Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Filling Equipment

Johnson & Johnson•Wilson, NC

2d•Onsite

About The Position

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 jnj.com . 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. As a part of the Global Process Engineering team, the Sr. Princ. Process Eng – DP Aseptic Biotherapeutic Filling Equipment will serve as a recognized technical leader and SME, playing a pivotal role in shaping the future of aseptic drug product manufacturing. This role owns end‑to‑end process engineering leadership for the design, implementation, and start‑up of state‑of‑the‑art aseptic filling line systems (vial and syringe) within a new cGMP manufacturing facility. Using deep scientific, engineering, and business expertise, this leader will drive the development and optimization of filling system equipment, solve complex technical challenges, and guide systems from concept through commissioning, qualification, and successful line start‑up. This role offers the opportunity to influence critical technical decisions, partner closely with cross‑functional teams and vendors, and ensure the delivery of compliant, high‑performing filling systems that meet global regulatory expectations and support long‑term business success.

Requirements

Minimum of a Bachelor's Degree in engineering required (Mechanical Engineering preferred), MS or MBA preferred.
Minimum of 10 years of process engineering and/or capital project execution experience supporting aseptic filling systems for large‑molecule biotherapeutic drug products (vials and/or prefilled syringes) in a cGMP drug product manufacturing environment.
Demonstrated experience as a technical lead or subject matter expert (SME) for aseptic filling operations for sterile injectable biologics (e.g., monoclonal antibodies, recombinant proteins, vaccines).
Hands‑on experience leading the design, installation, commissioning, qualification (C&Q), and start‑up of aseptic filling line systems, including isolator‑based filling technologies.
Deep understanding of global aseptic manufacturing regulations, including FDA cGMPs and EU Annex 1, and their impact on facility, equipment, and process design.
Shown ability to lead and collaborate across cross‑functional teams (Manufacturing, MSAT, Quality, Facilities, EHS, Procurement, Engineering & Property Services) in a matrixed environment.
Extensive experience working with external partners (A&E firms, construction contractors, and equipment vendors) to develop, execute, and deliver complex capital projects.
Strong technical problem‑solving skills, with the ability to resolve sophisticated process, equipment, and regulatory challenges during project execution and C&Q.
Solid understanding of: Aseptic processing and contamination control strategies Commissioning & Qualification methodologies Engineering design principles for biotherapeutic drug product facilities Construction and procurement processes Project controls and project scheduling EHS requirements, including EHS‑by‑design and construction safety
Excellent communication, leadership, and decision‑making skills, with the ability to influence stakeholders and drive alignment in a fast‑paced, evolving business environment.
Strong passion for technical excellence and continuous improvement, with the ability to drive innovation in aseptic filling equipment and facilities.

Nice To Haves

Consistent track record leading large‑scale capital projects for aseptic filling systems with total project values in the range of $50M–$100M.
Experience supporting greenfield and/or brownfield GMP drug product manufacturing facility start‑ups.
Experience transitioning filling systems from conceptual design through operational readiness in a commercial biotherapeutic environment.

Responsibilities

Lead the development and delivery of aseptic filling line system documentation, including User Requirements Specifications (URS), equipment data sheets, technical specifications, P&IDs, and process flow diagrams (PFDs).
Evaluate and select equipment vendors by assessing technical capability, reviewing bid packages, and leading technical discussions; maintain accountability for filling system performance through project execution.
Lead the detailed design and engineering of aseptic filling line equipment (e.g., E‑Beam, isolators, vial and syringe filling lines) in close collaboration with equipment suppliers and cross‑functional stakeholders
Own the layout, design, and integration of the filling line within the facility, ensuring alignment with aseptic processing, Annex 1 requirements, and operational needs.
Serve as the technical lead for FAT, SAT, (C&Q), and start‑up of aseptic filling systems.
Lead technical issue investigation and resolution during C&Q and start‑up, ensuring systems are fully ready to enter qualification and routine operation.
Drive coordination and execution across multiple functions—Manufacturing, Facilities, MSAT, Quality, Procurement, Engineering & Property Services (E&PS), and EHS—to remove barriers and maintain project momentum.
Provide strong technical leadership and partner management, ensuring alignment across evolving business, quality, and regulatory expectations.
Stay ahead of on industry trends, regulatory changes, and external guidelines, benchmarking internal designs and approaches against leading standards.
Apply data‑driven insights and market intelligence to inform technical decisions, optimize system performance, and support long‑term portfolio and facility strategy.
Ensure all work follows company policies, cGMP requirements, global regulatory standards, and customer specifications.