Operations Readiness Lead
Listed on 2026-09-16
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
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 Med Tech, 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 As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Supply Chain Engineering Job Sub Function:
Facilities Engineering Job Category:
People Leader All Job Posting Locations:
Wilson, North Carolina, United States of America
Job Description
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at Learn more and apply to this exciting new role for a Green Field Project!
Key Responsibilities- Leading the design and set‑up of manufacturing operations for parenteral drug products to ensure products are produced in compliance with cGMP, ISO, and other Regulatory requirements.
- Supporting the design of the manufacturing processes and areas in the construction of the new facility.
- Ensuring that operations activities are planned and performed to meet business needs, customer needs and production schedule.
- Promoting a culture of continuous improvement and open communication.
- Using performance management, people development, talent planning and other processes to lead, empower and develop individuals within operations.
- Shaping the site outcomes and new organization design as part of the Project Leadership team.
- Lead and sponsor multi‑functional teams to support site objectives.
- Providing strategic/operational leadership to the capital project.
- Lead by example and always strive to perform in compliance with Credo and Global Leadership Profile.
- Responsible for ensuring the safety of our operations employees and for following good environmental practices and procedures.
- Demonstrate safe behavior in every activity.
- Provide support to Project Commissioning, Qualification and Validation activities and actively support the Technology Transfer process for each new product.
Bachelor’s degree in engineering, Science, or equivalent technical field is required; MS or equivalent experience preferred.
Experience and Skills- Required: Minimum of 12 years of experience within pharmaceutical or GMP regulated operations environment with specific knowledge of parenteral drug product manufacturing.
- Proven capability of leading and implementing transformational change, as well as being able to effectively communicate and influence at all levels of the organization.
- Proven experience in managing partnerships and cross‑functional teams.
- Good problem‑solving skills.
- Experience managing diverse, multi‑disciplinary teams with varying degrees of educational background.
- Excellent interpersonal skills, ability to lead a team and operate as a part of team.
- Track record of building strong teams, attracting, and developing outstanding talent, motivating them through challenging circumstances and provide guidance & coaching as needed.
- Experience working…
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