Manager, GD Quality Management (Open)

Location: Horsham, Pennsylvania, United States of America, or Titusville, New Jersey, United States of America

Salary: $117,000–$201,250 per year

Company

Johnson & Johnson MedTech develops healthcare and medical technology solutions as part of Johnson & Johnson's broader healthcare innovation business.

What you will do

• Lead process, training, and personnel qualification projects, including process mapping and training development and delivery.
• Partner with Global Development, business stakeholders, quality groups, and governance teams to maintain an effective GxP Quality Framework.
• Manage project tasks, timelines, deliverables, risks, issues, and progress reporting.
• Support the digital transformation roadmap toward data-centric content and qualification management systems.
• Support or lead additional projects, meetings, audits, and inspections.

Requirements

• Bachelor’s degree in Science or Business; a master’s degree is preferred.
• At least five years of experience in a medium- to large-scale matrix organization, including at least five years in pharmaceutical or device compliance.
• Exceptional written and oral English communication skills are required.
• Knowledge of global clinical and preclinical safety and pharmacovigilance regulations and life sciences regulatory frameworks.
• Experience managing complex projects, analyzing business processes, and implementing improvements.
• Ability to build cross-functional relationships, work autonomously, and foster an inclusive environment.

Nice to have

• Experience in process design and training design.
• Master’s degree in Science or Business.
• Knowledge of business process management, ISO 9001, quality validation, SOPs, and process governance.

Culture & Benefits

• Full-time professional role within the R&D Quality organization.
• Collaborative work across business partners, quality groups, governance teams, and diverse departments.
• Focus on inclusive collaboration, diversity, and respect for individual contributions.
• Opportunity to contribute to digital transformation in pharmaceutical and device quality operations.