Large

IPS-Integrated Project Services, LLC, a Berkshire Hathaway company, is a global leader in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities worldwide. With technical expertise spanning R&D to pilot-scale to large-scale production, our team specializes in the technology, trends, and regulatory environment to successfully deliver capital projects and improve operations. 

Headquartered in Pennsylvania, IPS is a multinational company with over 1,800 professionals and 23 offices in 10 countries in the United States, Canada, Brazil, the United Kingdom, Ireland, Germany, Switzerland, Singapore, China, and India. With the newest acquisition of Linesight, IPS has over 3,000 professionals in 45+ offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East. Linesight specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industrial.

Manufacturing & Electronics

IPS-Integrated Project Services

Life Sciences Consulting, Architecture, Engineering, Project Controls, Procurement, Construction Management, & CQV

You should have expertise in electrical design, project management skills, proficiency with relevant software, and the ability to collaborate with cross-functional teams to deliver effective solutions.

You will design electrical systems, collaborate with cross-functional teams, ensure compliance with codes, manage project timelines, and provide technical support throughout the project lifecycle.

Birmingham

Manchester

<div>
 Job Description: 
 <div>
   At IPS, your expertise, passion, and skills will contribute to solving complex challenges in pharmaceutical, biotech, and animal health research and manufacturing facilities. We are seeking an experienced <b>Senior Electrical Engineer</b> to lead our innovative electrical team in either <b>Cork or Dublin, Ireland, or Birmingham or Manchester, UK</b>.
 </div>
 <div></div>
 <div>
  <br> In this role, you will guide and expand a talented team of electrical engineers and designers dedicated to creating life-changing facilities. Mentorship is a key component of this position, as you will develop and retain this talented team, fostering an environment of continuous learning and growth.
 </div>
 <div>
   The ability to mentor others is crucial, as you will work to develop and retain this talented team.
 </div>
 <div></div>
 <div>
  <b><br> Key Responsibilities</b>
 </div>
 <ul>
  <li> Leadership &amp; Team Development: Lead a small team, mentor junior engineers, and ensure the team’s professional development.</li>
  <li> Project Management: Oversee the entire design process, act as a technical expert, and collaborate with Project Managers to define project scope, budget, and staffing needs.</li>
  <li> Planning &amp; Scheduling: Forecast work 12-16 weeks ahead, develop construction schedules, and manage resource allocation for multiple projects.</li>
  <li> Quality Assurance: Maintain high standards in design and production, ensuring all work meets company quality standards.</li>
  <li> Client Interaction: Build and maintain strong client relationships, ensuring satisfaction through regular communication and high-quality project delivery.</li>
  <li> Technical Expertise: Research design options, write electrical design scopes, prepare engineering studies, and create detailed schematic designs.</li>
  <li> Compliance &amp; Coordination: Ensure designs meet local codes and standards, estimate project costs, review contractor applications, and coordinate documentation.</li>
 </ul>
 <div></div>
 <div>
  <b><br> What We Offer</b>
 </div>
 <ul>
  <li> Flexibility: Choose to work from our offices in Cork, Dublin, Birmingham, or Manchester.</li>
  <li> Hybrid Work: 3 days in office, 2 days from home</li>
  <li> Impact: Work on projects that make a significant difference in the pharmaceutical and biotech industries.</li>
  <li> Growth: Opportunities for professional development and career advancement within a supportive and dynamic team environment.</li>
 </ul>
 <div>
   Come join a caring, nimble team that delivers world class designs for our pharmaceutical clients and take your career to new heights!
 </div> Qualifications &amp; Requirements: 
 <ul>
  <li>Bachelor of Engineering Degree in Electrical Engineering from an accredited university.</li>
  <li> Expertise in computer operation for engineering design programs and computer aided drafting (AutoCAD, Revit, etc.).</li>
  <li> Experience with design of building electrical systems, such as: building service, power distribution, generators, lighting, fire alarm, security and other low voltage systems.</li>
  <li> Has a strong understanding of the National Electric Code (NEC), NFPA 70E, NFPA 72, IBC and other related building codes and standards.</li>
 </ul>
 <div>
  <b> Preferred Qualifications</b>
 </div>
 <ul>
  <li> 10 years of experience in electrical design.</li>
  <li> Pharmaceutical, Biotech, Nutraceutical or Life Science industry experience.</li>
  <li> Experience with medium voltage systems, electrical hazardous classified areas, and telecommunications systems.</li>
 </ul> About Us: 
 <div>
   IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products. Its newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries. With the addition of Linesight, IPS has over 3,000 professionals in over 45 offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East.
 </div>
 <div></div>
 <div>
  <br> Specialties
 </div>
 <div></div>
 <div>
  <br> Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
 </div>
 <div></div>
 <div>
  <br> All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer.
 </div>
 <div></div>
 <div>
  <i><br> Attention Search Firms / Third-Party Recruiters: IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS. Regardless of past practice, all resumes submitted by search firms to any employee at IPS via email, the Internet, or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means.</i>
 </div>
</div>
<div></div>


