Suraj Chauhan

Work Package Owner - UK/Remote- 12 Month ContractHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of a Work Package Owner to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do: Assists project manager or line manager within project leadership in planning and delivering defined work scope on a project to meet agreed schedule and budget.Coordinates with all projects related members on day-to-day progress of work activities to ensure timely completion of a project.Acts as a package lead or area lead within a project.Prepares regular project reports and presentations for key stakeholders. What you'll need: Take lead of the equipment facility fit out for our Singapore siteSupporting the detailed Design activities for DS process equipment. (Bioreactors / Chromatography Skids)The candidate should have experience of DSP in a life sciences context.The role is execution focused (as with all WPOs) rather than been a lab ‘subject matter expert’ the person needs to coordinate and drive the package forwards If this role is of interest to you, please apply now! #LI-SC1

Manufacturing/Validation Specialist - Netherlands, Arnhem - 6 Months Initial ContractHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of a Manufacturing/Validation Specialist to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll need: Reviewing and approving validation tests in TLS (Tulip Validation)Drafting implementation protocols, executing change controls, and updating work processes for shopfloor implementationHands-on mentality, proactive approach, and flexible attitude to implement the EBR process as quickly as possibleAssessing implementation and validation against current GxP guidelines Desirable Experience: Change controls – Independently executingChange ControlsDocumentation updateKnowledge of current GxP regulationsFlexibility and a hands-on mindsetStakeholder / Vendor Management If this role is of interest to you, please apply now! #LI-SC1

QMS Specialist - Ireland, Cork - 12 Month ContractAre you based in Cork, looking for your next long-term contract? We are recruiting for a superb opportunity on behalf of our client, an international contract development and manufacturing organisation who help bring new and off-patent drugs to market. With a track record of over 60 years delivering advanced technologies, this organisation flies in the face of difficulty, giving their customers a service and product that cannot be found elsewhere.This role is based in Cork and is advertised on a contractual basis of 12 months.What you'll do: Responsible for ensuring that the quality systems in used are in compliance with cGMP and the associated regulatory requirementsAct as site lead for nominated quality systems (e.g. EDMS, Deviations, CAPA, Quality Management etc), responsible for trending review and resolution of issuesEnsure that quality issues are identified, addressed and resolved in a timely mannerProvide detailed knowledge of quality systems in place and ensure that root cause is identified and corrective actions as appropriate are completed What you'll need: Motivated to be an inspiring member of a high performing team.Excellent interpersonal skills: communication, decision making, people influencing skills.Ability to interact with multiple stakeholders.Excellent knowledge of relevant Quality and Compliance Guidelines (cGMP, Auditing, Quality Management Systems, Quality Agreements,Regulatory Affairs, Training) and respective regulations. If this role is of interest, please apply now!#LI-SC1

Project Manager - Netherlands - 6-monthsHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the world? If yes, then this is the assignment for you! Our client is currently seeking the skills of a Project Manager to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do:  Support project managers in planning and delivering defined work scopes on time and within budget.Coordinate daily activities with project team members to ensure timely completion.Act as package or area lead within projects.Prepare regular reports and presentations for stakeholders.Track actions and mitigation activities in the project risk management plan.Organize and lead effective work sessions (e.g., PDR meetings).Ensure compliance with project management processes (CPDP), engineering standards, and safety regulations.Assist in resource planning and cost optimization.Contribute to sourcing strategy, vendor negotiations, and integration of multiple suppliers.Coordinate permitting of planned assets and manage supplier performance.Participate in Mechanical Completion walkdowns and close punch items.Support commissioning, qualification, and system start-up activities.Manage lifecycle documentation, including as-built drawings and O&M packages.Oversee FAT and SAT events, documentation, and deviation closure. What you'll need: Experience as a Project Manager, ideally within pharmaceutical environments.Proven background in GMP compliance and clean room projects.Strong stakeholder and vendor management skills.Ability to work on-site as required. If this role interest you, apply today! #LI-SC1

