Jack Steadman

HVAC Lead - Denmark, Copenhagen - 12 Months Initial ContractOur client, a global pharmaceutical company, are looking for a HVAC 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: Work alongside the EPCM/V and provide direction on areas that can be exploited. The site is huge and they need to help improve the delivery of the EPCM/VIdentifying opportunities to improve scheduleEnsure EPCM/V progress reporting is accurate and if not ensure this is resolvedEnsuring EPCM/V are allocating enough bodies into right areas to achieve required progress What you'll need: A strong background on previous project work in the Pharmaceutical IndustryRobust personalities who can strongly and confidently manage the EPCM/VStrong HVAC experience. If you would like to apply or find out more, get in touch now!#LI-JS5

Project Manager - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Project Manager for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Manage the brand’s book of workDrive scenario planning for projects (with a focus on device, packaging & DP)Develop detailed project timelines, resource plans, and chartersCreate and manage project budgets What you’ll need: BA/BS in a life science, engineering or other technical discipline ExperienceA demonstrated track-record of success, accomplishments & delivering resultsExtensive project management experience within the pharmaceutical/biotech industryExperience with Chemistry, Manufacturing & Controls (CMC) and Packaging, Devices and Artwork desirableExperience with Chemistry, Manufacturing & Controls (CMC) and Packaging, Devices and Artwork desirable If this role is of interest, please apply now!#LI-JS5

MS&T Process Engineer - Ireland, Dublin - 11 Months Initial Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a MS&T Process Engineer. Essential Duties and Responsibilities for this role include, but are not limited to, the following: Demonstrated leadership and change management skills with a continuous improvement focus.Proven track record of delivering high performance through development and coaching of a team.Evidence of continuous professional development.Strong collaboration to promote knowledge sharing and implementation of best practices across the site.SME in upstream/downstream processing and process control strategies. Working knowledge of analytics.Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment. Desirable Experience: Relevant technical qualification(s) in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualificationExperience leading technical related projects.Experience with upstream cell culture and/or downstream purification of biological molecules.Experience in preparing for and presenting in front of regulatory audits as SME.Experience with technology transfer, regulatory filing and commercial drug substance manufacturing of biologics is a plus. If this role is of interest to you, please apply now!#LI-JS5

Quality Specialist - Ireland, Waterford - 11 Months Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Quality Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: Includes participating in and supporting the site PVC (Process Validation Committee), WVC (Water Validation Committee), CVG (Cleaning Validation Group),) and Equipment Qualification Validation Committee (EQVC).Approval of all validation documentation and ensuring compliance to MMD policies, procedures and guidelines. Ensures that validation status is maintained following changes/modifications.Supports the implementation of site or capital projects by defining validation requirements and providing technical assistance and support as a member of the project teams.Develops Validation Summary Reports and assist in developing overall Quality plans for major projects.Works with other areas in MMD and industry to predict future trends in validation and to determine best practice. Desirable Experience: The incumbent must be assertive with excellent communication skillsExperience with QMS SystemsQuality Assurance/Quality SpecialistStrong Communication skills both written and oral including persuading others If this role is of interest to you, please apply now!#LI-JS5