 Job Description: 
 
   At IPS, your expertise, passion, and skills will contribute to solving complex challenges in pharmaceutical, biotech, and animal health research and manufacturing facilities. We are seeking an experienced Senior Electrical Engineer to lead our innovative electrical team in either Cork or Dublin, Ireland, or Birmingham or Manchester, UK.
 
 
 
   In this role, you will guide and expand a talented team of electrical engineers and designers dedicated to creating life-changing facilities. Mentorship is a key component of this position, as you will develop and retain this talented team, fostering an environment of continuous learning and growth.
 
 
   The ability to mentor others is crucial, as you will work to develop and retain this talented team.
 
 
 
   Key Responsibilities
 
 
   Leadership & Team Development: Lead a small team, mentor junior engineers, and ensure the team’s professional development.
   Project Management: Oversee the entire design process, act as a technical expert, and collaborate with Project Managers to define project scope, budget, and staffing needs.
   Planning & Scheduling: Forecast work 12-16 weeks ahead, develop construction schedules, and manage resource allocation for multiple projects.
   Quality Assurance: Maintain high standards in design and production, ensuring all work meets company quality standards.
   Client Interaction: Build and maintain strong client relationships, ensuring satisfaction through regular communication and high-quality project delivery.
   Technical Expertise: Research design options, write electrical design scopes, prepare engineering studies, and create detailed schematic designs.
   Compliance & Coordination: Ensure designs meet local codes and standards, estimate project costs, review contractor applications, and coordinate documentation.
 
 
 
   What We Offer
 
 
   Flexibility: Choose to work from our offices in Cork, Dublin, Birmingham, or Manchester.
   Hybrid Work: 3 days in office, 2 days from home
   Impact: Work on projects that make a significant difference in the pharmaceutical and biotech industries.
   Growth: Opportunities for professional development and career advancement within a supportive and dynamic team environment.
 
 
   Come join a caring, nimble team that delivers world class designs for our pharmaceutical clients and take your career to new heights!
  Qualifications & Requirements: 
 
  Bachelor of Engineering Degree in Electrical Engineering from an accredited university.
   Expertise in computer operation for engineering design programs and computer aided drafting (AutoCAD, Revit, etc.).
   Experience with design of building electrical systems, such as: building service, power distribution, generators, lighting, fire alarm, security and other low voltage systems.
   Has a strong understanding of the National Electric Code (NEC), NFPA 70E, NFPA 72, IBC and other related building codes and standards.
 
 
   Preferred Qualifications
 
 
   10 years of experience in electrical design.
   Pharmaceutical, Biotech, Nutraceutical or Life Science industry experience.
   Experience with medium voltage systems, electrical hazardous classified areas, and telecommunications systems.
  About Us: 
 
   IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products. Its newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries. With the addition of Linesight, IPS has over 3,000 professionals in over 45 offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East.
 
 
 
   Specialties
 
 
 
   Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
 
 
 
   All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer.
 
 
 
   Attention Search Firms / Third-Party Recruiters: IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS. Regardless of past practice, all resumes submitted by search firms to any employee at IPS via email, the Internet, or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means.
 



Senior Electrical Design Engineer - IPS-Integrated Project Services

Senior Electrical Design Engineer

You need 10+ years in engineering, a relevant degree, 3+ years with DCS/PLC/SCADA, 4+ years in Pharma instrumentation, plus expertise in ISA standards and cGMP documents. Travel required.

You will develop automation solutions, manage project tasks, collaborate with teams, create specifications, support system validation, and engage with clients and vendors for process control systems.

