Senior Control Systems Engineer

2 weeks ago


Carlsbad, United States Novartis Group Companies Full time
Benefits:
Parental leave, paid time off, sick time, 401(k)

Position Overview:

The Senior Automation Engineer plays a crucial role in the integration of new process equipment while also ensuring the maintenance, troubleshooting, and enhancement of existing GMP and non-GMP control systems within a GMP Radioligand Therapies Production Facility.

At the AAA Carlsbad Site, the systems in place encompass plant-wide SCADA, third-party skid and stand-alone control systems, as well as various environmental controls such as freezers, air handlers, chillers, and Building Management Systems.


About Us:

At Advanced Accelerator Applications, a Novartis company, we are dedicated to pioneering advancements in nuclear medicine and providing the next generation of targeted radioligand therapy for cancer patients. We seek skilled Supply Chain professionals to help us achieve our ambitious objectives.


Key Responsibilities:

Your responsibilities will include, but are not limited to:

  • Offering technical expertise in the design, configuration, installation, and upkeep of automation software and related hardware, while collaborating with other teams as needed.
  • Overseeing or participating in all automation aspects of upcoming projects, including the integration of third-party equipment into the plant DCS and BMS systems, data concentration, batch reporting, and data retention.
  • Providing support for 24/7 site-based operations post-startup.
  • Preparing scopes of work and leading automation contractors to ensure project timelines are met.
  • Developing project objectives in alignment with user requirements and business plans.
  • Determining specifications for equipment or systems and identifying the most cost-effective technologies for implementation.
  • Engaging in discussions with internal business partners regarding priorities and timelines, while promoting transparent information sharing.
  • Creating equipment specifications in standard documentation formats such as User Requirements (URS), Functional Specification (FS), and Detail Design Specifications (DDS/HDS/SDS).
  • Participating in operational excellence and continuous improvement initiatives.
  • Resolving any technical issues that may impact production.
  • Drafting and updating procedures to enhance operational efficiency and compliance.
  • Implementing and revising SOPs to align with established standards and policies.

Compensation:

The anticipated pay range for this position is between $107,200 and $160,800 annually; however, the base salary offered may vary based on individual factors such as market location, job-related knowledge, skills, and experience.

The total compensation package may also include additional elements such as a sign-on bonus, restricted stock units, and discretionary awards, along with a comprehensive range of medical, financial, and other benefits, including 401(k) eligibility and various paid time off benefits.


Minimum Qualifications:
  • Bachelor's degree in Computer Science, Information Technology, Automation, Engineering, or a related field.
  • A minimum of 5 years of relevant experience in Automation or IT within a GMP Pharma environment.
  • Extensive knowledge of automation systems and IT infrastructure.
  • Strong leadership and team management capabilities.
  • Preferred experience in aseptic environments.
  • Excellent communication and interpersonal skills.
  • Proven track record in managing budgets and project pipelines.
  • Familiarity with GMP regulations and compliance standards.
  • Able to collaborate effectively with cross-functional teams and key stakeholders.

Our Commitment:

At Novartis, we embrace diversity, equal opportunity, and inclusion. We are dedicated to building diverse teams that reflect the patients and communities we serve, fostering an inclusive workplace that promotes bold innovation through collaboration and empowers our employees to reach their full potential.



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