We are looking to hire a Quality Assurance Lead for one of our leading global clients in the Pharmaceutical industry in Mississauga.Reporting to the Quality Director, the Quality Assurance Lead will lead Quality discussions to support the successful on-boarding of new clients, products, or processes. Advantages• Competitive salary and company benefits• Bonus structure• Opportunities for professional learning, development, and growth• Working with a fun, entrepreneurial, and supportive teamResponsibilities•Provide Quality leadership to support introduction of new clients and products from development to commercialization; creating and streamlining systems/ processes as required.•Lead Quality discussions to support the successful on-boarding of new clients, products, or processes.•Represent Quality at project meetings, acting as a liaison to other areas of Quality e.g. QC.•Support review of batch records (master or executed) and associated documentation, disposition of batches, deviation investigations for non-commercial production.•Support the quality aspect of planned changes raised to support non- commercial projects, ensuring compliance to procedures and regulations.•Provide final quality approval on documentation generated to support projects. This will include technical reports, validation/verification reports, analytical methods, specifications, risk assessments etc.•Participate actively in Client or Regulatory inspections.•Participate in the creation/coordination of documentation/declarations to support Client registration activities.Qualifications•Bachelor’s degree in science or related field and on the job experience in pharmaceuticals.•Demonstrated understanding of the regulatory framework and current industry quality standards from development to commercialization•Minimum 5 years experience Quality Operations in the pharmaceutical industry. Similar experience in an equivalent industry would be considered. Manufacturing experience is an asset.•Experience in interpreting regulations as it relates to all different stages of drug manufacturing.•Demonstrated ability to develop and lean processes•The ability to influence, problem solve and support other members of your team.•Demonstrated ability to make sound quality risk based decisions in a fast paced environment.SummaryIf this role sounds like a good fit for you, please APPLY ONLINE or submit your resume directly to Mina Khalil at Mina.Khalil@randstad.caThank you for applying for the role. We’ll review your application and connect shortly if you meet all the requirements.Good luck!Randstad Canada is committed to fostering a workforce reflective of all peoples of Canada. As a result, we are committed to developing and implementing strategies to increase the equity, diversity and inclusion within the workplace by examining our internal policies, practices, and systems throughout the entire lifecycle of our workforce, including its recruitment, retention and advancement for all employees. In addition to our deep commitment to respecting human rights, we are dedicated to positive actions to affect change to ensure everyone has full participation in the workforce free from any barriers, systemic or otherwise, especially equity-seeking groups who are usually underrepresented in Canada's workforce, including those who identify as women or non-binary/gender non-conforming; Indigenous or Aboriginal Peoples; persons with disabilities (visible or invisible) and; members of visible minorities, racialized groups and the LGBTQ2+ community.Randstad Canada is committed to creating and maintaining an inclusive and accessible workplace for all its candidates and employees by supporting their accessibility and accommodation needs throughout the employment lifecycle. We ask that all job applications please identify any accommodation requirements by sending an email to firstname.lastname@example.org to ensure their ability to fully participate in the interview process.