Responsibilities

This is a full-time salaried position withProject Farma, a PerkinElmer company. The successful candidate will reside in one of Project Farma's primary markets and be willing to travel domestically to meet client project requests.

Project Farma’s purpose is to improve patient lives by accelerating the delivery of life-changing therapies. We accomplish this through the successful execution of high-quality life sciences projects across the full project lifecycle. Project Farma (PF) team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management.

This role contributes to organizational success by supporting financial performance, operational efficiency, and continuous improvement, while also investing in people through mentorship, knowledge sharing, and professional development.

All team members are expected to embody Project Farma’s values by being curious, personable, and unselfish, while maintaining a strong commitment to a Patient Focused and People First mindset.

The Manager is responsible for leading a team and overseeing the execution of work aligned to project, client, and business objectives. This role balances people leadership with operational accountability, including coaching, performance management, resource planning, and ensuring high-quality delivery within defined scope, timelines, and budget.

As a Manager of Digital Transformation and Automation, you will own the delivery of projects or parts of a project and be responsible for Budget, Schedule and Quality of the project execution. You will manage the project team’s utilization, mobilization and demobilization. You will be responsible for managing the day-to-day client relationships for the assigned projects. You will have a business development aspect to the role to try and expand the services that PF can deliver to the client

Key Responsibilities

The DT&A Manager provides subject matter expertise in the design, implementation, and lifecycle management of automation systems across biologics, pharmaceutical, and novel therapy manufacturing facilities. This role requires deep experience with DCS/PLC/BMS/EMS platforms and the ability to author, interpret, and lead documentation such as URS, FRS, Functional Narratives, and detailed system architecture designs.

• Automation Design & Architecture
  • Develop full automation system architectures for biologics, pharmaceutical, and advanced therapy manufacturing facilities (DCS, PLC/SCADA, MES, historians, network layers, field instrumentation).
  • Create ISA‑88/ISA‑95‑aligned architecture diagrams, I/O strategies, network topologies, and interface specifications.
  • Ensure architecture supports scalability, cybersecurity, data integrity, and multi‑product flexibility.
• URS / FRS / Design Documentation
  • Lead the creation, review, and approval of:
  • URS (User Requirements Specifications)
  • FRS (Functional Requirements Specifications)
  • DS / DDS (Design Specifications)
  • Functional & Control Narratives
  • Recipe Design Documentation (ISA‑88 compliant)
  • Automation Standards & Engineering Guidelines
  • Work cross functionally to translate process requirements into robust automation design documents.
• Automation Implementation
  • Configure, program, and deploy DCS/PLC (modules, phases, recipes, batch strategies, graphics, alarms).
  • Support integration of OEM skids: bioreactors, chromatography systems, filtration skids, CIP/SIP, and fill finish equipment, HVAC, Chillers, Boilers, etc.
• Commissioning, Validation & GMP Compliance
  • Detailed knowledge of FAT, SAT, IQ/OQ, and PQ protocols in alignment with GAMP 5 and 21 CFR Part 11.
  • Ensure automation changes meet data integrity requirements, change control processes, and validation lifecycle rules.
  • Lead deviation investigations, CAPAs, and risk assessments related to automation systems.
• Manufacturing & Operations Support
  • Serve as SME for troubleshooting, system optimization, alarm tuning, batch failure analysis, and performance enhancements.
  • Support 24/7 operations through structured root cause analysis and resolution of automation issues.
  • Develop long-term automation lifecycle plans for upgrades, patches, and system expansions.
• Cross Functional Leadership‑Functional Leadership
  • Collaborate with IT/OT, process engineering, quality, and capital project teams to deliver integrated automation solutions.
  • Manage vendors, system integrators, and OEMs; review design packages and ensure alignment with internal standards.
  • Mentor junior engineers and act as technical SME during audits and regulatory inspections.

Attributes for Success

• Technical Delivery: Applies advanced technical knowledge and professional expertise
• Innovation & Continuous Improvement: Seeks better ways, adapts to change and champions new ideas.
• Customer Focus & Professionalism: Represents PF with consistent professionalism, appropriate escalation and respect for internal stakeholders, even during high stress delivery situations
• Integrity & Humility: Demonstrates self-awareness and puts PF mission above ego
• Collaboration & Communication: Communicates clearly and proactively and drives transparent alignment with clients.
• Project Execution: Delivers reliably, manages priorities and drives for high quality outcomes
• Growth Mindset: Shows openness to new ideas, feedback and change

Experience Required

• Education: Bachelor’s Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience.
• 10-15 years of experience
• Strong understanding of ISA‑88 batch control, ISA‑95 manufacturing hierarchy, BACnet, ISO 16484 and GAMP 5.
• PLC/DCS
  • 4+ years / 7+ years in automation engineering within GMP life sciences (biotech, pharma, ATMP). Expert-level experience with DeltaV DCS and/or Rockwell / Allen Bradley PLC/SCADA platforms.
• BMS/EMS
  • 4+ years / 7+ years in building automation engineering within GMP life sciences (biotech, pharma, ATMP). Expert-level experience with common BMS and EMS platforms (Siemens Desigo CC, Rockwell PLC, Schneider Electric, etc)
• Willingness to travel as required for client project assignments.

Other Preferred

• Strong communicator and influencer across engineering, quality, IT/OT, and manufacturing.
• Structured thinker with advanced troubleshooting and problem-solving skills.
• Skilled at managing multiple priorities in a high pressure, regulated environment.
• Ability to manage scope and track project changes
• Demonstrated leadership and mentorship abilities.

Project Farma is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.

The annual compensation range for this full-time position is $125,000 - 150,000. The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.