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**Job Function: **
Supply Chain Engineering
**Job Sub Function: **
Packaging Design Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
**About Innovative Medicine **
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Senior Principal Engineer, Primary Container, Biologics in Malvern, PA.
Purpose: The Senior Principal Engineer Primary Container, Biologics, will lead the development, selection, qualification, and lifecycle management of vial systems, pre-filled syringes, cartridges, and emerging container technologies for new biologic drug products. The role ensures all primary containers comply with global regulatory, technical, and quality standards while driving innovation and operational excellence. It is part of the global Drug Delivery Systems (DDS) Team. The position reports to the Global Head Drug Delivery Systems, Malvern, PA (US).
You will be responsible for:
Strategic Leadership & Governance
Define and implement the global strategy for primary containers supporting biologics across the JJIM portfolio.
Oversee development, qualification, and lifecycle management of vial systems, pre-filled syringes, cartridges, and new container technologies.
Ensure compliance with global regulatory requirements and internal quality standards.
Partner with cross-functional teams (R&D, Quality, Regulatory, Supply Chain) to align container solutions with product needs.
Lead risk assessments and mitigation strategies for container systems.
Manage vendor relationships and evaluate new technologies to enhance performance and patient safety.
Provide technical leadership and subject matter expertise for regulatory submissions and inspections.
Drive innovation and the implementation of new technologies across biologics packaging.
Drive continuous improvement and innovation in container technologies.
Manage a technical team to deliver a portfolio of projects.
Technical Expertise & Development
Oversee the design, evaluation, and qualification of primary container systems including vials, pre-filled syringes, cartridges, stoppers, and seals.
Provide scientific leadership on container–closure integrity (CCI), extractables and leachables (E&L), materials compatibility, and device-drug interface requirements.
Ensure container strategies support formulation stability, manufacturability, and patient usability.
Project & Portfolio Management
Partner across CMC, Formulation, Device Engineering, Quality, and Manufacturing to drive product development programs.
Manage timelines, resources, and budgets for container-related activities.
Lead risk assessments, mitigation strategies, and governance reviews.
Manage a technical team, delegate tasks and escalate challenges in a timely manner.
Regulatory & Compliance
Ensure compliance with global regulatory expectations (FDA, EMA, ICH, ISO, USP/EP/JP).
Author and review regulatory documentation for IND, IMPD, BLA, and NDA submissions.
Serve as SME during regulatory inspections and health authority interactions.
Qualifications/Requirements:
**Education: **Minimum of a Bachelor's Degree in in Pharmaceutics, Material Science, Biomedical Engineering, Chemical Engineering, or a related field is required.
Skills/Experience:
- Minimum of 10 years of experience in biologics drug product development, packaging science, or container–closure engineering is required.
- Proven leadership experience in pharmaceutical or biotech environments is required.
- Demonstrated experience with pharmaceutics and regulatory submissions is required.
Technical Skills
- Expertise in CCI testing, extractables/leachables, materials compatibility, and aseptic processing is preferred.
- Strong understanding of combination product regulations and CMC expectations is required.
- Specific expertise in pre-filled syringe systems is preferred.
Leadership & Soft Skills
- Strong leadership, team-building, and cross-functional collaboration skills.
- Excellent communication and strategic problem‑solving abilities.
- Ability to manage complex portfolios with multiple competing priorities.
Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.
**Required Skills: **
Preferred Skills:
Coaching, Competitive Landscape Analysis, Engineering, Good Manufacturing Practices (GMP), Lean Supply Chain Management, Package and Labeling Regulations, Package Management, Process Improvements, Product Packaging Design, Science, Technology, Engineering, and Math (STEM) Application, Standard Operating Procedure (SOP), Sustainability, Sustainable Packaging, Tactical Planning, Technical Credibility, Transparency Reporting, Validation and Qualification Policies, Procedures and Programs