David Bruff
About David Bruff
David Bruff is a Senior Validation Engineer at PharmaChem Technologies G.B. Ltd. and a Validation Engineer at Bristol-Myers Squibb, with over 20 years of experience in pharmaceutical projects.
Professional Experience at PharmaChem Technologies G.B. Ltd.
David Bruff is currently a Senior Validation Engineer at PharmaChem Technologies G.B. Ltd. in Freeport, Bahamas. In this role, he focuses on ensuring that projects meet regulatory compliance standards, working closely with various teams including design, project controls, and regulatory affairs. He plays a critical role in delivering projects on time and within budget while ensuring they are fully regulatory compliant.
Role at Bristol-Myers Squibb
As a Validation Engineer at Bristol-Myers Squibb, David Bruff applies his extensive expertise in QA and validation to further the company's pharmaceutical projects. He engages with full project management teams, including CQV, to ensure successful start-ups and brownfield projects. His experience enables him to exceed compliance challenges and deliver projects that meet stringent regulatory requirements.
Over 20 Years of Experience in Pharmaceutical Projects
David Bruff has accumulated over 20 years of experience in the pharmaceutical industry. His work spans various countries and includes multiple projects where he has effectively applied his knowledge of QA and validation. His skill set ensures that projects are not only compliant but also completed according to budgetary and timeline constraints.
Specialization in QA and Validation
David Bruff specializes in quality assurance (QA) and validation within the pharmaceutical industry. His extensive work history showcases his competence in these areas, confirming his ability to deliver compliant and timely project outcomes. His role often includes close collaboration with design teams and full project management teams to meet industry compliance standards.
Track Record of Delivering Compliant Projects
David Bruff has a proven track record of delivering fully regulatory compliant projects on time and within budget. His ability to meet and exceed the stringent compliance challenges in the pharmaceutical industry makes him a valuable asset to his employers. His experience in working closely with different teams ensures that all aspects of a project are well-managed and compliant.