Top Benefits
About the role
About The Company
Moderna Biopharma Canada Corporation is a leading biotechnology company dedicated to developing innovative mRNA-based therapeutics and vaccines. Committed to advancing healthcare solutions worldwide, Moderna leverages cutting-edge technology and scientific expertise to address some of the most pressing health challenges. With a focus on quality, safety, and efficacy, the company operates in a highly regulated environment, ensuring that all products meet stringent standards set by health authorities. Moderna’s collaborative culture fosters innovation, continuous learning, and a dedication to improving patient outcomes globally.
About The Role
We are seeking a meticulous and dedicated Quality Assurance Specialist to join Moderna Biopharma Canada Corporation. In this role, you will be instrumental in maintaining the integrity and quality of our pharmaceutical products by reviewing manufacturing processes, monitoring quality systems, and investigating quality issues. Your primary goal will be to ensure compliance with all company policies, Good Manufacturing Practices (GMP), and regulatory requirements, including those mandated by Health Canada. Working closely with production, laboratory, and regulatory teams, you will contribute to continuous improvement initiatives, uphold product safety standards, and support our mission to deliver safe and effective healthcare solutions.
Qualifications
Bachelor's degree in Life Sciences, Pharmacy, Chemistry, Biology, or a related field. Previous experience in quality assurance, pharmaceutical manufacturing, or biotechnology is preferred. Strong understanding of GMP regulations and quality assurance principles. Excellent communication and teamwork skills to collaborate effectively across departments. Proficiency in reviewing documents, conducting investigations, and analyzing quality issues. Strong attention to detail, accuracy, and organizational skills. Ability to work independently and prioritize tasks efficiently. Proficiency in Microsoft Office applications. Knowledge of Health Canada regulations is an asset.
Responsibilities
Review manufacturing documentation, batch records, and validation reports to ensure compliance with regulatory standards. Monitor and audit quality systems and processes to identify areas for improvement. Investigate and document quality deviations, non-conformances, and customer complaints. Collaborate with production and laboratory teams to address quality issues and implement corrective and preventive actions. Participate in internal and external audits, ensuring readiness and compliance. Maintain accurate records of quality activities, investigations, and corrective actions. Assist in the development and review of standard operating procedures (SOPs) and quality policies. Support training initiatives related to quality assurance and compliance standards. Stay updated on industry regulations and best practices to ensure ongoing compliance.
Benefits
Moderna Biopharma Canada Corporation offers competitive compensation packages, including comprehensive health and dental benefits, retirement plans, and paid time off. Employees have access to ongoing professional development opportunities, fostering growth and career advancement. The company promotes a collaborative and inclusive work environment that values diversity and innovation. Additionally, Moderna provides a dynamic workplace with modern facilities and resources designed to support employee well-being and work-life balance.
Equal Opportunity
Moderna Biopharma Canada Corporation is an equal opportunity employer. We are committed to fostering an inclusive environment where all employees and applicants are treated with respect and fairness. We do not discriminate based on race, ethnicity, gender, age, sexual orientation, disability, or any other protected characteristic. We believe diversity enhances our ability to innovate and succeed, and we welcome applicants from all backgrounds to join our team.
Similar Jobs
Top Benefits
About the role
About The Company
Moderna Biopharma Canada Corporation is a leading biotechnology company dedicated to developing innovative mRNA-based therapeutics and vaccines. Committed to advancing healthcare solutions worldwide, Moderna leverages cutting-edge technology and scientific expertise to address some of the most pressing health challenges. With a focus on quality, safety, and efficacy, the company operates in a highly regulated environment, ensuring that all products meet stringent standards set by health authorities. Moderna’s collaborative culture fosters innovation, continuous learning, and a dedication to improving patient outcomes globally.
About The Role
We are seeking a meticulous and dedicated Quality Assurance Specialist to join Moderna Biopharma Canada Corporation. In this role, you will be instrumental in maintaining the integrity and quality of our pharmaceutical products by reviewing manufacturing processes, monitoring quality systems, and investigating quality issues. Your primary goal will be to ensure compliance with all company policies, Good Manufacturing Practices (GMP), and regulatory requirements, including those mandated by Health Canada. Working closely with production, laboratory, and regulatory teams, you will contribute to continuous improvement initiatives, uphold product safety standards, and support our mission to deliver safe and effective healthcare solutions.
Qualifications
Bachelor's degree in Life Sciences, Pharmacy, Chemistry, Biology, or a related field. Previous experience in quality assurance, pharmaceutical manufacturing, or biotechnology is preferred. Strong understanding of GMP regulations and quality assurance principles. Excellent communication and teamwork skills to collaborate effectively across departments. Proficiency in reviewing documents, conducting investigations, and analyzing quality issues. Strong attention to detail, accuracy, and organizational skills. Ability to work independently and prioritize tasks efficiently. Proficiency in Microsoft Office applications. Knowledge of Health Canada regulations is an asset.
Responsibilities
Review manufacturing documentation, batch records, and validation reports to ensure compliance with regulatory standards. Monitor and audit quality systems and processes to identify areas for improvement. Investigate and document quality deviations, non-conformances, and customer complaints. Collaborate with production and laboratory teams to address quality issues and implement corrective and preventive actions. Participate in internal and external audits, ensuring readiness and compliance. Maintain accurate records of quality activities, investigations, and corrective actions. Assist in the development and review of standard operating procedures (SOPs) and quality policies. Support training initiatives related to quality assurance and compliance standards. Stay updated on industry regulations and best practices to ensure ongoing compliance.
Benefits
Moderna Biopharma Canada Corporation offers competitive compensation packages, including comprehensive health and dental benefits, retirement plans, and paid time off. Employees have access to ongoing professional development opportunities, fostering growth and career advancement. The company promotes a collaborative and inclusive work environment that values diversity and innovation. Additionally, Moderna provides a dynamic workplace with modern facilities and resources designed to support employee well-being and work-life balance.
Equal Opportunity
Moderna Biopharma Canada Corporation is an equal opportunity employer. We are committed to fostering an inclusive environment where all employees and applicants are treated with respect and fairness. We do not discriminate based on race, ethnicity, gender, age, sexual orientation, disability, or any other protected characteristic. We believe diversity enhances our ability to innovate and succeed, and we welcome applicants from all backgrounds to join our team.