AccelLAB is looking for a Research Scientist to join our team (hybrid position) If you want to join an SME and a dynamic team, this position is for you! AccelLAB is a preclinical contract research organization dedicated to medical devi[...]
Provides specialized validation knowledge and information, which is directly required to support operations and clients. Completes all protocols related to the validation of equipment, processes, and new products and reviews all finish[...]
Quality Assurance Associate Windsor, NS, Canada Req #1463 Wednesday, March 6, 2024 BIOVECTRA Inc. is a leading bio-science business in Prince Edward Island and Nova Scotia, focused on contract manufacturing and product development of a[...]
executing, coordinating and maintaining qualification activities for Computerized Systems in accordance with regulations and defined Apotex quality standards, procedures and policies.Job Responsibilities Perform system risk and GxP imp[...]
Current Employees apply HERECurrent Contingent Workers apply HERESecondary Language(s) Job Description:The Senior Specialist, Compliance will play a crucial role in ensuring the organization's adherence to regulatory requirements, indu[...]
Quality Assurance Auditor - 12 Month Contract (Days) Job location: Bradford, ON Employment type: Full Time Employment Hours: 40 Hours per week A little about us Hi, we're Aurora Cannabis, and we're so excited to meet you! We're a globa[...]
both locally and regionally, to assure that validation activities and life cycle methodology are incorporated and documented appropriately during and after the project in accordance with company standards and procedures. Key and critic[...]
Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world
Job Summary The Associate Director, External R&D Quality is responsible for developing and implementing Quality Systems to ensure products manufactured, tested and packaged by third party organizations on behalf of Apotex meet the appl[...]
You have prior experience working as a Quality Engineer, preferably in a medical device company based on standards and regulations (ISO 13485, 21 CFR 820, etc.), and have had exposure to providing Quality and Compliance support related[...]