Engineering

Burlington

<p><strong>Job Description:</strong></p><ul><li>At IPS, you will apply your knowledge, skills, and passion to make a difference in the lives of people by solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities. We are looking for a dedicated<strong> Senior Process Automation Engineer</strong> to join our talented team at our office located in our <strong>Burlington, MA </strong>office location.</li><li>In this role, you will provide the project team with technical leadership, automation expertise, and instrumentation support for the design, engineering, construction, and qualification of Pharmaceutical and Biotech related projects.</li></ul><p><strong>Position Responsibilities:</strong></p><ul><li>Demonstrates subject matter expertise by developing department standards and improving existing work practices.</li><li>Manages and delegates tasks to meet project scope, schedule, and deadlines.</li><li>Assists clients in strategic evaluations to develop concepts supported by engineering studies for expanding, improving, or automating existing facilities.</li><li>Works with clients, other IPS disciplines, and vendors to develop complete Automation solutions.</li><li>Consulting on the proper adoption of the ISA S95 levels to meet the client’s needs now and in the future.</li><li>Actively collaborate with the process design and project teams to support the execution of successful project studies.</li><li>Develop the design and specifications for DCS, PLC, and SCADA-based process control systems for IPS clients and projects.</li><li>Perform automation-related job functions as assigned, including, I/O lists, Instrumentation lists, and the specification of instrumentation and control elements.</li><li>Support IQ/OQ development and participate in systems analysis, validation, and verification.</li><li>Identify, qualify, and collaborate with third-party system integrators as necessary to support project and company business objectives.</li><li>Work with end users and Original Equipment Manufacturers (OEMs) to coordinate the application of automation products.</li></ul><p>Come join a caring, nimble team that delivers world-class designs for our pharmaceutical clients and take your career to new heights!</p><p><strong>Qualifications &amp; Requirements:</strong></p><ul><li>10+ years of diversified engineering experience with in-depth knowledge of industry requirements and applications within the Process Automation market.</li><li>Bachelor’s degree in Engineering - ME/EE//ChemE/Automation/Manufacturing – or equivalent degree from an accredited university.</li><li>3+ years of experience with industrial process control systems including DCS, PLC, and SCADA-based systems.</li><li>4+ years of experience with Pharmaceutical process instrumentation.</li><li>Expertise in computer operation for engineering design programs and computer-aided drafting.</li><li>Experienced with ISA standards and the interpretation of P&amp;I drawings.</li><li>Experience with the development of cGMP and GAMP automation lifecycle documents.</li><li>Registered Professional Engineer preferred.</li></ul><p><strong>Context, Environment, &amp; Safety:</strong></p><ul><li>Travel based on the project location.</li></ul><p>This position is a safety-sensitive position. The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.</p>

Job Description:At IPS, you will apply your knowledge, skills, and passion to make a difference in the lives of people by solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities. We are looking for a dedicated Senior Process Automation Engineer to join our talented team at our office located in our Burlington, MA office location.In this role, you will provide the project team with technical leadership, automation expertise, and instrumentation support for the design, engineering, construction, and qualification of Pharmaceutical and Biotech related projects.Position Responsibilities:Demonstrates subject matter expertise by developing department standards and improving existing work practices.Manages and delegates tasks to meet project scope, schedule, and deadlines.Assists clients in strategic evaluations to develop concepts supported by engineering studies for expanding, improving, or automating existing facilities.Works with clients, other IPS disciplines, and vendors to develop complete Automation solutions.Consulting on the proper adoption of the ISA S95 levels to meet the client’s needs now and in the future.Actively collaborate with the process design and project teams to support the execution of successful project studies.Develop the design and specifications for DCS, PLC, and SCADA-based process control systems for IPS clients and projects.Perform automation-related job functions as assigned, including, I/O lists, Instrumentation lists, and the specification of instrumentation and control elements.Support IQ/OQ development and participate in systems analysis, validation, and verification.Identify, qualify, and collaborate with third-party system integrators as necessary to support project and company business objectives.Work with end users and Original Equipment Manufacturers (OEMs) to coordinate the application of automation products.Come join a caring, nimble team that delivers world-class designs for our pharmaceutical clients and take your career to new heights!Qualifications & Requirements:10+ years of diversified engineering experience with in-depth knowledge of industry requirements and applications within the Process Automation market.Bachelor’s degree in Engineering - ME/EE//ChemE/Automation/Manufacturing – or equivalent degree from an accredited university.3+ years of experience with industrial process control systems including DCS, PLC, and SCADA-based systems.4+ years of experience with Pharmaceutical process instrumentation.Expertise in computer operation for engineering design programs and computer-aided drafting.Experienced with ISA standards and the interpretation of P&I drawings.Experience with the development of cGMP and GAMP automation lifecycle documents.Registered Professional Engineer preferred.Context, Environment, & Safety:Travel based on the project location.This position is a safety-sensitive position. The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.

