Legend Biotech is seeking an Operations Process Trainer as part of the Technical Operations team based in Raritan, NJ.
Role Overview
The Operations Process Trainer will be responsible for performing training activities for Operations team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with Training team members in collaboration with management in Operations to support personalized cell therapy production through safe and compliant operations according to cGMP requirements. This individual will support organization build and ramp-up of clinical production and facility approval of a state of the art cell therapy facility for commercial launch and sustained production. The role will require technical experience, effective communication, coordination and collaboration across relevant cross functional groups to enable robust production, testing and release of product to patients.
1st Shift, Mon-Fri
Key Responsibilities
Leads, coaches and delivers a holistic, effective training program for Operations (Manufacturing, Warehouse, Facilities & Engineering, Validation, Technical Support, Supply Chain) that supports daily clinical production and strategically prepares for commercial supply of a CAR-T product
Manages, plans, coordinates, prepares and performs hands-on training curriculum in areas of general use, foundational and core skills, systems, unit operations and aseptic processing
Prepares and maintains training lab, materials and equipment
Conducts Observation, Side-by-Side, and Instructor Led Training
Conducts knowledge and skill checks and independent performance qualifications for Operations
Helps write or revise SOPs/Work Instructions, knowledge and skills assessments
Performs training assessments for new and updated procedures
Identifies technical training needs and expectations, monitors progress, addresses and resolves gaps in training requirements for Operations
Supports evaluation of appropriate compliance courses for Operations
Performs training for new hires
Optimizes the effectiveness and efficiency of training program in delivery of qualified personnel
Supports investigations and evaluates improvement opportunities for effective compliant training performance leading to sustained right first-time execution
Serve as subject matter expert for Compliance & Training systems
Knowledge of LMS system
Supports the maintenance and reporting of quality training metrics
Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals
Job duties include operating an industrial vehicle; Ability to lift a minimum of 50 lbs and stand for a long period of time
Distance visual acuity of at least 20/30 (Snellen) in both eyes without corrective lenses or visual acuity corrected to 20/30 (Snellen) or better with corrective lenses.
Requirements
A minimum of a Bachelor's Degree in Science, Information Science or equivalent technical discipline is required.
A minimum of 4 years relevant work experience is required. Candidate must have experience working within an aseptic manufacturing facility, preferably in training/system applications, quality systems, or learning management systems.
Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices
Experience with training methodology, adult learning theory, instructional design and Train-the-Trainer programs
Curriculum and module design experience
Advanced computer skills and practical knowledge of MS Office Suite, SharePoint, and other related systems
Good verbal and written communication skills
Excellent organizational skills
Ability to effectively prioritize and execute tasks in a fast-paced environment
Works well in a team-oriented, collaborative environment
The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision
Proactive and continuous improvement oriented
Ability to lead with influence
cGMP manufacturing
#Li-Onsite
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Benefits
Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Please note: These benefits are offered exclusively to permanent full-time employees. Contract employees are not eligible for benefits through Legend Biotech.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions.
For information related to our privacy policy, please review: Legend Biotech Privacy Policy.
Legend Biotech is a global clinical-stage biopharmaceutical company engaged in the discovery and development of novel cell therapies for oncology and other indications. Our team of over 1,000 employees across the United States, China and Europe, along with our differentiated technology, global development, and manufacturing strategies and expertise, provide us with the strong potential to discover, develop, and manufacture cutting edge cell therapies for patients in need.
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