Johnson & Johnson

Senior Engineer, Primary Container, Biologics

Johnson & Johnson$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Packaging Engineering, Material Science, Biomedical Engineering, Chemical Engineering, or related field; Advanced degree preferred.
  • 5+ years in biologics drug product development, packaging science, or container-closure engineering.
  • Proven leadership in pharmaceutical or biotech environments.
  • Experience with commercial biologics and regulatory submissions.
  • Expertise in CCI testing, extractables/leachables, and materials compatibility.

Responsibilities

  • Execute global strategy for primary containers in biologics.
  • Oversee development and lifecycle management of various container systems.
  • Ensure compliance with global regulatory and internal quality standards.
  • Collaborate with cross-functional teams to align packaging solutions with product needs.
  • Lead risk assessments and vendor management for container technologies.
  • Provide technical leadership for regulatory submissions and inspections.
  • Drive innovation in biologics packaging and continuous improvement efforts.

Benefits

  • Flexible work environment with hybrid options.
  • Opportunity for professional development and growth.
  • Contribution to impactful projects in drug delivery systems.
  • Engagement in innovative packaging technologies.
Full Job Description

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:

We are searching for the best talent for Senior Engineer, Primary Container, Biologics in Malvern, PA.

Purpose: The Senior Engineer Primary Container, Biologics, will lead the development, selection, qualification, and lifecycle management of vial systems, pre-filled syringes, cartridges, cell therapy bags 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.

You will be responsible for:

Strategic Leadership & Governance

  • Execute 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.

Technical Expertise & Development

  • Support the development of advanced therapy packaging including cell therapy bags and cryo-capable container closure systems.
  • 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.

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 Packaging Engineering, Material Science, Biomedical Engineering, Chemical Engineering, or a related field is required. Advanced degree is required.

Experience/Skills:

  • Minimum of 5 years of experience in biologics drug product development, packaging science, or container–closure engineering.
  • Proven leadership experience in pharmaceutical or biotech environments.
  • Demonstrated experience with commercial biologics and regulatory submissions.

Technical Skills

  • Expertise in CCI testing, extractables/leachables, materials compatibility, and aseptic processing.
  • Strong understanding of combination product regulations and CMC expectations.
  • 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.

#LI-Hybrid

 

Required Skills:

 

 

Preferred Skills:

Coaching, Critical Thinking, Detail-Oriented, EHS Compliance, Engineering, Good Manufacturing Practices (GMP), Lean Supply Chain Management, Package and Labeling Regulations, Package Management, Process Improvements, Product Packaging Design, Quality Assurance (QA), Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Sustainability, Sustainable Packaging, Technologically Savvy, Validation Testing

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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