Demo

Quality Systems Analyst, Change Control

Johnson and Johnson
Plymouth, MA Full Time
POSTED ON 2/27/2025
AVAILABLE BEFORE 5/17/2025

Sterilmed Inc. is recruiting for a Quality Systems Analyst, Change Control, located in Plymouth MN, US. 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 / . For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges. We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential. At Johnson & Johnson, we all belong. As part of the Quality Systems team, we have responsibilities such as coordinating the change control documentation and approval process and provide quality support for technology transfer and improvement of existing processes. Conduct investigations, collection of data, analysis of trends, and preparation of reports for assigned quality processes. This role requires detailed understanding of regulations, process criteria, and business impact for decision-making and implementation of actions. You'll need to lead and support the current quality change control system and recommend improvements for the areas you will be supporting. We need your expertise and support to prepare for audits and inspections, and for the development, implementation, and review of standard operating procedures for interactions with internal and external customers. Key Responsibilities :

  • We need your help to monitor and track alignment to J&J Quality Standards and any other quality system initiatives.
  • Ensures quality systems are effectively deployed.
  • Responsible for Change Control activities as a Quality Systems SME.
  • Support and coordinate change control needs for the site.
  • Facilitate and guide change owners' activities.
  • Report metrics related to areas of support to appropriate review boards such as Management Review, Data review board, periodic metrics reporting, etc.
  • Responsible for communicating business-related issues or opportunities to the next management level. Education :
  • A Bachelor's or equivalent university degree in Science or Engineering field is required. Experience and Skills : Required :
  • 2-4 years of experience in Medical Device manufacturing or related proven experience.
  • Proven knowledge of quality system principles, practices, and processes such as Change Control, Change Design, and Data Analysis.
  • Prior experience in ISO 13485 and or QSR 820 FDA.
  • Ability to prioritize in a fast-paced environment
  • Excellent interpersonal relations and communication skills.
  • Skilled Microsoft (Excel, PowerPoint, SharePoint) knowledge. Preferred :
  • Knowledge of specific business software and software applications such as Windchill, EtQ, Compliance Wire, Minitab, etc. is preferable.
  • Ability to communicate effectively with a diverse collaborator.
  • Ability to work cooperatively with coworkers and complementary teams.
  • Strong oral and written communication skills abilities.
  • Skilled at preparing executive briefings and broad communications.
  • Ability to make confirmed decisions that will optimally support the business and company policies.
  • Multi-collaborative environment and rapid shift on assignments.
  • ASQ Certification(s) is preferable. Other :
  • Up to 10% of domestic travel is required. Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability. 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 .

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