Ability to read and correctly interpret documents such as safety rules, regulations, and specifications. Bachelor’s Degree or College Diploma in science or a…
Bachelor’s degree with 2+ years of related work experience OR Master’s degree in field with 0-2 years of related work experience. This is a remote position.*.
Assister les coordonnateurs de recherche clinique et l'assistant/associé coordonnateur de recherche clinique dans la communication avec le CRA et l'exécution de…
The CRASS will work with the local representatives and other global functions to ensure creation and update of appropriate product labeling content (product…
Provide technical and strategic support to Global R&D for the filing of complex generic drug products to achieve high quality submissions to meet the business…
Benefit programs designed to support our employees and their families, including a comprehensive health & dental benefits package, group RRSP matching program,…
Bachelor’s degree in a scientific discipline with 8+ years of regulatory documentation and operations experience in a pharmaceutical, biotechnology or contract…
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…
Deux (2) ans minimum en affaires réglementaires et/ou les activités d’étiquetage est un atout (médicaments, instruments médicaux, produits de santé naturels,…
Assist in development and maintenance of Standard Operating Procedures, Technical documents, forms, etc. B.Sc. in technical field (Life Sciences, food Science,…
Ability to develop professional networks that will drive business development and regulatory intelligence. Provides teams with direction on regulatory authority…
Management of the Annual Product Quality Report Program: support the APQR program by obtaining and reviewing documents related to the products; confirm product…
Our Quality Assurance System was developed in order to ensure the production of safe and effective products in compliance with the current Good Manufacturing…
Collaborate with business partners to ensure that risks are reviewed for root cause, impact, and recurrence and assure that relevant line function owners put in…
This role will lead the Genomic Medicine pharmaceutical QMS, accountable for the development and implementation of a Cytiva best in class quality program at PNI…
As is typical of a field-based role, employees must be able, with or without an accommodation to: travel by public transportation, automobile, train, or plane;…
This role will lead the Genomic Medicine pharmaceutical QMS, accountable for the development and implementation of a Cytiva best in class quality program at PNI…
Performing first article inspection reports and regular incoming inspections of incoming materials according to established specifications and procedures.
Estimated: $56,291 -
$71,277 a year
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