Operations Associate
$59.17k - $77.66kLegend Biotech US
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. Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, NJ. Role Overview This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations. Key Responsibilities * Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment. * Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum. * Execute manufacturing activities common to cell culturing, purification, aseptic processing, and cryopreservation using appropriate techniques. * Perform process unit operations according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP). * Perform tasks on time in a manner consistent with quality systems and cGMP requirements. * Work in a team based, cross-functional environment to complete production tasks required by shift schedule. * Aid in the development of manufacturing processes including appropriate documentation. * Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members.
- Handle human derived materials in containment areas.
- Support schedule adjustments to meet production.
- Accurately complete documentation in SOP’s, logbooks and other GMP documents.
- Demonstrate training progression through assigned curriculum.
- Accountable for maintaining a working knowledge of basic cGMP requirements to
- Ensure materials are available for production.
- Job duties performed routinely require exposure to and handling of biological
- Color Perception both eyes 5 slides out of 8.
- Report to work on-time and according to the shift schedule.
- Perform other duties as assigned.
- Attend departmental and other scheduled meetings.
- Practice good interpersonal and communication skills.
- Demonstrate positive team-oriented approach in the daily execution of
- Promote and work within a team environment.
- Learn new skills, procedures and processes as assigned by management and
- Support investigation efforts as required.
- Responsible for audit preparation and participation.
- Follow instructions.
- Solve practical problems and deal with a variety of concrete variables in
- Knowledge of Process Excellence Tools
- Possesses solid knowledge of routine and non-routine testing and sampling
- Is frequently required to communicate with coworkers.
- While performing the duties of this job, the employee is regularly required
- Ability to lift 25 lbs.
- Needs to perform gowning procedures to work in manufacturing core.
- Li-RN1
- Li-Onsite
$59,168—$77,658 USD
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech. Work Authorization & Employment Eligibility Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates. 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. For information related to our privacy notice, please review: Legend Biotech Privacy Notice [- ...shared responsibility and we work together to foster a culture where everyone belongs and is inspired to do their best work. As an Operations Specialist, you make sure that products flow smoothly through the store by maintaining product availability for customers,...SuggestedLocal areaRelocationNight shift
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