Control Systems Automation Specialist

2 weeks ago


Devens, Massachusetts, United States Veranova L P Full time
Job Overview

Company Overview

Veranova is a prominent entity in the realm of complex active pharmaceutical ingredient (API) development and manufacturing, catering to the needs of pharmaceutical and biotech clients. Our extensive technical knowledge and remarkable adaptability empower us to create innovative solutions and processes that foster and expedite advancement.

Position Summary

This role entails the comprehensive management, maintenance, oversight, and evaluation of automation and control system initiatives across Veranova's New England facilities. The individual in this position will act as the technical lead for automation and control-related capital projects and may engage in project management responsibilities. Additional duties encompass providing plant support by acquiring a thorough understanding of all control systems and pinpointing areas for enhancement; aiding in the training of operational and maintenance staff; and offering guidance in troubleshooting and optimizing all control systems. Furthermore, the role includes maintaining and updating control system documentation.

Key Responsibilities

  • Supervise all stages of automation and control project design activities.
  • Draft controls segments of User Requirement Documents for all initiatives.
  • Evaluate safety instrumented systems and design safety-rated interlock systems.
  • Compile detailed requests for proposals for all control project endeavors.
  • Oversee external contractors engaged to fulfill projects within designated timelines and budgets.
  • Manage all plant floor-level control systems and organize architectures, programming, and control systems for upcoming projects.
  • Act as the facility authority on all plant control systems to facilitate effective in-house troubleshooting and updates without the need for external resources.
  • Engage in continuous process improvement initiatives, including reducing utility consumption.
  • Maintain and refresh all automation and control system documentation, encompassing both hardware and software.
  • Establish a database for current and archived automation programs.
  • Create standards for automation and communication protocols.
  • Formulate and uphold master plans for automation on-site.
  • Develop and sustain software backup and recovery systems.
  • Implement cGMP principles in relation to department-specific responsibilities.
  • Ensure all documentation produced adheres to cGMP standards.
  • Contribute to audit preparedness and participate in quality audits with regulatory agencies and clients as necessary.
  • Perform any other tasks within the employee's skill set as reasonably instructed.

Qualifications

  • Bachelor's degree in chemical or electrical engineering (or a related discipline) is required, with a minimum of 5 years of experience, or at least 10 years of practical experience.
  • Proficiency in the operation, maintenance, troubleshooting, and programming of PLCs, HMIs, and DCS is essential.
  • Experience with DeltaV DCS, Allen Bradley PLCs, and/or Siemens PLCs is highly preferred.
  • Background in process control and automation with project management experience in the pharmaceutical sector is advantageous.
  • Expertise in diagnosing issues and replacing components in low voltage control panels (relays, switches, PLCs, modules, instruments) is required.
  • Thorough understanding of technical concepts, practices, and procedures in bulk pharmaceutical manufacturing and related support systems is strongly preferred.
  • Proficient in Microsoft Office applications (Outlook, Word, Excel, Project, and Visio) is essential.
  • Ability to read and comprehend repair manuals, specifications, drawings, and schematic diagrams accurately and promptly.
  • Exceptional verbal and written communication skills, including technical writing, are mandatory.
  • Strong organizational skills and attention to detail are essential.

Additional Information

All information will be kept confidential in accordance with EEO guidelines.

Veranova is an Equal Opportunity Employer, committed to providing equal employment access and opportunities to all individuals regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.

All applications are thoroughly reviewed, and your details will be securely stored in our Application Management System, which is utilized throughout Veranova for selecting suitable candidates for available positions. Veranova respects your privacy and is dedicated to safeguarding your personal information. For more details on how your personal data is utilized, please refer to our privacy notice.



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