Process Engineer

Posted 6 Days Ago
Be an Early Applicant
28 Locations
Remote
Junior
Healthtech • Pharmaceutical
The Role
The Process Engineer will design and specify cGMP process equipment, manage small-to-medium scale projects, participate in design reviews, and support QA Validation. Responsibilities also include revising diagrams, investigating control system issues, implementing process improvements, and ensuring compliance with relevant laws.
Summary Generated by Built In

 

**Project / Process Engineer**


About CAI

 

CAI is a dynamic, 100% employee-owned company founded in 1996, that has grown year over year to now encompass over 800 employees globally. We specialize in providing Commissioning, Qualifications, Validation, start-up, project management, and consulting services across FDA regulated and other mission-critical industries.

 

Our Commitment to Excellence

 

At CAI, our unwavering commitment is to prioritize our clients' interests. We persist until we achieve excellence, going above and beyond to deliver exceptional results. As CAI owners, we uphold our Foundational Principles both professionally and personally:

 

· Integrity: We act with the utmost integrity.

· Service: We serve one another and society.

· Sustainability: We work for our future.

 

We firmly believe that in employee ownership, individual success translates into collective success. We relentlessly pursue team objectives, valuing teamwork, respect for others, and a positive can-do attitude. This synergy has driven our exponential growth.

 

Position Overview

 

We are currently seeking a talented Process Engineer with 2-5 years’ experience to join our expanding operations in Ireland. In this role at CAI Ireland, you will:

 

· Specifies and designs cGMP process equipment, piping, and control systems.

· Manages projects of small-to-medium scale related to process equipment and manufacturing.

· Participates in design reviews, site acceptances, and equipment installation.

· Revises piping and instrumentation diagrams (P&ID) and associated drawings.

· Revises Process Flow Diagrams for manufacturing operations.

· Supports the QA Validation department by preparing design documents and assisting in protocol execution.

· Investigates process equipment, utility systems, control system issues, and safety incidents.

· Implements corrective and preventative actions for current equipment and processes.

· Implements improvements for manufacturing processes and utilities.

· Prepares engineering evaluations and test plans, and carries out change control documentation.

· Supervises mechanical, electrical, and automation contractors when needed.

· Ensures a clean and safe working environment by enforcing procedures, policies, and regulations.

· Upholds company reputation by ensuring compliance with all relevant laws, policies, and regulations.

· Identifies opportunities for equipment improvements and the adoption of new technologies.

· Assists with tech transfer activities, including process scale-up and New Product Introductions (NPIs).

 

 

Position Requirements

 

To thrive in this role within CAI Ireland, you will need:

 

· Requires a BS/BEng in Chemical, Process, or Mechanical engineering with 2-5 years of related experience. Direct experience with biopharmaceutical process equipment is preferred. Relevant experience may substitute for educational requirements.

· Experience in design and commissioning within the biopharmaceutical sector is desirable.

· Knowledgeable in CIP systems, bioreactors, centrifuges, chromatography, and ultrafiltration/diafiltration

· Strong problem-solving abilities aligned with Irelands regulatory standards.

· A strong customer-service focus, understanding the Irish market's unique needs.

· Willingness and flexibility to travel within Ireland potentially internationally if required.

 

 

Top Skills

Chemical
Mechanical
Process
The Company
HQ: Indianapolis, IN
923 Employees
On-site Workplace
Year Founded: 1996

What We Do

Fundamentally we exist for one reason: To be the trusted solution for our clients as they strive to build a better working world and improve the human experience.

We are 800+ global experts that bring top-tier expertise to every stage of a project, from creating comprehensive, detailed project plans to eliminating that last punch list item and beyond, into rigorous asset management, reliability, and sustainability activities. We are your choice regardless of your location.

Philosophically and practically, we believe that quality, cost, and schedule can be mutually reinforcing – trade-offs are not necessary. Short-changing the focus on quality usually means problems down the road – problems that can cost money and delay the schedule. But if quality is built in from the start, then both project delivery and operational efficiency can be achieved with a much higher degree of assurance.

When your project requires planned, managed, and documented high quality to exacting global standards. When you need high-performance teams on mission-critical projects. When your project is complex, high-visibility, and carries significant risk. We can help you meet a higher standard.

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