Document Control Administrator

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: Quality Job Sub Function: Quality Control Job Category: Business Enablement/Support All Job Posting Locations: San Angelo, Texas, United States of America Job Description: Ethicon San Angelo is recruiting for a Document Control Administrator , located in San Angelo, TX. 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 The Document Control Administrator is responsible for making administrative decisions to meet departmental and internal customer needs. Responsible for ensuring documents submitted with changes conform to established standards. Also responsible for providing support to contributors to the change control process.

Performs as business system administrator for at least one of the electronic quality systems in the plant, e.g. ADAPTIV, LIMS, Compliance Wire, EtQ. Provides back up and support as business system administrator for at least two other electronic quality systems. Reviews quality aspects of change documents submitted for accuracy and consistency with other documents. Proofreads and edits documents for style, grammar, spelling, format, and impact it may have on other documentation. Provides assistance to change originators in change control processes and system tools. Generates reports and metrics on the change process as needed. Consults on document and data control business practices and helps reduce change cycle time. Conducts internal audits of the change management process. Supports process improvement and implementation. Analyzes processes and systems for alignment to business strategy. Verifies change implementation and approves closure of completed change orders. Performs as Site Record Coordinator; serves as liaison between department coordinators and Records Manager; performs internal records management compliance assessments as needed and implements / coordinates inactive storage solutions provided by external storage vendor. Demonstrates a thorough knowledge of facility and organizational policies and procedures. Provides presentations and education to all levels of the organization on regulatory, corporate, and local policies and procedures. Responsible for leading and participating in cross facility or plant teams as directed by Quality Systems Lead. Provides investigation, documentation, corrective action recommendations, and project management on assigned quality system improvements. Maintains necessary supplies and equipment. Provides periodic reports, completes special projects, and assists Quality Systems Lead as assigned – may act on behalf of the Quality Systems Lead to represent the site where Records Manager role is concerned. Performs a variety of other duties of a complexity commensurate with the job level as assigned or required. Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).