Maree Anderson
About Maree Anderson
Maree Anderson is a QARA PMS Specialist at Teleflex Incorporated in Athlone, Leinster, Ireland, with a background in biotechnology, beauty therapy, and quality assurance.
Title at Teleflex Incorporated
Maree Anderson holds the position of QARA PMS Specialist at Teleflex Incorporated. Based in Athlone, Leinster, Ireland, she has been serving in this role for over five years. QARA PMS Specialists are responsible for overseeing quality assurance and regulatory affairs related to post-market surveillance, ensuring compliance with industry standards and regulations.
Career at Athlone Laboratories
Maree Anderson worked at Athlone Laboratories as a Documentation Controller from 2016 to 2018. During her two-year tenure in Ballymurray, Co. Roscommon, she managed and controlled documentation processes. This role involved maintaining accurate records and ensuring compliance with regulatory requirements, which are crucial for quality assurance in pharmaceutical production.
Experience as Quality Analyst at Europharma Concepts
From 2010 to 2016, Maree Anderson was employed as a Quality Analyst at Europharma Concepts. Over these six years, she focused on quality assurance and control, playing a key role in maintaining high standards in pharmaceutical production. Her work ensured that products met all necessary regulatory and safety requirements.
Education in Regulatory Affairs and Biotechnology
Maree Anderson has a robust educational background, reflecting her diverse expertise. She earned a BSc (Hons) in Biotechnology from Athlone Institute of Technology (2007-2010). Later, she pursued a Level 8 Certificate in Medical Technology Regulatory Affairs and Quality Programme from IT Sligo (2019-2020). This educational experience has equipped her with in-depth knowledge in both biotechnology and regulatory affairs. Additionally, she has a Certificate in Beauty Therapy from Haven Beauty and Training (2014-2015).
Career Transition and Diverse Expertise
Maree Anderson transitioned from a career in beauty therapy to regulatory affairs and quality management in the medical technology industry. Her experience spans different fields including biotechnology, beauty therapy, documentation control, and quality analysis. This diverse background provides her with a unique perspective on quality assurance and regulatory compliance, making her a versatile professional in her current role.