2. Execute material hold control process in ERP systems required.
3. Submit changes and support implementation of changes in the documentation system.
4. Support the effective implementation of programs that help improve the overall quality of product and process within area of responsibility.
5. Support internal and external audits.
6. Maintain knowledge of all procedures, changes to specifications and new regulations related to the area of responsibility.
7. Maintain control of nonconforming raw materials, following applicable procedures.
8. Support Plant operations in solving quality data issues affecting the supply chain process.
9. Keep records of all performed tests following GDP and GMP procedures.
10. Perform other duties as required by department leaders as needed.
11. Responsible for communicating business related issues or opportunities to next management level.
12. Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
13. Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
Qualifications
Education:
Associate Degree with 4 years of experience within the Quality Department in regulated industry or Bachelor’s Degree (Science or Technical Field preferred) with 2 or more years of experience within Regulated Industry.
Experience and Skills:
Required:
- Knowledge in ERP systems for quality data process
- Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts
- and/or 12-hour daily shifts, including weekends and holidays.
- Intermediate or higher computer skills and use of software application(s).
- Bilingual (Spanish & English)
- Excellent organizational, time management and interpersonal and follow up skills.
- Able to communicate effectively with multiple levels of the organization.
- Knowledge of QSR and ISO Standards.
Preferred:
- Knowledge in SAP system transactions and functionality.
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.]
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 & 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, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
