Mark Chaumeton

I&C Metrology Engineer - US, North Carolina - 12 Month Initial ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented I&C Metrology 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. What you'll do: Be part of a team of Metrology Specialists, Technicians, and Team Leads Supporting Aseptic and Finish Production areasSupporting calibrations across the site, including Formulation, Filling, QC, Facilities, Finish Production and Component Prep. The calibration program includes on-site and vendor performed calibrations.Supprt for all audit / inspection responsibilitiesDeviation and Change Control responsible (including SPS)Create and maintain department SOPs What you'll need: Bachelor’s degree in Engineering (Instrumentation & Controls, Electrical, Mechanical, or related discipline) or equivalent technical experience.Extensive experience in metrology, calibration, or instrumentation engineering within a GMP-regulated bio-pharmaceutical, medical device, or FDA-regulated manufacturing environment.Experience supporting drug substance manufacturing operations preferred.Strong knowledge of calibration and metrology principles for process, laboratory, and facility instrumentation. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Project Manager - US, North Carolina - Long Term ContractOur 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. What you'll do: Lead the planning, execution, and delivery of capital projects, ensuring alignment with business objectives, schedule, and budget.Develop and manage project scopes, budgets, schedules, and risk assessments, driving accountability across teams.Coordinate with cross-functional stakeholders, including engineering, operations, quality, procurement, and regulatory teams, to ensure seamless project execution.Manage contractor and vendor relationships, overseeing procurement, contract negotiations, and project execution. What you'll need: Extensive experience in capital project management within the pharmaceutical, biotech, or life sciences industry.Proven track record of delivering complex capital projects on time and within budget.Experience managing process equipment, utilities, automation systems, and facility expansions.Strong leadership and communication skills (written and verbal), with the ability to influence, negotiate, and build relationships with stakeholders at all levels. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

QA Validation Engineer - North Carolina, United States - 9-months contractOur client works across regulated sectors to build robust, repeatable compliance and validation practices. They prioritise clear guidance, clean documentation, and controls that fit how teams operate.  What you’ll do: The QA Validation Specialist is responsible for implementing, executing, and assessing quality systems, procedures, and records to support compliant GMP operations.The role works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation teams.Provide hands‑on QA support and oversight to internal teams and suppliers/contractors to ensure compliance with applicable quality standards, regulatory requirements, and industry guidance.Review and approve commissioning, qualification, and validation documentation.Review and approve qualification and validation deviations and discrepancies, supporting investigation and corrective actions.Work collaboratively across site functions to instil a strong quality culture, coaching in the application of GMP principles and the rationale behind them.Author, review, and approve controlled documents for Quality and other GMP functions, including SOPs, specifications, protocols, and reports.Assist in the preparation for, and hosting of, regulatory inspections and audits as required. What you’ll need: Degree in biological, physical or chemical sciences, engineering, or a related field, with  experience in QA within biologics manufacturing. Strong knowledge of risk‑based approaches to qualification and validation in a biotech quality environment.Hands‑on experience with qualification and validation of process equipment, isolators, bioreactors, clean utilities, automation systems, sterile filling, and cleanroom facilities.Solid understanding of relevant regulations and guidelines, including US and EU frameworks (e.g. FDA, EMA), ICH guidance, and industry best practice.Proven track record of working in a fast‑paced team environment, meeting deadlines, and prioritising work across multiple projects.Strong analytical and communication skills, sound judgement, and the ability to work effectively with colleagues and stakeholders.Excellent problem‑solving capability, with experience in root‑cause investigation and CAPA determination. If this roles is of interest to you, apply today!

Building Safety 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 Building Safety Lead for their Raleigh based location.   What you'll do: 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. What you'll need: 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

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 and Controls Engineer - North Carolina, US - 12-month 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 Instrumentation & Controls Engineer for their North Carolina based location.  What you'll do:  Review design drawings and technical documents for accuracy and feasibility.Provide technical expertise to resolve design and implementation challenges.Identify and address technical issues during installation and operation.Develop corrective actions for system discrepancies.Ensure compliance with safety standards in all electrical and instrumentation work.Review instrumentation and equipment submittals.Offer guidance on cabling infrastructure during early design phases. What you'll need:  Extensive experience in electrical and instrumentation systems construction within industrial or engineering projects (pharma, oil & gas, or manufacturing preferred).Hands-on experience reviewing design drawings, specifications, and technical documentation for accuracy and feasibility.Strong technical expertise to resolve design and implementation challenges and troubleshoot issues during installation and operation.Proven ability to develop corrective actions for system discrepancies and ensure compliance with safety regulations.Familiarity with instrumentation and equipment submittals and cabling infrastructure concepts during early design phases.Experience with DeltaV systems.Background supporting large-scale EPCM projects, ideally in pharma, biotech, or regulated manufacturing environments. If this role is of interest to you, please apply now!#LI-MC1

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