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Matteo Scipioni

@matteoscipioni

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Experienced mechanical engineer specializing in pharmaceutical production and QA.

Italy

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What I'm looking for

I am looking for a role in a dynamic company that fosters growth and teamwork.

I am a dedicated mechanical engineer with a strong background in pharmaceutical production, quality assurance, and manufacturing technology. With a First Class Honours Masters in Mechanical Engineering, I have accumulated four years of professional experience in international companies, where I have honed my skills in production management and staff leadership. My expertise extends to data integrity, compliance, and process optimization, making me a valuable asset in any engineering team.

Throughout my career, I have successfully contributed to significant international projects that have led to cost reductions and enhanced production efficiency. My roles at Takeda and GSK have provided me with diverse opportunities to implement corrective actions, conduct gap analyses, and ensure compliance with GMP standards. I thrive in collaborative environments and am passionate about continuous improvement and innovation in engineering practices.

I am now seeking a position in a progressive company that values growth and teamwork. I am eager to further develop my skills in product development, manufacturing, and management, and I look forward to contributing to a team that excels in delivering high-quality results.

Experience

Work history, roles, and key accomplishments

Current

Quality System, Data Integrity Specialist

Current

Takeda

Jun 2020 - Present (5 years 1 month)

Led manufacturing projects to ensure data integrity requirements were met. Served as a team member for the MES (PAS-X) project and provided training for Data Integrity SOPs.

Data Integrity SOP Development Gap Analysis Project Management

Quality Operations Coordinator

Takeda

Mar 2016 - Present (9 years 4 months)

Conducted batch record reviews for GDP and compliance, and monitored floor activities to ensure high operating efficiency and GMP levels. Identified improvement opportunities and implemented action plans for CAPA to increase GMP compliance.

GDP Batch Record Review CAPA Quality Assurance

Process Expert

GSK – Glaxo Smith Kline

Aug 2015 - Present (9 years 11 months)

Provided front-line support to Manufacturing, collaborating with shift teams and supporting process validation and re-validations. Contributed to product and process-related investigations, including deviations and complaints.

Data Analysis Root Cause Analysis

Manufacturing Technology Investigator

Bristol-Myers Squibb

Oct 2014 - Present (10 years 9 months)

Conducted investigations on production deviations and market complaints, demonstrating knowledge of oral packaging and sterile production lines. Participated in green belt and robustness projects, and performed batch record reviews.

SAP LIMS Trackwise Batch Record Review

Management

IsoBlok.eu Snc

Jul 2012 - Present (13 years)

Monitored, planned, and organized all activities from administration to production, including ordering goods and materials. Managed staff, provided general supervision, and handled customer service and problem resolution.

Production Management Logistics Customer Service Supply Chain Management

Education

Degrees, certifications, and relevant coursework

University of L'Aquila

Master of Science, Mechanical Engineering

Grade: First Class Honours (110/110)

Achieved First Class Honours (final mark 110/110) in Mechanical Engineering. This postgraduate program provided advanced knowledge and skills in mechanical engineering principles.

University of L'Aquila

Bachelor's Degree, Mechanical Engineering

Grade: First Class Honours

Completed a Bachelor's Degree in Mechanical Engineering, earning First Class Honours. This foundational program covered core concepts and principles of mechanical engineering.