Drug Product Process Engineer, Continuous Manufacturing & Data

Johnson & Johnson is currently recruiting for a Drug Product Process Engineer, Continuous Manufacturing & Data located in Titusville, NJ; Geel, BE; or Beerse, BE!

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. Learn more at https://www.jnj.com/.

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.

We are seeking a highly skilled and experienced Drug Product Process Engineer with expertise in continuous manufacturing, data analytics, and regulatory compliance to join our innovative team. As the Drug Product Process Engineer, you will be responsible for developing, optimizing, and ensuring the compliance of drug product manufacturing processes using continuous manufacturing techniques and for the deployment of innovation at our drug product manufacturing sites. Your knowledge of continuous manufacturing principles, data analysis, and regulatory requirements will be essential in improving process efficiency, product quality, and compliance.

Responsibilities:

• Develop and optimize drug product manufacturing processes using continuous manufacturing principles, ensuring robust and efficient operations.
• Utilize advanced data analytics techniques to monitor, analyze, and improve process performance and product quality in real-time.
• Collaborate with cross-functional teams including Research and Development, Formulation, and Quality Control to develop and implement continuous manufacturing and innovation strategies.
• Conduct data-driven process investigations and root cause analysis to identify and troubleshoot process deviations and quality issues.
• Design and execute experiments to evaluate critical process parameters and develop control strategies for drug product manufacturing.
• Stay updated on the latest regulatory requirements and guidance related to continuous manufacturing and drug product process development.
• Collaborate with equipment vendors and external partners to evaluate and select suitable continuous manufacturing technologies and equipment.
• Provide technical support and training to manufacturing personnel on continuous manufacturing processes and data analytics.
• Foster a culture of continuous improvement within the organization through data-driven decision making and process optimization.