C&Q Lead - Puerto Rico, Remote Working - 12 Month Contract This is a fantastic opportunity for a C&Q Lead to join our major, global pharmaceutical client on their latest new-build project based in Puerto Rico, this is a large-scale greenfield capital project and investing more than $1bn. What you'll do: Lead the development of an effective safety programs from procedure development to execution in the field during project C&Q.Ensure the CQ team abide by all project safety requirements and procedures pertaining to their role and supplement the safety program to cover CQ specific activities as applicable; serve as a positive model to others in this regard.Develop and implement comprehensive C&Q strategies for major capital projects, including parallel commissioning of multiple production facilities and support buildings in a GMP and process safety regulated environment.Manage the development of CQ strategies and execution plans, schedule, and budget to ensure timely and cost-effective delivery. What you'll need: Large C&Q project experience, strong OSD experience, C&Q strategy delivery and a proven track record of managing large-scale programs, full lifecycle – design to handover, ASTM E2500.Experience in budget and scheduling.Experience in managing large project teams If this role is of interest, please apply now! #LI-SC1

C&Q Lead - US, Remote Working - 12 Month Contract Be part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in US, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a C&Q Lead to join the team and help deliver this world-class program. What you'll do: Lead the development of an effective safety programs from procedure development to execution in the field during project C&Q.Ensure the CQ team abide by all project safety requirements and procedures pertaining to their role and supplement the safety program to coverCQ specific activities as applicable; serve as a positive model to others in this regard.Develop and implement comprehensive C&Q strategies for major capital projects, including parallel commissioning of multiple production facilities and support buildings in a GMP and process safety regulated environment.Manage the development of CQ strategies and execution plans, schedule, and budget to ensure timely and cost-effective delivery. What you'll need: Large C&Q project experience, strong MABS/biologics experience, C&Q strategy delivery and a proven track record of managing large-scale programs, full lifecycle – design to handover, ASTM E2500.Experience in managing budget and scheduling. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-SC1

Automation Project Manager - Prague, Czechia - 6 Month ContractOur client, a global pharmaceutical company, are looking for an Automation Project Manager to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems. What you'll do: Lead DeltaV modifications required w/i BRF project and their implementation through design, coding, commissioning and qualification.Drive project planning, scheduling and tracking with internal clients and with contractors.Act as the primary point of contact for internal stakeholders and external vendors.Facilitate interface agreements and align deliverables across contractors and departments Financial & Quality OversightOversee the preparation and approval of project documentation including PQMP, FAT/SAT protocols, and validation reports What you'll need: Bachelor’s or Master’s degree in Engineering, Automation, or related field.Requires extensive experience in project management within PROCESS AUTOMATION, preferably with DeltaV systems.Strong knowledge of GMP, GAMP5, and automation lifecycle documentation.Proficiency in project management tools and methodologiesVery good communication, negotiation, and leadership skills.Fluent English is a must, Czech language is a benefit, not a condition If you would like to apply or find out more, get in touch now!#LI-SC1

Automation Specialist - UK, Cheshire - 9 Months Initial Contract How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of an Automation Specialist (Visual Inspection) to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do: URS’s GEP and GMP Automation / AVI part onlySetting and agreeing the Automation Design Philosophy, in alignment with the Automation and AVI strategies, technical standards and guidelines and local realties and expectations.Supporting the Design Contractor(s) and Vendor(s) with translation of the agreed Automation Design Philosophy and User Requirements into Engineering deliverables.Provide design assurance overview and technical feedback throughout the project to ensure ongoing technical alignment and identification of value engineering opportunitiesEngage in the execution of design reviews What you'll need: Automation background – CCW ConnectedComponents Workbench (Rockwell) (Part code)Vision inspectionProcess ImprovementProcess Control (Dye / Execution projects)Test ConceptCye manufacering processPart validation If this role is of interest to you, please apply now!#LI-SC1

Packaging SME - UK, Manchester - 12 Month ContractHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of a Packaging SME to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do: Front End study support including technology selection capacity calculations and preliminary equipment sizing.Provide subject matter expertise for URS development and approval of GMP equipment/systems.Ensure appropriate engineering standards are incorporated into user requirements.Lead process risk assessments in order to establish and deliver safe process operations and meet drug product quality requirements.Support procurement’s strategic supplier management efforts, establish qualified suppliers and bid evaluations. What you'll need: Packaging experience – Blister linesURS – Review / ApproveStakeholder / Vendor management If this role is of interest to you, please apply now!#LI-SC1