Senior Process Automation Engineer - IPS-Integrated Project Services

<div>
 Job Description: 
 <div>
   At IPS, you will apply your knowledge, skills, and passion to make a difference in the lives of people by solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities. We are looking for a dedicated<b> Senior Process Automation Engineer</b> to join our talented team at our office located in our <b>Burlington, MA </b>office location.
 </div>
 <div></div>
 <div>
  <br> In this role, you will provide the project team with technical leadership, automation expertise, and instrumentation support for the design, engineering, construction, and qualification of Pharmaceutical and Biotech related projects.
 </div>
 <div></div>
 <div>
  <b><br> Position Responsibilities</b>
 </div>
 <ul>
  <li> Demonstrates subject matter expertise by developing department standards and improving existing work practices.</li>
  <li> Manages and delegates tasks to meet project scope, schedule, and deadlines.</li>
  <li> Assists clients in strategic evaluations to develop concepts supported by engineering studies for expanding, improving, or automating existing facilities.</li>
  <li> Works with clients, other IPS disciplines, and vendors to develop complete Automation solutions.</li>
  <li> Consulting on the proper adoption of the ISA S95 levels to meet the client’s needs now and in the future.</li>
  <li> Actively collaborate with the process design and project teams to support the execution of successful project studies.</li>
  <li> Develop the design and specifications for DCS, PLC, and SCADA-based process control systems for IPS clients and projects.</li>
  <li> Perform automation-related job functions as assigned, including, I/O lists, Instrumentation lists, and the specification of instrumentation and control elements.</li>
  <li> Support IQ/OQ development and participate in systems analysis, validation, and verification.</li>
  <li> Identify, qualify, and collaborate with third-party system integrators as necessary to support project and company business objectives.</li>
  <li> Work with end users and Original Equipment Manufacturers (OEMs) to coordinate the application of automation products.</li>
 </ul>
 <div>
   Come join a caring, nimble team that delivers world-class designs for our pharmaceutical clients and take your career to new heights!
 </div> Qualifications &amp; Requirements: 
 <ul>
  <li>10+ years of diversified engineering experience with in-depth knowledge of industry requirements and applications within the Process Automation market.</li>
  <li> Bachelor’s degree in Engineering - ME/EE//ChemE/Automation/Manufacturing – or equivalent degree from an accredited university.</li>
  <li> 3+ years of experience with industrial process control systems including DCS, PLC, and SCADA-based systems.</li>
  <li> 4+ years of experience with Pharmaceutical process instrumentation.</li>
  <li> Expertise in computer operation for engineering design programs and computer-aided drafting.</li>
  <li> Experienced with ISA standards and the interpretation of P&amp;I drawings.</li>
  <li> Experience with the development of cGMP and GAMP automation lifecycle documents.</li>
  <li> Registered Professional Engineer preferred.</li>
 </ul>
 <div>
  <b> Context, Environment, &amp; Safety</b>
 </div>
 <ul>
  <li> Travel based on the project location.</li>
 </ul>
 <div>
   This position is a safety-sensitive position. The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.
 </div> About Us: 
 <div>
   IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products. Its newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries. With the addition of Linesight, IPS has over 3,000 professionals in over 45 offices across 17 countries in the Americas, Europe, Asia Pacific, Southeast Asia, Australia, and the Middle East.
  <br> 
  <br> <b>Specialties</b>
  <br> 
  <br> Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
  <br> 
  <br> All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer.
  <br> 
  <br> Attention Search Firms / Third-Party Recruiters: IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS. Regardless of past practice, all resumes submitted by search firms to any employee at IPS via email, the Internet, or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means.
 </div>
 <div></div>
 <div>
  <br> #LI-KZ1
 </div>
</div>

Senior Process Automation Engineer

You need a BS in Engineering, 7+ years in Pharma/Biotech, and experience with GMP validation protocols. Expect up to 100% travel and adherence to site safety rules.

