{"id":9325,"date":"2025-12-22T00:30:39","date_gmt":"2025-12-01T11:55:00","guid":{"rendered":"https:\/\/jobtek.eu\/?post_type=job_listing&#038;p=9325"},"modified":"2026-01-07T09:08:08","modified_gmt":"2026-01-07T08:08:08","slug":"pm-group-polska-sp-z-o-o-cqv-engineer-meath-county-meath","status":"expired","type":"job_listing","link":"https:\/\/jobtek.eu\/en\/?post_type=job_listing&p=9325","title":{"rendered":"CQV Engineer"},"content":{"rendered":"<p>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.<\/p>\n<p>&nbsp;<\/p>\n<p>Due to our ongoing success securing large-scale projects\u00a0we now have a requirement for a CQV Engineer to support us on a project in Leinster.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Who Are We<\/strong><\/p>\n<p>PM Group is an employee owned, international project delivery firm with a team of 3,700+ people.\u00a0 We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world&#8217;s leading organisations.\u00a0 We are focused on growing a sustainable business centred around our people, our clients and trade partners.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Responsibilities<\/strong><\/p>\n<ul>\n<li>Lead or support the execution of PPQ protocols for drug substance manufacturing systems.<\/li>\n<li>Develop and manage CQV documentation including:<\/li>\n<li>Collaborate with cross-functional teams including Engineering, QA, and Manufacturing to ensure alignment on qualification strategy.<\/li>\n<li>Ensure compliance with GMP, EU\/FDA regulations, and internal quality standards.<\/li>\n<li>Participate in deviation investigations, cycle development, and performance qualification reporting.<\/li>\n<li>Support vendor FAT\/SAT testing and leverage results for qualification.<\/li>\n<li>Maintain and update the Equipment Validation Master Plan.<\/li>\n<\/ul>\n<p><strong>Qualifications<\/strong><\/p>\n<ul>\n<li>Bachelor\u2019s degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related field.<\/li>\n<li>Minimum 3\u20135 years\u2019 experience in CQV within the pharmaceutical or biotech industry.<\/li>\n<li>Strong understanding of PPQ lifecycle, validation principles, and single-use technologies.<\/li>\n<li>Experience with electronic validation platforms (e.g., Kneat, ValGenesis).<\/li>\n<li>Familiarity with automation systems (e.g., DeltaV, PAS-X) is a plus.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>PM Group is a leading International engineering, architecture, project and construction management firm. 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