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Montréal, QC (undo)
Laporte Experts Conseils
- Provide technical input with respect to Standard Operating Procedures development; review or revise SOP’s as required to assure that all needs are addressed,…
- Review documents and correspondence to ensure they are in compliance with legal procedures and grammatical use ;
- Good bilingualism, oral and written.
$42,000 - $45,000 a year
- Operate and maintain testing equipment and materials used in performance of job.
- Interact with customer to provide guidance as to the operation and maintenance…
- IntelliSyn is looking for motivated pharmaceutical synthetic associate research scientists to help drive our drug discovery programs.
- L’objectif général est que l’étudiant/e apprenne le rôle des affaires médicales.
- Différents projets lui seront assignés dans tous les champs thérapeutiques.
$40,000 - $55,000 a year
- Teach patients, researchers and nurses to follow protocol according to GCP guidelines.
- L’unité de recherche clinique de l'Institut neurologique de Montréal de…
- Attend weekly conference calls and quarterly sales meeting to update product knowledge, share success stories and discuss selling strategies,.
- Complétez l’application en ligne au www.imprespharma.ca pour être considéré.
- TITRE DU POSTE : REPRÉSENTANT PHARMACEUTIQUE.
- Impres Pharma est le chef de file en.
- Reporting to the Manager–Production, you perform all the duties related to the processing and management of biological products.
- Have a good command of French;
- For evaluation of technical compliance activities (Deviations, Change controls, Customer Complaints, CAPAs).
- Fluent in speaking / writing in English;
- (i.e. experience in the design, conduct and management of clinical trials and experience in working with Contract Research Organizations (CROs) or external…
- Team with Product Support Engineers to enable our customers’ success to manage their operations by supporting them remotely through phone, email, or web…
- Review product labels to ensure compliance with Canadian regulations;
- Communicate with external partners to obtain documentation (including GMP evidence,…
- Evaluate from a technical point of view graphical designs provided by customers or according to internal needs;
- Participate in different special projects.
- