Logo for Head of Validation and Compliance Consultancy Services

Location:

UKType:

Full-time | On Site | TravelSector:

Life Sciences | Engineering | High-Performance EnvironmentsOverview

Here at T-SQUARED we don''t just design buildings - we

Make Space for Genius .We design, build, validate and maintain highly specialised facilities for scientists and innovators who change the world.We offer an end-to-end solution for the complex, dedicated facilities that high-tech regulated industries need. We make and maintain spaces where our clients do amazing things, from preventing the next global pandemic to cutting-edge research at the speed of light. Their work changes the world, and we make it possible.The Opportunity

T-SQUARED are looking to recruit an experienced Head of Validation and Compliance Consultancy Services to support and develop our team in T-SQUARED Validair. T-SQUARED Validairis a leading provider of contamination control testing, qualification, and GMP compliance services, serving clients across pharmaceuticals, life sciences, advanced manufacturing, and healthcare, across the globe.The successful candidate will be delivering qualification and compliance work across the UK, with occasional overseas assignments. You will assist in the preparation of documentation and on-site validation tasks, developing your expertise in a supportive, hands-on environment as we continue to grow and build our consultancy services team.What You''ll Be Doing

Identify and pursue new business opportunities to drive sales growthLead business development and manage client relationshipsPrepare proposals and presentations tailored to client requirementsDelivery of on-site consultancy servicesDrive improvements in CQV processes and systems to enhance efficiency and ensure complianceManage and train staff as we build our consultancy services teamWhat We Are Looking For

Strong technical background in validation or complianceWorked in or supported qualification projects within cleanrooms or other controlled environmentsExperience in supporting the development or delivery of validation documentation (e.g., URSs, RTMs, VMPs)Familiarity with ISO 14644 standards and cleanroom classification conceptsExposure to authoring or assisting with DQ, IQ, OQ, or PQ protocols-particularly for cleanrooms or contamination control equipmentA basic understanding of GMP principles and awareness of relevant EU GMP guidelinesFamiliarity with cleanroom environments, containment systems, and GMP compliance.Proactive attitude, good organisational skills, and a collaborative mindsetDegree in Engineering, Life Sciences, or a related technical fieldFull UK driving licenceWhy Join T-SQUARED?

Make a Real Impact

- We have been involved in projects that have had a positive societal impact which have supported medical research, pandemic prevention and public health.Career Progression

- Become part of a well-established successful company where your potential to lead is cultivated from the start, and we actively invest in employee development through training, and provide support for professional certifications and charterships.Competitive Package -

We offer a competitive salary and benefits package with opportunities to travel and gain a variety of experiences. We also offer a yearly performance-based bonus.Project Ownership -

Due to our integrated model, you are involved from design right through to maintenance, which means you have direct client contact and have influence across the full lifecycle of projects which makes your work more meaningful and varied.Trusted Name in The Industry - We have been building specialist facilities forover 20 years and are trusted by some of the world''s leading science and healthcare organisations. Our reputation is built on quality, reliability and long-term partnerships.Benefits

31 days holidays (inclusive of public holidays)Annual Bonus scheme linked to Company performanceCompany vehicleLife InsuranceCompany PensionEmployee DiscountsReferral ProgrammePrivate ..... full job details .....