.Johnson & Johnson Innovative Medicine are recruiting for a Director MSAT LM Cross Platform Engineering to be based in Schaffhausen, Switzerland or Leiden, The Netherlands or Beerse, Belgium.At Johnson & Johnson, we believe health is everything.Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.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.As a Director MSAT LM Cross Platform Engineering, you will hold a strategic role within Global MSAT and will partner with R&D, Make functions, New Product Introduction, the Quality Organization and Value Chain Management teams, as well as internal manufacturing sites and external partners, such as contract manufacturing organizations, to develop and implement robust manufacturing processes.Key Responsibilities:Responsible for strategic framework around LM DP parenteral products in conjunction with other key disciplines to develop and deploy a JJIM enterprise methodology on a Gravel-to-Grave process on robust aseptic manufacturing.Single Point of Contact (SPOC) for MSAT needs for LM and parenteral products with regard to aseptic manufacturing processes, sterilization technologies, visual inspection, validation and continued process verification.Manage communities of practices and know-how around critical sterile manufacturing practices like sterilization technologies, aseptic manufacturing, visual inspection and life cycle process validation (CPV) within the firm.Proactively promote quality and compliance in the areas of sterile manufacturing and validation and coach others to do the same.Manage a highly engaged MSAT team providing strategic leadership and direction aligned with the global LM network.Oversee technical support to regulatory filings, regulatory inspections, and health authority questions.Collaboration in technology transfer projects supporting implementation of new processes in manufacturing operations.Lead and supervise a team of engineers and scientists. Coach, develop and guide team towards company, platform and team goals & objectives.Qualifications:Strong expertise in pharmaceutical manufacturing processes, with a focus on low bio-burden and sterile manufacturing
