Matthew Gretsch

• Enhanced production efficiency through strategic restructuring resulting in improved output.
• Successfully navigated a legal challenge related to PFAS/PFOAS usage, leading the development of alternative adhesive solutions free from these chemicals.
• Spearheaded the creation and implementation of innovative software facilitating global communication and seamless sharing of methodologies and outcomes.
• Provided real-time floor support, ensuring compliance with GMPs and internal documentation such as SOPs, MBRs, and TMs.
• Conducted timely batch record reviews to support clinical product availability, collaborating closely with operators and technicians to address deficiencies and ensure compliance.
• Ensured compliance with established protocols and regulatory requirements while managing the disposition of raw materials, starting materials, and intermediates.
• Collaborated with Manufacturing teams to investigate and resolve product deviations, actively participating in Quality Assurance (QA) manufacturing deviations and Corrective and Preventive Action (CAPA) processes.
• Ensured accuracy and compliance with regulatory standards for SOPs, Work Instructions (WIs), MBRs, Specifications, and TMs
• Supported QA manufacturing metrics tracking and analysis to drive continuous improvement efforts.
• Cultivated effective working relationships with cross-functional peers and managers to facilitate collaboration and drive quality improvement initiatives.

Led a dynamic research and development team focusing on the creation of cutting-edge medical devices.

• Spearheaded the development of medical devices catering to military and major pharmaceutical clients.
• Pioneered a revolutionary device designed to prevent scar tissue formation post-surgeries.
• Conducted comprehensive research and development initiatives on blood products, including routine analyses of blood plasma, platelets, and fibrinogen.
• Executed meticulous collection and processing of biological specimens in strict accordance with SOPs.
• Ensured strict adherence to laboratory standards, confidentiality protocols, and facilitated effective communication channels.
• Implemented and maintained optimal hygiene standards by applying strict aseptic and sterile techniques to clean surfaces, devices, and specimens.
• Upheld a clean and organized work environment conducive to productivity and safety.
• Trained new team members on SOPs and adhering to good manufacturing practices.
• Safeguard operational integrity by managing administrative tasks such as safety audits, supply management, and coordinating meetings.