Kesia Pires De Oliveira's Email & Phone Number

💼 Past Experience

Kesia Pires De Oliveira has over 10 years of experience in the Pharmaceutical Industry, spanning from Medical Devices and Pharmaceuticals through Cleaning and Validation. She is most recently a Validation Analyst at Biolab Sanus Farmacêutica from February 2006 to February 2007. In this role, she was responsible for the validation of products and services from a range of industries, including Pharmaceuticals, Cleaning and Validation. Kesia also has experience in Project Management and Quality assurance.

🎓 Education

Kesia Pires De Oliveira has an Executive MBA in Leadership and Management from ESMT Berlin. She also holds a Master of Administration in Master of Administration Business Management and Leadership Administration from Saint Paul Escola de Negócios in January 2018 and a Post-Graduate Course in Quality and Productivity from Escola Politécnica da Universidade de São Paulo in January 2006. Kesia Pires De Oliveira specialises in Industrial Pharmacy with a Master’s Degree in Pharmacy from Universidade Estadual de Maringá in January 1999.

💡 Technical & Interpersonal Skills

Validation Analyst at União Química Farmacêutica Nacional from May 2004 to January 2006Kesia Pires De Oliveira is licensed in the United States (USA) to practice a medicine. As a Validation Analyst at União Química Farmacêutica Nacional, she has been authorized to use the national Drugs and Drug Units(DU) and also the Good Laboratory Practice (GLP) dimensions of the Program for medical device validation.As a Validation Analyst, Kesia Pires De Oliveira helps to complete the process of certification and validation of medical devices, paper andSIGNificant efforts focus on quality assurance, control, and safety. She coordinates the work of the CU team and collaborates with other departments within the hospital in order to help provide the highest level of quality and safety for her patients. She also manages and coordinates projects, holds regular team meetings, and participates in stakeholder meetings to discuss the project goals and objectives.Kesia Pires De Oliveira's Professional experience:Kesia Pires De Oliveira is a has a background in Medical Devices, Computer System Validation, Quality Auditing, Technical Recruiting, GMP, Pharmaceutics, MS Project, Validation, Customer Service, Quality System, Inspection, Sop, Quality Assurance, Change Management, Regulatory Affairs, Change Control, 21 CFR Part 11. Project Management, Pharmaceutical Industry, Cleaning Validation. Kesia Pires De Oliveira has 20 years of experience as a project manager and has worked in many different industries. She has experience with project management software such as STRAIGHTLINE and FM. Kesia Pires De Oliveira has also worked with the Pharmaceutical Industry, Cleaning Validation. As a Validation Analyst, Kesia Pires De Oliveira will have a significant impact on the validation process for medical devices. This experience and skillset give her a strong foundation for the Validation Analyst position. interpersonal skills:Kesia Pires De Oliveira has good interpersonal skills and is able to work well with other team members. She is also able to communicate effectively with customers and understand their needs. Kesia Pires De Oliveira is also skilled in quality assurance and has experience working with many different types of products.