Sr. Automation Engineer

$112,800 - $112,800/Yr

Novartis - Carlsbad, CA

posted 4 months ago

Full-time - Mid Level
Carlsbad, CA
Chemical Manufacturing

About the position

The Senior Automation Engineer is a pivotal role within the Advanced Accelerator Applications, a Novartis company, focusing on the integration of new process equipment and the maintenance, troubleshooting, and modification of existing GMP and non-GMP control systems for a GMP Radioligand Therapies Production Facility. This position is critical in ensuring that the systems at the AAA Carlsbad Site, which include plant-wide SCADA, third-party skid and stand-alone control systems, freezers, air handlers, chillers, and Building Management Systems, operate efficiently and effectively. In this role, you will provide technical expertise for the design, configuration, installation, and maintenance of automation software and associated hardware. This includes collaborating with other teams to ensure seamless integration of automation systems. You will oversee or participate in all automation aspects of future projects, which will involve integrating third-party equipment into the plant DCS and BMS systems, data concentration, batch reporting, and data retention. Your support will be crucial for 24x7 site-based operations after startup, ensuring that all systems are functioning optimally. You will be responsible for preparing scopes of work and leading automation contractors to complete required work within project timelines. Developing project objectives in alignment with user requirements and business plans will be a key part of your responsibilities. You will also determine equipment or system specifications and identify the most cost-effective technology to implement. Engaging in discussions with internal business partners regarding priorities and timelines will be essential, as will the transparent sharing of information. Additionally, you will develop equipment specifications in standard documentation, including User Requirements (URS), Functional Specification (FS), and Detail Design Specifications (DDS/HDS/SDS). Your role will also involve participating in operational excellence and continuous improvement efforts, problem-solving any technical issues impacting production, and creating and updating procedures to drive operational efficiency and compliance. Implementing and revising SOPs to conform with standards and policies will be part of your ongoing responsibilities.

Responsibilities

  • Provide technical expertise for the design, configuration, installation, and maintenance of automation software and associated hardware.
  • Provide oversight or participation on all automation aspects of future projects including integration of 3rd party equipment to the plant DCS and BMS systems, data concentration, batch reporting, and data retention.
  • Support 24x7 site-based operations after startup.
  • Prepare scopes of work and lead automation contractors as required to complete required work within project timelines.
  • Develop project objectives working with user requirements and business plans.
  • Determine equipment or system specifications and most cost-effective technology to be implemented.
  • Participate in discussions with internal business partners on priorities and timelines, consistently supporting the transparent sharing of information.
  • Develop equipment specifications in standard documentation - User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS/HDS/SDS).
  • Participate in operational excellence and continuous improvement efforts.
  • Problem solve any technically related issues impacting production.
  • Create and update procedures to drive operational efficiency and compliance.
  • Implement and revise SOPs to conform with standards and policies.

Requirements

  • Bachelor's degree in Computer Science, Information Technology, Automation, Engineering or a related field is required.
  • 5+ years of relevant Automation or IT experience, in a GMP Pharma environment is required.
  • In-depth knowledge of automation systems and IT infrastructure.
  • Strong leadership and team management skills.
  • Previous aseptic experience is preferred.
  • Excellent communication and interpersonal skills.
  • Proven experience in managing budgets and project pipelines.
  • Familiarity with GMP regulations and compliance standards.
  • Ability to collaborate with cross-functional teams and key stakeholders.

Nice-to-haves

  • Previous aseptic experience is preferred.

Benefits

  • 401(k) eligibility
  • Various paid time off benefits, such as vacation, sick time, and parental leave
  • Sign-on bonus
  • Restricted stock units
  • Discretionary awards
  • Full range of medical benefits
  • Financial benefits.
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