Document Control Administrator

Johnson & Johnson • San Angelo, TX

1d • Onsite

About The Position

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.

Requirements

• Associate or equivalent level degree required
• 6-8 years of related experience
• Demonstrated competency in the ETHICON network office application software or ability to quickly achieve competency
• Software expertise in multiple software applications as well as PC hardware knowledge.
• Team skills including problem solving, conflict management, communications skills – both verbal and written, analytical and systems thinking, and strong organizational skills.

Nice To Haves

• Windchill, EtQ and Quin experience.

Responsibilities

• 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).
• 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.

Benefits

• This position may require up to 5% travel, both domestic and international.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree