QUALITY CLERK (TEMPORARY 12 MONTHS)

At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com/.

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

We are searching for the best talent for QUALITY CLERK (TEMPORARY 12 MONTHS) to be in Juarez, Chih., in Plant Independencia.

Purpose:

• Quality Assurance Clerk Supports all activities related to the Quality System, being reflected in the Quality Systems Metrics.
• Verifies purchase orders requisitions to be in compliance with approved suppliers list. (Main Activity/ handling of documents in English)

You will be responsible for:

• Educate, train, and provide support consultation with defect tracking system or complaint/product evaluation management system (Siebel).
• Help maintain a document retention system for the Juarez facility.
• Support records management archiving and controlling documents, such as DHR scanning, record archival, etc.
• Maintain accurate and precise documentation of their daily and weekly activity sheets.
• Oversees the product evaluations and NCR/CAPA assignments made by WWQC to the Juarez sites:
• Support NC/CAPA site leader preparing track and trending information, as required.
• Generates reports —as required- for product evaluation status to site management.
• Supports NC/CAPA site leader and/or Product Quality Leader providing awareness to manufacturing line associates on findings from products evaluations.
• Support training for new users on ETQ System for NC/CAPA process as required.
• Requests quotations to suppliers and generate purchase orders as required
• Assists in the implementation of company systems improvements as required.
• Provide support during External and Internal Audits (e.g.: document retrieval, consultation, etc.)
• Maintain knowledge of all procedures, change to specification and new regulations related to their areas of responsibilities.
• Participates in safety initiatives within the facility.
• Be aware of and comply with Company’s safety policies.
• Ensure proper safety and environmental procedures and practices are utilized.
• Participates on departmental and company continuous improvement activities
• Create and send COA’s by request.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed