About The Client
They are a global software and engineering consulting firm providing professional services in: Automation, Manufacturing Execution Systems (MES), and Smart Manufacturing. With combined 20+ years of experience in cGMP and FDA regulated industries, their growing and dedicated team of engineers continue to deliver innovative automation related solutions and expertise to plan, design, implement, and maintain projects in alignment with industry standards. They provide professional support and companionship for consulting services, project governance, and accelerating customer solutions in Automation, Manufacturing Systems & Information Technology. They provide client services that include Automation & IT Strategy, Concept Design, Project Execution, Service & Support, Life Cycle Planning & Optimization Services.
Responsibilities
- Implement capital automation projects using industry best practices and client business processes.
- Support the scope, deliverables, schedule, and project team for capital expenditure (CapEx) of automation projects.
- Participate in the development and evaluation of RFP and bidder/vendor analysis for General contracting and engineering services when design build method used.
- Identify and oversee system integrations.
- Ensure consultants & contractors working on any automation related projects maintain compliance with all GMP requirements (including training), EHS&S and security requirements, including completion and review of Job Hazard Assessments and client policies.
- Coordinate/support engineering and automation design, commissioning, qualification, and the QA Validation groups as appropriate.
- Proactively look for and recommend improvements in site processes and procedures.
- Represent the Capital Project Automation group with good communication and presentation skills.
Qualifications
- Bachelor's University degree in a Construction or Engineering related field.
- 10+ years of Automation Engineering experience preferably in pharmaceutical or Biotech industry
- Experience in Emerson DeltaV Process Control System (PCS)
- Solid understanding of GMP, GLP, and non-GMP project requirements
- Strong verbal and written communications skills.
- Flexible to work outside the core business hours (occasionally on short notice, and a limited basis) as needed.
- Ability to work well in a fast-paced team environment within a rapidly evolving business environment.
- Able to read and understand engineering plans and specifications.
Additional Details
-Employment Type: Full time with the Consultancy
-Client Location: US
-Candidate Location: Boston
