Mark Chaumeton

Downstream Process Automation DeltaV Support Engineer – North Carolina – Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented Downstream Process Automation DeltaV Support Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. Essential Duties and Responsibilities for this role include, but are not limited to: Attend regularly scheduled project status meetings with Automation engineers and the System IntegratorInitiate design and provide input on Automation requirements for one or multiple process areasReview life cycle documentationInitiate and drive delivery of Automation changes in support of CAPEX project requirementsReview and approve Kneat documents including: DeltaV software FATs, Automation Commissioning Test Protocols, software OQs, and Automation Change Assessments.Support generation of Kneat documents. Requirements: Ability to own and implement Automation change controls independentlyExperience in a cGMP pharmaceutical facility working with FDA regulations is requiredWorking knowledge of Kneat validation software is requiredExcellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to managementExcellent interpersonal skills and ability to work effectively and efficiently in a team-based environment with employees at all levels If you are interested, please apply now for immediate consideration and further information. #LI-MC1

Upstream Process Automation DeltaV Support Engineer – North Carolina – Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented Upstream Process Automation DeltaV Support Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. Essential Duties and Responsibilities for this role include, but are not limited to: Attend regularly scheduled project status meetings with Automation engineers and the System IntegratorReview life cycle documentationInitiate and drive delivery of Automation changes in support of CAPEX project requirementsReview and approve Kneat documents including: DeltaV software FATs, Automation Commissioning Test Protocols, software OQs, and Automation Change Assessments.Support generation of Kneat documents.Manage/oversee the System Integrator’s delivery of DeltaV configuration for certain upstream process areas Requirements: Experience in a cGMP pharmaceutical facility is requiredWorking knowledge of lifecycle documentation and CSV concepts and principles is requiredExperience with Kneat validation software is desiredExcellent organizational, oral, and written communication skills and fluency in English with the ability to effectively communicate within cross-functional teams and to management If you are interested, please apply now for immediate consideration and further information. #LI-MC1

Instrumentation & Controls Project Lead - US, Raleigh - 12 Month ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Instrumentation & Controls Project Lead for their Raleigh based location.   What you'll do: Review design drawings, specifications, and technical documents to ensure accuracy and feasibility.Provide technical expertise to resolve design and implementation challenges.Identify and resolve technical issues that arise during installation and operational phases.Develop and implement corrective actions to address system discrepancies.Enforce strict adherence to safety regulations and procedures in all aspects of electrical and instrumentation work. What you'll need: Extensive experience in electrical and instrumentation systems construction within industrial or engineering projects, preferably in pharmaceutical, oil and gas, or manufacturing sectors.Experience with DeltaV system is a must. If this role is of interest to you, please apply now!#LI-SC1

Process Engineer - US, Texas - 3-12 Month ContractOur client is a global leader in the design and delivery of high-tech facilities for the life sciences sector. Specialising in sustainable, compliant, and future-ready solutions, they are looking for a Process Engineer to support their project based near Texas. This is a fantastic opportunity to join a forward-thinking team shaping the future of critical infrastructure. What you'll do: Develop, review, and update Process Flow Diagrams (PFDs) and Piping and Instrumentation Diagrams (P&IDs) for OSD manufacturing systems (granulation, blending, compression, coating, and encapsulation).Provide process design and engineering support for new facility installations, modifications, and technology transfers.Specify and select process equipment and instrumentation in collaboration with vendors and internal stakeholders.Lead and support commissioning, qualification, and validation (CQV) activities for process systems.Analyze process data to identify and implement continuous improvement initiatives that enhance efficiency, quality, and compliance. What you'll need: Bachelor’s or Master’s Degree in Chemical Engineering, Mechanical Engineering, or related discipline.Extensive experience in pharmaceutical or biopharmaceutical process engineering, preferably in Oral Solid Dosage (OSD) manufacturing.Proven experience developing and interpreting P&IDs and process documentation.Strong knowledge of GMP, FDA, and ICH guidelines.Experience with process design tools (e.g., AutoCAD, Visio, or similar). If this role is of interest, please apply now!#LI-MC1

Construction Turnover Lead - Raleigh, North Carolina - 3 Month Initial ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Construction Turnover Lead for their Raleigh based location.   What you'll do: Lead the turnover of mechanical, electrical, civil, and architectural systems from construction to commissioning or business operations, ensuring alignment with project scope and requirements.Manage and coordinate turnover activities, including walkdowns, punch list tracking, test pack reviews, and preparation of Turnover and Handover Dossiers.Liaise with different teams, commissioning, and end users to ensure timely sign-offs, documentation accuracy, and readiness for system handover.Chair weekly turnover meetings, issue progress reports, and analyze performance metrics such as punch list closure rates and documentation quality.Support electronic punch list tracking, ensure compliance with GDP, and act as Turnover Engineer when required. What you'll need: Requires extensive experience in the pharmaceutical or biotech industryExperience working with greenfield or brownfield projectsExperience with CM firms working as an owner’s representative If this role is of interest to you, please apply now!#LI-MC1

