Maria Angel

WORK HISTORY

EDUCATION

SKILLS

ABOUT MARIA ANGEL

Over 9 years in the medical device field with a proven track record. Broad experience in quality systems, engineering, research & development, new product development, operations, & product marketing.Capable of creating and managing company-wide documentation and records per established policies and procedures. Proactive in problem solving & troubleshooting to find solutions.Skilled in creating and modifying engineering technical documentation, change requests, specifications, bill of material information, etc. Accomplished in complying with company requirements for production schedules and deadlines with a thorough understanding of the documentation process for consumer and medical device products.Have worked independently and as part of a team. Experienced in working in ISO certified manufacturing and FDA regulated medical device industry. Familiar with basic GMPs. Experienced Quality Professional with Quality and Regulatory experience, including Quality Systems, Quality Engineering, Quality Control and Regulatory Compliance, in Class II and Medical Devices.Provided company training on “Engineering Change Control”, “GDP” and “MasterControl System”.Personal qualities: Solid communication and interpersonal skills, able to provide technical support to other departments as required. Dedicated, reliable, loyal, resourceful, adaptable, innovative, detailed oriented, organized, and a good work ethic.Specialties:Packaging and labeling specialist & document control specialist. Extensive experience in defining requirements, material selection, package and label design, product testing in both the medical and consumer electronic fields.