LifeCycle Management Specialist (Primary Packaging)

LifeCycle Management Specialist (Primary Packaging)

• Location: 100% Remote

• Duration: Dec 31, 2026

• Hours: 40

Imagine your next project ensuring the highest quality standards for medicines reaching patients worldwide.

Patients inform and inspire our science-based innovations, which continue to change and save lives. The ideas and research of our people translate into medications that advance patient care.

roles and responsibilities.

You will be the central point of contact for lifecycle activities, specifically managing change controls related to Supplier Change Notifications.

This will involve:

• Leading and fully managing all change controls associated with Supplier Change Notifications for primary packaging materials within the portfolio.

• Managing the end-to-end process from initiation to closure, acting as the bridge between external vendors and internal technical teams.

• Writing comprehensive Comparability Reports to assess the processability of materials.

• Drafting and reviewing Material Qualification Reports.

• Creating, managing, and reviewing test protocols and final reports.

• Reviewing and evaluating technical specifications from suppliers to ensure strict alignment with internal quality standards.

• Coordinating all functional technical testing required, ensuring internal functional teams execute necessary tests to validate vendor changes.

• Coordinating complex timelines and deliverables between vendors and internal labs across global networks (US, Belgium, Switzerland, South Korea).

how to succeed.

To be successful in this role, you will need a strong eye for compliance, quality assurance, and data accuracy, combined with the ability to manage stakeholders effectively in a remote environment.

You will also bring:

• A Bachelor’s degree in Engineering (Packaging, Materials, Mechanical, or Chemical), Pharmaceutical Sciences, or a related scientific discipline (Master’s preferred).

• Strong technical knowledge of Primary Packaging Materials.

• Minimum 3-5 years of relevant professional experience in Life Cycle Management (LCM)Understanding of Drug Product (DP) Filling Lines.

• Proven experience managing Change Controls and Supplier Change Notifications.

• Proficiency in Comet, SAP, and Minitab

• Advanced proficiency in Microsoft Excel & PowerPoint.

• Excellent communication skills for remote collaboration.

benefits.

This role offers a very competitive hourly rate. This contract will run until Dec 31, 2026.

you are welcome here.

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. The ideas and research of our people translate into medications that advance patient care.

application process.

We are looking to process the first round of applications within the next 2 working days. We do not accept applications via email.

Diversity, Equity & Inclusion.

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.