Building Safety Lead - US, Raleigh - Long Term ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Building Safety Lead for their Raleigh based location.  Essential Duties and Responsibilities for this role include, but are not limited to, the following: Provide field level supervision in support of construction safety, monitoring of assurance activities, maintaining performance metrics, ensuring implementation of construction safety processes and proceduresIdentify daily construction safety risks and work with teams to develop JHA (Job Hazard Analysis) and High Risk Activity management program.Assure that all contractors are implementing our strategy and safe working practices on siteEnsures that Contractors are implementing our clients and General Construction Safety Plan and Contractor’s Construction Safety Plan.Monitor and assess Contractors’ safety performance. Verify key performance indices (KPIs), leading/lagging indicators, and EHS data submitted by CM firm are accurate, timely and complete.Supports incident reviews, development of corrective action plans, and support escalation of all safety dataAssist and monitor the development and completion of corrective action plans with Contractor Desirable Experience: Requires extensive experience in the pharmaceutical or biotech industryExperience working with greenfield or brownfield projectsExperience with CM firms working as an owner’s representative If this role is of interest to you, please apply now!#LI-MC1

Engineering Project Director - US, North Carolina - Long Term Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented Engineering Project Director to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. Essential Duties and Responsibilities for this role include, but are not limited to: CQV focus, Engineering Project Director type of experience – end-to-end project experience of$100m+ package ownership, open on pharma/biotech manufacturing type, start up/ramp up experience important (ops experience receiving facility for a project would be ideal)Work closely with cross-functional teams, including design, equipment, quality, automation, manufacturing and construction, to ensure timely and effective execution.Managing Upstream, Downstream, CIP, clean utilities, facility qualification, and project servicesUnderstanding equipment principles and integrationTake full ownership of the project lifecycle, schedule and budget.Manage and Lead teams for each that will consist of 60–80 people.To be in the field, boots on the ground and be prepared to support the project execution teams  Requirements: Requires extensive experience in process engineering, CQV, or project management, with a strong focus on drug substance biologics projects. Candidates with 10 years of experience and a solid background may also be considered.End to end project experienceExperience in package of equipment of $100 – 200mExperience of managing up to 60 peopleGreenfield project experienceOperational leadership experience alongside project is beneficial. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Project Manager - US, North Carolina - Long Term Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented Project Manager to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. Essential Duties and Responsibilities for this role include, but are not limited to: Project Leadership: Lead the planning, coordination, and execution of facility qualification (EMPQ) projects.Ensure all activities are completed on time, within scope, and budget.Team Coordination: Collaborate with cross-functional teams including Quality Assurance, Engineering, Validation, and Operations to align on project goals, timelines, and deliverables.Ensure that all qualification activities meet GMP, FDA, EMA, and other regulatory standards.Environmental Monitoring: Lead the EMPQ process, including the design and execution of environmental monitoring plans to assess the cleanliness and suitability of facilities for manufacturing.Documentation Management: Ensure that all qualification such as EMPQ activities are thoroughly documented. Review and approve qualification protocols, reports, and other related documentation. Requirements: Requires extensive Equipment experience on Large Scale Biopharmaceutical ProjectsPM experience heavily in bringing facilities togetherClean Room experienceExperience on a large capital projectExperience bring facilities togetherClean Room start up experience If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Clean Utilities Support Engineer - US, Raleigh - Long Term Contract Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Clean Utilities Support Engineer for their Raleigh based location.  Essential Duties and Responsibilities for this role include, but are not limited to, the following: Support the installation of pharmaceutical clean utility systems, including but not limited to WFI, clean steam, and clean gases.Act as the client's agent to review and approve submittals from the Design/Builder for applicable utilities and equipment designs.Participate in constructability reviews with site construction team.Review and comment on applicable detailed design and installation specifications.Drive progress and coordination to ensure schedule, cost and quality targets are metEnsure all clean utility systems are installed according to design specifications, industry standards, and regulatory requirements.Conduct thorough system walkdowns to verify compliance and readiness for mechanical completion.Coordinate with contractors, engineers, and project teams to address issues and maintain project timelines. Desirable Experience: Requires extensive experience in the construction and commissioning of clean utility systems in pharmaceutical or biotech facilities.Strong knowledge of clean utility systems, including water systems (WFI, PW), clean steam, and clean gases.Ability to read and interpret engineering drawings, P&IDs, and technical specifications.Experience with commissioning processes and startup protocols for clean utility systems. If this role is of interest to you, please apply now!#LI-MC1