Legend Biotech · 2 weeks ago
BAS/EMS Technician
Raritan, NJ
Full-time
Onsite
Entry, Mid Level
2+ years expLegend Biotech is a global biotechnology company focused on treating life-threatening diseases through advanced cell therapies. The BAS/EMS Technician will provide engineering support for building automation and controls systems in the manufacturing plant, ensuring compliance with cGMP requirements while managing day-to-day activities related to automation systems.
BiotechnologyHealth CareLife ScienceOncologyTherapeutics
Responsibilities
Works with above plant functions to successfully implement and maintain tools, standards, policies and procedures in compliance
Handling day-to-day activities for BAS, EMS and other automation and controls system software, hardware and associated interfaces inclusive of data management, issues, deviations, corrections, remediation and improvement
Conducts local system data performance monitoring and analysis for BAS and EMS
Executes against SOPs, inclusive of data backup, disaster recovery, user administration, etc
Implements and maintains network configuration for BAS, EMS, and facility automation equipment
Provides training to end users
Provides user defined reports and facilitates ad-hoc queries
Provides status reports and coordinates with other departments or outside contractors/vendors to complete tasks
Qualification
Required
A minimum of 2 years as an automation and controls field service technician
Experience troubleshooting complex systems is a must
Deep knowledge of Honeywell and Siemens BAS software, hardware, protocols and IT infrastructure (HC900s, CPO, PXCMs, EBI, Desigo, BACnet, MODBUS, APOGEE P2)
Working in an aseptic manufacturing facility, preferably cell therapy, testing facility, quality assurance, or manufacturing compliance
Expertise in GMP compliance knowledge including knowledge of 21 CFR Part 11, EU Annex 11 among others
Experience with ICH and/or 21 CFR parts 210, 211, 1271 is required
Thorough knowledge and understanding of GMP data integrity standards
Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices
Strong interpersonal and written/oral communication skills
Ability to quickly process complex information and often make critical decisions with limited information
Proficient in applying process excellence tools and methodologies
Ability to independently be responsible for a portfolio of ongoing projects
Ability to pay attention to details and follow the procedures
The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision
Good written and verbal communication skills are required
Ability to summarize and present results, and experience with team-based collaborations is a requirement
Ability to work with others in a team environment
Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) and current Good Tissue Practices (cGTP) related to CAR-T manufacturing or cell processing
Ability to identify/remediate gaps in processes or systems
Experience authoring and executing documentation including but not limited to: Batch Records, SOPs, Work Instructions, protocols
Experience with BAS, EMS, TrackWise, CMMS and Maximo
Familiarity with IT application design and deployment
Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)
Preferred
Experience with 600, 601, and 610 is preferred
Benefits
Medical, dental, and vision insurance
401(k)-retirement plan with company match that vest fully on day one
Equity and stock options
Eight weeks of paid parental leave after just three months of employment
Paid time off policy that includes vacation days, personal days, sick time, 11 company holidays, and 3 floating holidays
Flexible spending and health savings accounts
Life and AD&D insurance
Short- and long-term disability coverage
Legal assistance
Supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance
Commuter benefits
Family planning and care resources
Well-being initiatives
Peer-to-peer recognition programs
Company
Legend Biotech
Legend Biotech is a biopharmaceutical company that develops and commercializes novel cell therapies for oncology.
1001-5000 employees
H1B Sponsorship
Legend Biotech has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (30)
2024 (11)
2023 (14)
2022 (7)
2021 (6)
2020 (13)
Funding
Current Stage
Public CompanyTotal Funding
$750.45M2023-05-05Post Ipo Equity· $350M
2022-07-25Post Ipo Equity· $250M
2020-06-05IPO
Leadership Team
Carlos Santos
Chief Financial Officer
Alan Bash
President, CARVYKTI
Recent News
2025-12-18
Company data provided by crunchbase