Carol Sylvester
About Carol Sylvester
Carol Sylvester is a Records Management Specialist, Lead at Bristol Myers Squibb with extensive experience in the pharmaceutical industry.
Current Role at Bristol Myers Squibb
Carol Sylvester is currently serving as a Records Management Specialist, Lead at Bristol Myers Squibb. Located in Devens, Massachusetts, Carol has been in this role since 2018. Her responsibilities include overseeing the records management processes, ensuring compliance with industry regulations, and maintaining meticulous documentation standards.
Professional Experience at Philips
Carol Sylvester worked at Philips as a Documentation Specialist and Document Control Specialist in Andover, Massachusetts from 2017 to 2018 for a period of nine months. In these roles, she was responsible for managing documentation processes, ensuring accuracy, and maintaining compliance with regulatory standards.
Role at QIAGEN
From 2014 to 2017, Carol Sylvester served as Document Control Supervisor at QIAGEN. Her three-year tenure involved overseeing document control processes and ensuring that all documentation met the necessary regulatory and quality standards for the biotechnology sector.
Experience at DuPont Merck Pharmaceuticals
Carol Sylvester amassed substantial experience at DuPont Merck Pharmaceuticals, where she worked as a Technical Writer from 1981 to 2006. Over her 25 years in this role, she specialized in creating detailed technical documents, ensuring compliance with industry regulations, and supporting the company’s communication and documentation efforts.
Educational Background
Carol Sylvester studied at Middlesex Community College. Her education provided her with a solid foundation in the skills required for effective documentation management and technical writing, which she has utilized extensively throughout her career.
Skills in U.S. Title 21 CFR Part 11 Regulation
Carol Sylvester has extensive experience in U.S. Title 21 CFR Part 11 Regulation, a critical regulation that governs electronic records and electronic signatures in the pharmaceutical industry. Her expertise in this area ensures that all electronic documentation processes she oversees are compliant with this regulation.
Proficiency in GMP and Validation
Carol Sylvester possesses strong skills in Validation and Good Manufacturing Practices (GMP). These competencies are essential in the biotechnology and pharmaceutical sectors to ensure product quality and regulatory compliance. Carol’s expertise in these areas contributes significantly to her effectiveness in managing documentation and records.
Career at Bristol Myers Squibb
Carol Sylvester has had an extensive career at Bristol Myers Squibb, beginning with roles such as Technical Writer, Production Planner/Buyer II, and Lead, Records Management from 1997 to 2014. Her long tenure at the company highlights her deep involvement and contributions to the organization's document and records management processes.