Suraj Chauhan

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

Process Engineer - Victoria, Romania - 6 Month Initial Contract  Our client is the world leader in resin-based separation, purification and extraction technologies, with R&D and manufacturing facilities in several key locations around the world, including the UK, USA, China and Romania. We provide innovative solutions to global pharmaceutical, power, hydrometallurgy, electronics, ground water and Life Sciences industries. Our client’s Life Sciences is a rapidly growing division, they are looking for a Process Engineer to join their team on an initial 6 month contract What you’ll need: Design and optimize chemical processes for manufacturing Ecolab products such as detergents, sanitizers, disinfectants, and associated premixes.Conduct research to develop innovative and improved chemical manufacturing processes.Determine most effective arrangement of unit operations such as mixing, blending, coating, milling, grinding, screening, cooling, shaping, polymerizing, and chemical synthesis. Direct personnel controlling equipment used for such unit operations.Design experiments using statistical analysis to understand dynamics of chemical processes and formulations.Determine process capability through statistical analysis and make recommendations for product and process specifications.Support the Experimental request System application through requirements determination, documentation, and communication with internal and external IT support What you’ll do: Bachelor’s degree in chemical engineeringRequires experience working in an RD&E environmentStrong leadership, teamwork, and interpersonal communication skillsProduct/Process development experienceExperience working in a chemical manufacturing environmentExperimental design knowledge and application experience. If you are interested, please apply now!#LI-SC1

Project Technical Manager - Ireland, Dublin - Permanent 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 a Project Technical 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!Essential Duties and Responsibilities for this role include, but are not limited to, the following: Establish our project’s technical direction for all technical aspects.Develop technical scope for the project and identify resource requirements with project management to deliver the project.Lead and task manage a significant cross-disciplinary SME team and working closely with the SME team to create a seamless transfer of technical responsibilitiesEnsure the full technical scope is aligned with business and project needs.Collaborate with the project execution team including project management, construction management, Automation, IT, Commissioning and Qualification teams to deliver the project scope on time and budget.Support the Operational Readiness team technically where necessary to ensure design is understood and communicated clearly to the Owner.Ensure the technical team keeps to the project scope Desirable Experience: Requires extensive and relevant Capital project technical and execution experience, preferably within the pharmaceutical industry and major capital investmentsExperience of working in a global organisation and you are aware of how "engineering delivery" needs to be adapted to take account of local differences.Experience of working successfully with Design Contractors and Equipment suppliers on major projectsExcellent communication, customer & partner management, enabling and influencing skillsDesign and preferably operational experience in ATEX design and delivery of functional safetyDegree in an Engineering or Science discipline with of experience of project management and/or project delivery If this role is of interest to you, please apply now!#LI-SC1