R

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Senior Automation Manager - Systems Automation

Engineering LeadershipConfirmed live in the last 24 hours
Full-timeMenands, NY, USA$121.1k - $231k /yr

About the Job

Requirements

  • A Bachelor of Science degree in Engineering, Computer Science, or a related field is required.
  • For Manager level, at least 7 years of experience in the design, configuration, administration, and management of software, databases, and computerized systems is required.
  • For Senior Manager level, at least 8 years of relevant experience is required; level is determined based on qualifications.
  • Prior experience in a pharmaceutical or biopharmaceutical manufacturing facility is preferred.
  • A solid understanding of PI Historian and Rockwell applications is required.
  • Familiarity with PLC, HMI, historian, and product testing software is preferred.
  • Highly skilled ability to develop and edit Software Lifecycle Documentation, design documents, technical evaluations, and test plans following cGMP and GAMP 5 guidelines is preferred.

Responsibilities

  • Lead and develop a technical automation team, managing performance, development, and results while empowering team members to deliver under demanding timelines and situations.
  • Provide technical automation systems support to manufacturing and support areas; coordinate investigations of manufacturing deviations and anomalies related to automation systems, IT infrastructure, and software.
  • Lead corrective-action and systems-performance improvement projects; deliver large-scope projects requiring analysis of business metrics, including production, performance, and operational data.
  • Provide technical review of lifecycle documentation, software testing, and protocols; lead the team in supporting Quality Assurance with automated system test plan approval for change control and validation projects.
  • Create, maintain, and approve SOPs and Software Lifecycle Documentation; develop and edit design documents, technical evaluations, and test plans in accordance with cGMP and GAMP 5 guidelines.
  • Manage and maintain the project portfolio and work metrics, departmental data, and technical reports; communicate across engineering staff, cross-functional departments, and management.
  • Design, configure, and troubleshoot networked systems; balance changing priorities and increasing workload through timely decision-making and effective delegation.

Desired Qualifications

  • Prior experience in a pharmaceutical or biopharmaceutical manufacturing facility.
  • Familiarity with PLC, HMI, historian, and product testing software.
  • Highly skilled ability to develop and edit Software Lifecycle Documentation, design documents, technical evaluations, and test plans following cGMP and GAMP 5 guidelines.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

Recently Posted Jobs

Explore more opportunities at Regeneron Pharmaceuticals

See more jobs