Process Scientist

il y a 1 semaine


Antwerpen, Flandre, Belgique Johnson & Johnson Temps plein

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.


We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.
**J&J Innovative Medicines is recruiting a Process Scientist.


MSAT Small Molecule Drug Product is accountable for capturing and intensifying the scientific cornerstones and leading productivity, compliance, and sustainability throughout the commercial lifecycle.


Responsibilities:

  • Act as process SME supporting multidisciplinary product teams at latestage drug product development, technical transfer, PPQ and commercial manufacturing operations by means of
- sensitivity analysis and process capability analysis.
- root cause analysis for quality, stability, and yield deviations.

  • Responsible for experimental design, coordination and/or execution of lab
- and pilot-scale unit operations, modelling, and statistical analysis, writing/reviewing/approving of protocols, reports and regulatory submissions.

  • Support initiatives for process robustness optimization and competitiveness.
  • Leverage networking and influencing skills to ensure good collaboration with partners in MSAT, TDS, PES, Quality, Regulatory, MAM and DOTS.

Qualifications:

Requirements:

  • Advanced degree in Pharmaceutics, Biotechnology, Engineering, Physics, or related area
years of experience in development of solid dosage formulations or unit operation modeling with experimental proficiency in compression and coating processes

  • Strong knowledge of solid dosage manufacturing processes (batch, continuous), process control, and quality assurance.
  • Experienced with unit operation scaledown model development, characterization, and scaleup
  • Preferably first experience with modeling software for process simulation and optimization,
  • Experience with statistical packages for experimental design and analysis or PATmodel development.
  • Excellent analytical and problemsolving skills, with the ability to interpret data, identify trends, and draw actionable insights.
  • Effective interpersonal and communication skills, with the ability to articulate technical concepts to diverse audiences and collaborate effectively with crossfunctional teams.
  • Language: English
  • Ability to think critically and creatively and pay attention to detail.
  • Experience with problemsolving and risk analysis methodologies.
  • Good presentation and technical writing skills.
  • Knowledge of regulatory requirements and guidelines related to pharmaceutical manufacturing (e.g., FDA, EMA) is preferred.

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