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Senior Scientist Proteins AD - Container Closure Integrity

jj · Schaffhausen

Nouveau
Senior 🇬🇧 English
Container closure integrity testing Residual seal force testing Head space analysis Helium leak detection GMP Regulatory documentation Scientific writing

Description du poste

About the role

The Container Closure Integrity (CCI) team is a development laboratory within the global Research & Development organization, operating in the GMP environment of Johnson & Johnson Innovative Medicine Supply Chain. It supports biologics and advanced therapy products (antibodies, cell and gene therapies, antibody-drug conjugates) across oncology, immunology and neuroscience. The company is looking for a Senior Scientist to lead projects for early- and late-phase development programs and commercial products, helping to expand laboratory capabilities and deliver compliant analytical strategies and procedures.

Key responsibilities

  • Lead project coordination, development and validation of CCIT, SBIT and related assays for container closure systems and devices used in cell and gene therapy, antibody and antibody-drug conjugate programs.
  • Coordinate method development, validation and transfer in line with internal guidance and health authority expectations.
  • Provide timely scientific support for investigations and other high-priority requests with short turnaround times.
  • Align project plans, deliverables, timelines and risks with internal and external partners, and represent the team in project meetings as a subject matter expert.
  • Write technical documents such as study and validation protocols and reports, and compile, interpret and communicate analytical data.
  • Propose process improvements and evaluate emerging technologies to build fit-for-purpose laboratory capabilities.

Required profile

  • Master's degree with at least five years of relevant experience, or PhD with at least two years, in life sciences, materials science, analytical or pharmaceutical development.
  • Experience with container closure systems (vials, prefilled syringes, cartridges, bags, needle-based or on-body delivery devices) is advantageous.
  • Experience in a pharmaceutical or other GMP-regulated environment is preferred.
  • Excellent written and spoken English; German is desirable.

Required skills

  • Analytical development, GMP compliance and regulatory documentation
  • Container closure integrity testing (CCIT), residual seal force testing, head space analysis and helium leak detection
  • Scientific writing, project coordination and investigation support

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Source : ats:workday

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jj

Schaffhausen