Farhan Younas

CQV/Qualification Engineer - Dortmund, Germany - 2-3 Months Initial ContractThis innovative organisation is a global leader in the development and manufacturing of high-quality sterile injectable products, offering solutions tailored to meet the needs of both clinical and commercial markets. With a strong focus on cutting-edge technologies, they are actively driving advancements in drug substance manufacturing. Notably, their current project in Germany is centred around implementing single-use technology, which enhances efficiency and flexibility in the production process. What you'll do: Develop and execute qualification documents including URS, risk assessments, IQ/OQ protocols, reports, and supporting documentation.Collaborate with stakeholders to ensure timely review and approval of documentation.Report progress, manage timelines, and ensure alignment with project milestones. What you'll need: Extensive experience in CQV/qualification engineering within the biopharmaceutical industry.Proven track record qualifying equipment such as bioreactors, ultra-filtration, chromatography, and related systems.Strong knowledge of GMP, regulatory requirements, and risk management principles.Fluent German speaker (mandatory). If this role is of interest to you, please apply now!#LI-FY1

Electrical Engineer - Ireland, South Dublin - 12 Months Initial ContractAre you local to Dublin and looking for your next contract assignment? Our client, a leading pharmaceutical organisation, are recruiting for an Electrical Engineer to join their newly assembled team and help contribute towards the development of their next core projects.   What you'll do: Champion and lead the ongoing compliance and adherence to all electrical work.Review Capital Project Appropriation submission requests for all electrical work on upgrades.associated with new projects.Implement and maintain the site's Electrical standards. What you'll need: A degree in Electrical Engineering is essential.Extensive experience in a similar role in a GMP-regulated manufacturing environment plus exposure to Electrical installations within an ATEX environment.Experienced in similar roles within the Pharmaceutical/Chemical industry, the candidate will have a proven track record of consistent high performance and delivery in a complex, global, and matrixed environment.Deep understanding of GMP and the Quality standards required in the API Manufacturing sector. If this role is of interest to you, please apply now! #LI-FY1

Construction Safety Lead - Denmark, Copenhagen - 12 Month ContractOur client, a global pharmaceutical company, are looking for a Construction Safety Lead 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: Oversee all aspects of the day to day EHS management of the project.Encourage and develop conduct with respect to safety and be a visible and energetic presence on the site.Determine minimum safety training requirements for construction personnelProvide EHS Training and Leadership by example.  What you'll need: Experience working within the Life Science industry.Experience working within large capital projects.Experience working in all phases of a capital project, ideally from Design to Handover. If you would like to apply or find out more, get in touch now!#LI-FY1

Facility & Maintenance Manager - Italy, Paterno' - Permanent ContractAre you local to Paterno and looking for your next contract assignment? Our client, a leading pharmaceutical organisation, are recruiting for a Facility & Maintenance Manager to join their newly assembled team and help contribute towards the development of their next core projects.   What you'll do: Lead the maintenance strategy across production equipment, cleanrooms, HVAC systems, and site infrastructureDevelop and implement preventive and predictive maintenance plans, aligned with GMP and EHS standardsOwn and optimise our CMMS system, ensuring accurate asset tracking, work order management, and performance reportingManage critical utilities (WFI, HVAC, compressed air, purified water, etc.) to ensure up time and regulatory compliance What you'll need: Degree in Mechanical, Electrical, or Industrial Engineering (or equivalent experience)Requires extensive experience in a GMP-regulated manufacturing environment, ideally within API or pharmaceutical productionStrong working knowledge of CMMS platforms, technical documentation, and regulatory standardsProven leadership in managing multi-disciplinary teams and external contractors If this role is of interest to you, please apply now! #LI-FY1

Automation Engineer - Shanghai, China - Permanent ContractDo you want to be involved with exciting pharmaceutical projects? Our client specialises in data-intelligence, data-driven technology solutions for businesses, and process optimisation, Within the life sciences sector. They are looking to add to their team and require an Automation Engineer.What you'll do: Design, develop, and commission automation systems using Siemens PLCs (S7, TIA Portal) and SCADA platforms.Collaborate with cross-functional teams to implement Electronic Batch Records (EBR) in alignment with GMP and regulatory requirements.Lead the integration and configuration of OSIsoft PI Historian for real-time data acquisition and analysis.Support the deployment of new automation technologies and digital transformation initiatives across the facility.Troubleshoot and optimize automation systems to ensure high availability and performance. What you'll need: Bachelor’s degree in engineering, Automation, or related field.Requires extensive experience in automation engineering within a GMP-regulated manufacturing environment.Proven expertise with Siemens automation platforms (e.g., S7-300/400/1500, TIA Portal, WinCC).Hands-on experience with EBR systems (e.g., Werum PAS-X, Emerson Syncade, or similar).Strong knowledge of OSIsoft PI System (installation, configuration, asset framework).Familiarity with batch processing, ISA-88, and ISA-95 standards. If this role is of interest, apply now! #LI-FY1

Construction Manager - Denmark, Copenhagen - 12 Months Initial ContractOur client, a global pharmaceutical company, are looking for a Construction 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: Oversee’ss all aspects of day to day construction on the project.Deliver a best-in-class facility with respect to the construction scope in line with industry best practices, within budget and schedule without compromising safety.Initiate and maintain an open relationship with the DD team and the wider NN team to ensure successful project delivery.Encourage conduct with respect to safety through action and leadership. What you'll need: Experience working within the Life Science industry.Experience working within large capital projects.Experience working in all phases of a capital project, ideally from Design to Handover. If you would like to apply or find out more, get in touch now!#LI-FY1