Manager, GD Quality Management (Open)
J&J Family of Companies · Hopewell, NJ
FULL-TIME
Posted Oct 1, 2026
Job Description
Manager, Process & Personnel Qualification Management Expert
Join Johnson & Johnson's R&D Quality Team!
Are you eager to learn, collaborate, and make a positive impact? As a Manager in Process & Personnel Qualification Management, you will drive compliance and quality excellence in the pharmaceutical industry. In this role, you will lead process improvement projects and use the latest digital tools to support the transformation from traditional processes and training into a data centric content and qualification management system.
What You'll Do:
You will lead process and training related projects, including process development, mapping, and training development/qualification and delivery.
You will be a vital quality partner for Global Development, promoting collaboration and serving as a link between business partners, quality groups, and governance. This role ensures that our GxP Quality Framework effectively adapts to both business and regulatory changes in a proactive manner.
Your ability to manage tasks, timelines, and deliverables will be crucial for achieving successful project outcomes. Additionally, you will address issues, managing risks, and providing timely updates to management and business owners regarding project progress.
You will support the implementation of our digital transformation roadmap, driving our evolution towards data-centric content and a robust qualification management system.
Qualifications and Required Knowledge:
Education: At a minimum a Bachelor's degree in Science or Business is required (Masters degree is preferred).
Experience: A minimum of 5 years in a medium to large-scale matrix organization, with at least 5 years focused on pharmaceutical/device compliance. Preferred experience includes process design and training design.
Communication Skills: Exceptional proficiency in both oral and written English communication, with a talent for articulating complex ideas in a clear and effective manner.
Regulatory Knowledge: Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations and guidelines, coupled with experience in the life sciences industry's regulatory framework.
Project Management Skills: Demonstrated expertise in managing intricate projects and fostering collaboration among diverse teams and departments.
Analytical Skills: Keen attention to detail and robust analytical thinking abilities to evaluate business processes and implement improvements.
Leadership and Networking: Established track record in personal leadership, building relationships, working autonomously, and cultivating an inclusive work atmosphere that values diversity.
Required Skills: Business Process Management (BPM), Business Requirements Analysis, Coaching, Compliance Management, Cross-Functional Collaboration, Data Savvy, Fact-Based Decision Making, ISO 9001, Leverages Information, Process Governance, Process Improvements, Process Optimization, Quality Control (QC), Quality Standards, Quality Validation, Stakeholder Engagement, Standard Operating Procedure (SOP), Tactical Thinking, Technical Credibility
The anticipated base pay range for this position is: $117,000.00 - $201,250.00
Join Johnson & Johnson's R&D Quality Team!
Are you eager to learn, collaborate, and make a positive impact? As a Manager in Process & Personnel Qualification Management, you will drive compliance and quality excellence in the pharmaceutical industry. In this role, you will lead process improvement projects and use the latest digital tools to support the transformation from traditional processes and training into a data centric content and qualification management system.
What You'll Do:
You will lead process and training related projects, including process development, mapping, and training development/qualification and delivery.
You will be a vital quality partner for Global Development, promoting collaboration and serving as a link between business partners, quality groups, and governance. This role ensures that our GxP Quality Framework effectively adapts to both business and regulatory changes in a proactive manner.
Your ability to manage tasks, timelines, and deliverables will be crucial for achieving successful project outcomes. Additionally, you will address issues, managing risks, and providing timely updates to management and business owners regarding project progress.
You will support the implementation of our digital transformation roadmap, driving our evolution towards data-centric content and a robust qualification management system.
Qualifications and Required Knowledge:
Education: At a minimum a Bachelor's degree in Science or Business is required (Masters degree is preferred).
Experience: A minimum of 5 years in a medium to large-scale matrix organization, with at least 5 years focused on pharmaceutical/device compliance. Preferred experience includes process design and training design.
Communication Skills: Exceptional proficiency in both oral and written English communication, with a talent for articulating complex ideas in a clear and effective manner.
Regulatory Knowledge: Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations and guidelines, coupled with experience in the life sciences industry's regulatory framework.
Project Management Skills: Demonstrated expertise in managing intricate projects and fostering collaboration among diverse teams and departments.
Analytical Skills: Keen attention to detail and robust analytical thinking abilities to evaluate business processes and implement improvements.
Leadership and Networking: Established track record in personal leadership, building relationships, working autonomously, and cultivating an inclusive work atmosphere that values diversity.
Required Skills: Business Process Management (BPM), Business Requirements Analysis, Coaching, Compliance Management, Cross-Functional Collaboration, Data Savvy, Fact-Based Decision Making, ISO 9001, Leverages Information, Process Governance, Process Improvements, Process Optimization, Quality Control (QC), Quality Standards, Quality Validation, Stakeholder Engagement, Standard Operating Procedure (SOP), Tactical Thinking, Technical Credibility
The anticipated base pay range for this position is: $117,000.00 - $201,250.00
Additional Details
- City
- Hopewell
- State
- New Jersey
- Country
- US
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