Through stringent contamination control programs and adherence to cGMP protocols, GDI ensures the integrity of your production environment.
By minimizing risk of product contamination and eliminating cross-contamination, we safeguard not only the quality of your products but also comply with regulatory standards, making GDI your trusted partner in maintaining the highest standards of cleanliness and safety.
Customized cleaning protocols for maintaining sterile environments including:
Thorough cleaning solutions to eliminate construction residues and contaminants, ensuring your cleanroom meets operational standards before use.
Rigorous contamination and particle control measures to meet cGMP protocols.
Safe movement and disposal of non-hazardous and biological waste
Advanced sterilization techniques for critical environments.
Streamlined logistics services ensuring that your operations run smoothly.
Inspection of safety devices, eye wash and shower stations, spill kits, fire extinguishers, incubators and CTUs (controlled temperature units).
Head of GMP Vertical
Vice President of Operations -
North America, Life Sciences
Division
Sr Director of Business Development/GMP SME – North America, Life Sciences Division
Compliance Director – North America, Life Sciences Division
Senior Vice President,
Northwest
Vice President of Risk & Safety
Vice President of Quality Assurance Business Services Group - US
Lab Operations SME & Business Development Manager
Ted Kyranos is a distinguished leader in Life Sciences operations, bringing a wealth of expertise to his role as Vice President of Operations, Life Sciences at GDI. With a robust background in GMP cleaning and disinfection, health and safety device inspections, contract administration, vendor management, people management, and regulatory oversight, Ted’s career is a testament to his unwavering commitment to excellence.
Ted’s extensive experience and technical proficiency in GMP and Contamination Cleaning have positioned him as a key player in driving GDI’s ambitious growth in the Life Sciences sector. His leadership and deep industry knowledge are instrumental in maintaining the highest standards of operational excellence.
Mabia Tavares is a master of excellence in the field of Good Manufacturing Practices (GMP) and contamination control. As a distinguished GxP Subject Matter Expert (SME) with a profound background in cGxP facilities services management, compliance, and training, her career is a testament to unwavering dedication and expertise. With extensive experience across the Biopharmaceutical and Semiconductor industries, Mabia has honed her skills in the crucial areas of GMP, Client and Contract Management, Life Science contamination control programs, and ensuring GMP/ISO compliance. Her ability to manage multidisciplinary project teams and her proficiency in languages, including Portuguese and Spanish, further exemplify her versatile skill set.
Experienced Life Sciences Compliance/quality professional with an emphasis on medical device, biopharmaceutical, and Semiconductor manufacturing industries. Solution-driven with expertise in aseptic manufacture, critical process improvement, deviation closure and CAPA implementation with expertise in the following areas: Contamination Control for sterile Manufacturing, Controlled Environments. Annex 1, (ISO-1644, EN ISO 14698/EN ISO 17141, ISO 17025, IEST RP CC001/CC0012, ANSI/AAMI ISO11737), Medical Devices (ISO 9001, ISO 13485, ISO 14971), Pharmaceuticals (21CFR Part 210, 211), GLP (21CFR, Part 58).
Yogi Kale is a seasoned professional with 33 years of rich, intercontinental experience in facilities management and the hospitality sector, currently serving as the Senior Vice President at GDI Integrated Facility Services. With a deep-rooted passion for clean-tech innovation and operational excellence, Yogi leads the Western Region in organic growth, fiscal performance, customer retention, and enhancing employee experiences. His expertise extends across Integrated Facility Management (IFM), Environmental, Social, and Governance (ESG), Good Manufacturing Practice (GMP), and other compliance standards.
Yogi has played a pivotal role in elevating GMP cleaning services to meet stringent regulatory standards, crucial for industries such as pharmaceuticals, food, and semiconductor manufacturing. He has managed datacenter cleaning protocols and the development of cleaning standards compliant with FDA regulations. A strong advocate for continuous improvement and ethical integrity, Yogi drives business growth and client satisfaction through innovative technology platforms, strategic planning, and fostering multicultural relationships. Under his leadership, clients experience elevated standards of cleanliness and sustainability, ensuring GDI remains at the forefront of the facility services industry.
Jonathan Sauze has 16 years of combined hands-on and managerial experience in Health, Safety, Security, Environmental, Quality, and Risk Management in manufacturing, transportation, and facility services. Jonathan is a Certified Safety Professional (CSP), and Lead Auditor for ISO 45001:2018 and ISO 14001:2015. Areas of expertise include Environmental & Safety Management, Program/Project Management, Inspections & Auditing, OSHA/ISO Standards & Compliance, Root Cause Analysis, Behavior-Based Safety, Safety Management Systems, Continuous Improvement, Risk Assessment, Hazardous Waste Management, Partnership Management, Strategy Planning, and claim Management. As VP of Risk & Safety for GDI US, Jonathan leads the development and execution of H&S initiatives in partnership with the field operation team to promote a workplace safety culture. This includes developing, implementing, and coordinating H&S programs and policies to ensure corporate goals attainment as well as compliance with all applicable regulations.
Mike Cadotte has 30 years of experience with GDI and is a systems process professional who developed, installed, and has maintained GDI’s various quality certifications including ISO 9001, ISO 14001, and CIMS standards. Mike’s dedication to process control and total quality management has been a decades long pursuit at GDI. Mike oversees all quality programs for the US and leads GDI’s global ESG effort as well. Mike has developed GDI’s subject matter expert team initiatives that includes the GxP-Life Sciences Subject Matter Expert Team with the direct intent to not only maintain solid process, procedure, and quality service delivery controls in that vertical but continue to build, learn, and grow GDI’s understanding of GxP-Life Sciences so as to continually maintain the highest level of excellence in the industry.
Under our team’s expertise, GDI Integrated Facility Services transcends the ordinary, offering unparalleled GMP cleaning and contamination control services.
Our innovative approach to problem-solving, dedication to continuous improvement, and proven leadership in executing complex projects make GDI a valuable asset to any organization seeking GMP compliance.
Choosing GDI means partnering with a team that is not just proficient in GMP standards but is also committed to elevating the standards of cleanliness and compliance in your facilities.
Trust in GDI to guide your operations to excellence in GMP compliance and contamination control.
Our technicians are trained in cGMP protocols, utilizing the latest in cleaning technology and practices to maintain your production environment’s integrity.
Yes, GDI’s services are tailored to meet the specific requirements of various industries, including pharmaceuticals, biotechnology, medical devices, and semiconductor manufacturing.
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