Cell Therapy Automation Technician - MFG, QC, and Utilities equipment
About The Position
As Automation Technician specializing in Environmental/Equipment Monitoring System (EMS) and process equipment/systems, you will play an integral role in the Facilities and Engineering team to ensure reliable and compliant operations of a new Cell Therapy site and process equipment. This position reports to the Director of Engineering. Key Responsibilities: Support continuous improvement initiatives to optimize automation platforms and OT systems (for manufacturing and Quality control Lab equipment) and ensure alignment with operational cross-functional teams. This role will perform or support configuration, installation, startup, and operational readiness of all automation and OT platforms. Responsibilities include diagnosing and resolving technical issues related to computerized process equipment and control systems and ensuring compliance with industry regulations and standards. Perform as system admin for automation systems and OT / process equipment. Support developing budget estimates for capital equipment purchases and small projects. Execute preventative maintenance for automation and OT systems/equipment. As system admin or custodian, maintain validated or commissioned state of the systems. Perform other duties assigned by the Supervisor. Rotational on-call support is required.
Requirements
- Associate degree and minimum of 3 years of experience OR Bachelor’s degree and 1 year of experience. Technical and Engineering fields are preferred.
- Experience with facility environmental monitoring systems, building management systems, automation/OT for cell therapy process equipment (MFG and QC lab), or other related experience.
- Knowledge of GMP regulations, applicability to the management of automation and/or OT systems, and familiar working with process equipment vendors.
- Experience in system/equipment integration and networking principles within a GMP environment.
- Fixing and problem-solving skills with the ability to analyze complex system issues while adhering to GMP regulations.
- Excellent communication and collaboration skills to work effectively with multi-functional teams and stakeholders in a GMP environment.
Nice To Haves
- Experience with regulatory inspections and internal audits.
- Education in the Technical and Engineering fields preferred.
Responsibilities
- Support continuous improvement initiatives to optimize automation platforms and OT systems (for manufacturing and Quality control Lab equipment) and ensure alignment with operational cross-functional teams.
- Perform or support configuration, installation, startup, and operational readiness of all automation and OT platforms.
- Diagnosing and resolving technical issues related to computerized process equipment and control systems and ensuring compliance with industry regulations and standards.
- Perform as system admin for automation systems and OT / process equipment.
- Support developing budget estimates for capital equipment purchases and small projects.
- Execute preventative maintenance for automation and OT systems/equipment.
- As system admin or custodian, maintain validated or commissioned state of the systems.
- Perform other duties assigned by the Supervisor.
- Rotational on-call support is required.
Benefits
- qualified retirement programs
- paid time off (i.e., vacation, holiday, and leaves)
- health, dental, and vision coverage in accordance with the terms of the applicable plans
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