You will write C/Q/V documents, perform FATs/SATs, execute protocols, verify system drawings, compile reports, troubleshoot issues, and ensure compliance in pharmaceutical projects.

Houston

<p><strong>Job Description:</strong></p><ul><li>At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a talented <strong>Senior Validation Engineer </strong>to join our team at a project site located in <strong>Houston, Texas!</strong></li><li>In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. Additionally, you will follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements. You may also perform standalone commissioning services for non-FDA-regulated clients.<strong> </strong></li></ul><p><strong>What You'll Do:</strong></p><p>Write C/Q/V documents following established standards and templates, including but not limited to the following:</p><ul><li>Commissioning Forms</li><li>C/Q/V Protocols and Summary Reports</li><li>Standard Operating Procedures</li><li>Impact Assessments</li><li>Specifications (URS/FRS/DDS)</li><li>FATS/SATs</li></ul><p>Perform field/site activities including, but not limited to, the following:</p><ul><li>Attend and witness FATs and SATs as a representative of IPS clients.</li><li>Execution of commissioning forms and witnessing vendor start-up and testing.</li><li>Execution of C/Q/V protocols.</li><li>Walkdown and verification of system drawings (P&amp;IDs, as-builts, etc.)</li><li>Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc.</li><li>Assist in deviation investigation and resolution of problems and issues encountered during field execution activities.</li><li>Work with the Project Delivery department or CM for start-up and vendor testing. Witness and troubleshoot as required.</li><li>Perform C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries.</li><li>Read, understand, and utilize the IPS Best Practices and SOPs for the delivery of compliance services</li><li>Perform work to meet IPS budget requirements and quality standards.</li><li>Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management, of project status and issues, as needed.</li></ul><p><strong>Qualifications &amp; Requirements:</strong></p><ul><li>Bachelor of Science in Engineering.</li><li>7 or more years of relevant experience.</li><li>Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.</li></ul><p><strong>Preferred Qualifications:</strong></p><ul><li>Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software.</li><li>Has general exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.</li></ul><p>Context &amp; Safety:</p><ul><li>This position will have up to 100% travel to the site, or as required by the assigned project.</li><li>You may be assigned to a client site for an extended period.</li><li>Overnight travel or staying in the city of the Client’s location is possible depending on the assignment.</li><li>Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan.</li><li>You may visit active construction sites and will be required to take site safety training and adhere to site safety rules.</li><li>This position is a safety-sensitive position.</li><li>The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.</li></ul>

Job Description:At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a talented Senior Validation Engineer to join our team at a project site located in Houston, Texas!In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. Additionally, you will follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements. You may also perform standalone commissioning services for non-FDA-regulated clients. What You'll Do:Write C/Q/V documents following established standards and templates, including but not limited to the following:Commissioning FormsC/Q/V Protocols and Summary ReportsStandard Operating ProceduresImpact AssessmentsSpecifications (URS/FRS/DDS)FATS/SATsPerform field/site activities including, but not limited to, the following:Attend and witness FATs and SATs as a representative of IPS clients.Execution of commissioning forms and witnessing vendor start-up and testing.Execution of C/Q/V protocols.Walkdown and verification of system drawings (P&IDs, as-builts, etc.)Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc.Assist in deviation investigation and resolution of problems and issues encountered during field execution activities.Work with the Project Delivery department or CM for start-up and vendor testing. Witness and troubleshoot as required.Perform C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries.Read, understand, and utilize the IPS Best Practices and SOPs for the delivery of compliance servicesPerform work to meet IPS budget requirements and quality standards.Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management, of project status and issues, as needed.Qualifications & Requirements:Bachelor of Science in Engineering.7 or more years of relevant experience.Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.Preferred Qualifications:Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software.Has general exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.Context & Safety:This position will have up to 100% travel to the site, or as required by the assigned project.You may be assigned to a client site for an extended period.Overnight travel or staying in the city of the Client’s location is possible depending on the assignment.Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan.You may visit active construction sites and will be required to take site safety training and adhere to site safety rules.This position is a safety-sensitive position.The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.

IPS-Integrated Project Services

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