BU4 Shift Team Lead - B26

at  Johnson Johnson

Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson’s Family of Companies, is recruiting for a Band 26 - Business Unit 4 - Bioprocess Supply Manufacturing Team Lead
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.

ABOUT THE ROLE

We are currently seeking a highly motivated and experienced MSAT Engineer (Process Analytics) to join our Manufacturing Science and Technology (MSAT) team in Cork. As an MSAT Engineer (Process Analytics), you will play a key role in implementing and optimizing process analytics strategies to drive efficiency and reliability in our manufacturing processes.

RESPONSIBILITIES & THE IMPACT YOU WILL HAVE:

• Working assigned shift or day patterns to meet business needs and operations schedule.
• Coordination of operations team to meet production schedule in a safe, compliant and cost-effective manner.
• Completion of pulse walkdowns to ensure compliance with all regulatory requirements particularly in relation to the pharmaceutical industry, health and safety requirements and environmental legislation and cGMP requirements.
• Troubleshooting of process issues and escalating/collaborating with relevant support to resolve in a timely and effective manner.
• Review and approval of completed batch records.
• Support of Project and Commissioning/ Qualification activities as required