Pamela Clince
About Pamela Clince
Pamela Clince is a Senior Quality Assurance Specialist at Bristol Myers Squibb in Dublin, Ireland, with a background in Pharmaceutical Sciences from Technological University Dublin.
Current Position at Bristol Myers Squibb
Pamela Clince is a Senior Quality Assurance Specialist at Bristol Myers Squibb, based in Dublin, County Dublin, Ireland. She began her role on June 1, 2021. In this position, Pamela is responsible for implementing and operating Quality Management Systems (QMS) in both upstream and downstream bioprocessing. Additionally, she handles batch record reviews and the review and approval of events and investigations, ensuring the company's compliance with regulatory standards.
Previous Experience at Alexion Pharmaceuticals
Before joining Bristol Myers Squibb, Pamela Clince worked at Alexion Pharmaceuticals, Inc. as a Quality Assurance Specialist. During her one-year tenure from 2020 to 2021 in County Dublin, Ireland, she contributed to the overall quality assurance processes within the organization, gaining valuable experience in the pharmaceutical industry.
Past Role at Therabel
Pamela Clince also worked at Therabel as a Quality Assurance Analyst in 2019. Though her tenure was brief, lasting 3 months in Dublin 4, she played a significant role in supporting the company's quality assurance activities. This experience allowed her to further develop her skills in maintaining high-quality standards in a pharmaceutical environment.
Education in Pharmaceutical Sciences
Pamela Clince holds a Bachelor of Science (Hons) in Pharmaceutical Sciences from the Technological University Dublin. She studied in the program from 2017 to 2021, acquiring a solid educational foundation that supports her professional expertise in quality assurance within the pharmaceutical sector.
Roles and Responsibilities at Bristol Myers Squibb
In her current role at Bristol Myers Squibb, Pamela Clince is involved in various critical activities, such as commercial operations and new product introductions (NPI). Her responsibilities include managing Quality Management Systems (QMS), batch record reviews, and the review and approval of events and investigations. These tasks are essential for maintaining the company's high standards of quality and regulatory compliance.