Develop, implement and maintain submission delivery plans, content plans, and proactively provide status updates including regulatory risks and mitigation…
The Regulatory Affairs Labelling Associate is responsible for the preparation and on time filing of high quality regulatory drug submissions including Post DINA…
Bachelor’s degree in life science, chemistry, or related field. Participate in the development and implementation of methods, procedures and regulations for the…
4-year degree in a scientific or related discipline and 1+ years' relevant experience for manager level; OR 3+ years' experience for Associate Director level.
Established knowledge of Canadian and U.S. government regulations on ingredient, claims and nutritional labelling: up-to-date and respond to initiatives to…
Minimum 4-year degree in an appropriate & related field (e.g., Life sciences, physical sciences, healthcare, biology, biochemistry, chemistry, chemical…
Minimum B. Sc. in a Chemistry, Pharmacy or Life Science discipline combined with at least five (5) to seven (7) years of hands-on Regulatory Affairs experience…
Regulatory Consultation – Provides technical and regulatory guidance and direction within and outside of the Quality and Regulatory function to enable…
Is required to have a high degree of analytical and technical knowledge and experience, combined with a strong understanding of retail and small business credit…
À titre d'employeur souscrivant au principe de l'égalité d'accès à l'emploi, Conagra Brands considère les postulants qualifiés pour les offres d'emplois sans…
Contribute to the development and implementation of clinical and pre-clinical regulatory strategy for projects in all stages of development (CTA through…
The incumbent will be responsible for working with the Executive Leadership Team (ELT) and senior leadership to create, design and implement the organization’s…
Build a network of trade associations, industry partners, non-profit groups, and others to support policies that will help create/maintain a user-focused online…
Our Quality Assurance System was developed in order to ensure the production of safe and effective products in compliance with the current Good Manufacturing…
The Senior Medical Information Manager is responsible for the proactive planning, development of scientific content to support Medical Affairs, providing…
Manage FA’s internal control process including a) the assessment of changes in controls and remediation plans; b) the quarterly attestation of controls by…
Bachelor’s degree in a science or related field, along with 3 + years of experience. You will also contribute to the development of labelling negotiation…
Undertakes desk-side research to inform strategies, planning, briefing documents, and content development. Research and write: Presentations, briefing notes,…
Partner with local, regional and global operational groups to foster a proactive approach to compliance. Support the qualification and approval of suppliers and…
Estimated: $75,077 -
$95,064 a year
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