Senior Scientist, Sterile Drug Packaging & Development

GlaxoSmithKline

Upper Providence (Delaware County)

On-site

USD 90,000 - 130,000

Full time

14 days+
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Job summary

GlaxoSmithKline is seeking a Formulation Product Development professional to provide packaging support from prototype evaluation to commercial launch. You will work with DDS, Clinical and Global Supply Chain teams to define packaging strategies and ensure regulatory alignment for packaging components.

The role emphasizes development of sterile packaging, design control, and validation testing, with responsibilities spanning material assessments, cross-functional collaboration, and risk

Qualifications

  • BS/MS/PhD with a strong foundation in packaging science or equivalent.
  • Experience interpreting regulatory standards for packaging.
  • 3+ years developing and implementing packaging solutions.

Responsibilities

  • Lead packaging development activities to support qualification, registration, and launch milestones.
  • Assess materials and technologies for technical performance and cost.
  • Author container closure sections and design control documentation for IND/NDA CTX/MAA.
  • Support project strategies for packaging across multiple functions and partners.
  • Ensure compliance with global standards and packaging validation activities.
  • Manage external partnerships and technology transfer efforts.
  • Characterise container closure systems for compatibility with drug products.

Skills

Pharmaceutical Formulations
Product Management
Product Design
Quality by Design
Regulatory Filings
Stability Testing
Technology Transfer
Drug Delivery
Molecular Modeling
Product Planning
Product Strategies
External Manufacturing
Pharmacokinetics

Education

Bachelor's degree in Engineering or related scientific discipline
Master's degree in Engineering or related scientific discipline
PhD in Engineering or related field

Job description

GlaxoSmithKline is seeking a Formulation Product Development professional to provide packaging support from prototype evaluation to commercial launch. You will work with DDS, Clinical and Global Supply Chain teams to define packaging strategies and ensure regulatory alignment for packaging components.

The role emphasizes development of sterile packaging, design control, and validation testing, with responsibilities spanning material assessments, cross-functional collaboration, and risk

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