qa and ra consultant - manufacturers - 13485 - ivdd - ivdr - mdd - mdr - 510 k - fda - edinburgh - glasgow - stirling@ CHIARA Regulatory Consultancy Services Ltd
Edinburgh, Edinburgh, United Kingdom
Lesley Paice
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英国格拉斯哥大学
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FlashIntel GPTLesley Paice is a highly experienced regulatory and quality professional with 29.8 years of work experience. She has a strong background in quality system, oncology, regulatory affairs, validation, and regulatory requirements. Lesley has worked in various roles, including Managing Director and Quality and Regulatory Affairs Manager. She has a proven track record of gaining regulatory approvals for new IVD and medical device products in different markets. Lesley is skilled in implementing quality and regulatory improvements to ensure the maintenance of quality systems and product certification. She is also skilled in developing innovative solutions to ensure regulatory and quality compliance.
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About
Sixteen years experience in RA / QA and six years in R&D in the medical device industry. I am a highly motivated and enthusiastic regulatory and quality professional with strong project management, communication and people management skills. I have a demonstrated track record in gaining regulatory approvals for new IVD and medical device products in a wide range of different markets. Experienced in identifying and implementing quality and regulatory improvements to ensure maintenance of quality system and product certification. I have experience in developing innovative and pragmatic solutions to ensure regulatory and quality compliance with minimal impact to the business.
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qa and ra consultant - manufacturers - 13485 - ivdd - ivdr - mdd - mdr - 510 k - fda - edinburgh - glasgow - stirling
Managing Director
Medical Equipment Manufacturing
Lesley Paice's Professional Milestones
- Managing Director (2016-01-01~): Driving strategic initiatives, expanding market share, and creating a vibrant market presence through personalized leadership.
- Regional Director Qa/ra Europe And Middle East (2009-01-01~2011-01-01): Expanding quality assurance processes across Europe and Middle East regions.
Education
Biochemistry
1990-1994Skill
Quality System
Oncology
Regulatory Affairs
Validation
Regulatory Requirements
Iso 13485
Quality Assurance
Medical Devices
Iso 14971
Quality Control
Gmp
Clinical Trials
Sop
Capa
Fda
Design Control
Change Control
Regulatory Submissions
U.s. Food And Drug Administration
Certification
Other Named Lesley Paice
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Lesley Paice works for CHIARA Regulatory Consultancy Services Ltd
Lesley Paice's role in CHIARA Regulatory Consultancy Services Ltd is qa and ra consultant - manufacturers - 13485 - ivdd - ivdr - mdd - mdr - 510 k - fda - edinburgh - glasgow - stirling
Lesley Paice works in the industry of Medical Equipment Manufacturing
Lesley Paice's latest job experience is qa and ra consultant - manufacturers - 13485 - ivdd - ivdr - mdd - mdr - 510 k - fda - edinburgh - glasgow - stirling at CHIARA Regulatory Consultancy Services Ltd
Lesley Paice's latest education in 英国格拉斯哥大学
