Sr Process Engineer (Hybrid - Gent)
Sr Process Engineer (Hybrid - Gent)
Apply remote type Hybrid Work locations BE022 GENT time type Full time posted on Posted 3 Days Ago time left to apply End Date: March 18, 2025 (10 days left to apply) job requisition id 2506239237W
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
Job Function: Supply Chain Engineering
Job Sub Function: Process Engineering
Job Category: Scientific/Technology
All Job Posting Locations: BE022 GENT
Job Description:
CAR-T is an innovative treatment, which uses the power of the patient’s own immune system. Patient’s T-cells are genetically modified to eliminate cancer cells. This ground-breaking technology provides hopeful prospects to patients where other therapies have failed or fail to provide adequate results.
Janssen Biotech, Inc. entered into a global collaboration agreement with Legend Biotech to develop, manufacture and commercialize (CAR) T-cell therapy. This partnership is designed to combine the strengths and expertise of two companies to deliver on the promise of a CAR T platform for immunotherapy and investigational treatment.
To support the CAR-T program in EMEA, we are working with great enthusiasm on expanding our capacity. The Process Engineer is part of the Manufacturing Science and Technology (MSAT) team. You will have the unique opportunity to gain deep knowledge & expertise in a highly innovative and future-oriented environment with the ability to profoundly impact the trajectory of health of our patients.
Key Responsibilities:
* Ensure process robustness by owning the process knowledge of the cell and gene therapy manufacturing process technology and providing scientific and technical expertise.
* Design studies necessary to successfully implement/validate the manufacturing process.
* Support and ensure cGMP readiness of the product process through an appropriate validation strategy in compliance with regulations, procedures, and the validation master plan.
* Serve as Subject Matter Expert (SME) in preparation for and during internal and external regulatory audits.
* Provide scientific support.
* Identify opportunities for continuous process improvements/operational excellence. Partner with all relevant teams and/or external vendors to implement process improvements.
Experience:
* You have a Master’s Degree in a scientific or technical field (Engineering, Science or related field) or equivalent experience.
* Minimum 5 years of relevant work experience in the biotech/biopharma industry.
* Cell and Gene Therapy manufacturing experience preferred.
Skills:
* You have a start-up/can-do mindset, and you proactively search for solutions.
* Your verbal and written communication skills enable you to influence without authority.
* You have strong analytical, problem-solving, and critical thinking skills.
* You thrive in a rapidly changing environment and lead as a change agent to promote flexibility, creativity, and accountability while at the same time handling procedures/guidelines which require strict execution.
* You work independently under general direction, having a good sense of prioritization and managing multiple tasks simultaneously.
Our Offer:
The opportunity to participate in a progressive treatment that gives hope to patients in need.
The ability to shape a new venture from the start and work in an innovative working environment.
Opportunities to continue to develop and grow in an extensive and strong organization.
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