Overview PM Group is a leading International engineering, architecture, project and construction management firm.
With a network of offices in Europe, Asia and the US and a multi-discipline team of over 3,700+ people.
We deliver complex, capital projects in the life sciences, food and beverages, mission critical/ICT, advanced manufacturing, energy and environmental sectors.
Due to our ongoing success securing large-scale projects we are looking to speak with experienced CQV Engineers to support Commissioning, Qualification and Validation of Upstream, Downstream, Syringe line and E-beam systems for our projects in ****.
Projects located throughout Cork region.
Responsibilities Develop and execute CQV documentation Execute FAT/SAT for Upstream Bioreactors, Harvest Vessels and Downstream Chromatography and UF/DF Skids Perform IV, Commission, IQ/OQ and PQ (where applicable) Collaborate with Vendors and internal stakeholders to ensure timely MC and Turnover Ensure compliance with GMP, Data Integrity, regulatory requirements Qualifications Degree in Engineering 3+ years CQV experience in Biopharma or Pharmaceutical projects Hands on CQV experience in one or more of the following:Upstream (Bioreactors, media prep)Downstream (Chromatography, Filtration)Utilities (WFI, Clean Steam, HVAC)CIP Systems Strong understanding of GMP regulations and Validation principles Excellent communication and problem solving skills Preferred Skills Experience in Greenfiels or large-scale CQV Projects.
Ability to manage multiple priorities and work in a fast-paced, regulated environment Strong technical writing and communication skills.