Production Associate

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 jnj.com.

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:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Assembly

Job Category:

Business Enablement/Support

All Job Posting Locations:

Irving, Texas, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re 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 https://www.jnj.com/medtech

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for Production Associate.

Purpose: Responsible for using equipment for the assembly and processing tasks to produce finished products according to established specifications. Accountable for adhering to all quality and safety guidelines.

 

You will be responsible for:

• Operates production equipment to produce subassemblies or finished products.

• Interprets instructions and specifications and uses to set up equipment.

• Checks products on assembly line to confirm that they are properly assembled and removes

defective products.

• Cleans and maintains equipment as needed.

• Assists with basic maintenance of tools or equipment and advises supervisor, shift/team leader

and area technician when tools or equipment need maintenance or repairs.

• Prepares accurate records/documentation related to quality and work in progress.

• Troubleshoots minor production problems.

• Identify, inspect and prepare for adequacy of use, the required-mandrels for

production.

• Prepare, monitor and test dispersion / materials for production.

• Dips mandrels in materials and remove shells from mandrels after processed.

• Interface/operate computer-controlled shell forming equipment used in the coating of mandrels

with dispersion.

• Remove shells from conveyor line, load and operate cure oven.

• Perform visual and thickness inspection of shells.

• Interface/operate MES computer system, interpret SPC data output and respond as

appropriate.

• Operates soak tanks and dryers.

• Perform equipment cleaning procedures as needed.

• Monitors and responds to equipment and process issues that may lead to non-compliance.

• Accountable for adhering to and enforcing all quality and safety guidelines.

• Identifies and elevates all immediate and potential quality, safety, or environmental issues

(material, procedure, and process) as observed.

• Inspects assemblies and sub-assemblies devices.

• Reviews device records, follow established procedures, and prepares necessary documentation as

required. Must maintain good manufacturing and documentation practices in accordance to procedures outlined according to cGMPs.

• Provide training to new employees or other team members as requested; in manufacturing processeswith the support of the Manufacturing Technical Lead or Department Lead Operator.

• Maintains an updated and current training record and adheres to training timelines.

• Participates in Safety initiatives and programs by either joining Environmental Health and

Safety (EHS) or reporting unsafe practices/conditions to shift/team leader.

• Identify continuous improvement opportunities for process and equipment. Helps to meet daily

efficiencies by focused approach to performing tasks compliantly and safely according to

procedure/process.

• Responsible for communicating business related issues or opportunities to next management

level

• Responsible for ensuring personal and Company compliance with all Federal, State, local and

Company regulations, policies, and procedures

• Demonstrate independent understanding and application of core GMP fundamentals, including but

not limited to: Data Integrity (DI), Good Manufacturing Practices (GMPs), and Good Documentation Practices (GDPs).

• Performs other duties assigned as needed

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.

#LI-Onsite 

 

 

Required Skills:

 

 

Preferred Skills:

GMP Auditing, GMP Compliance, GMP Environments, GMP Guidelines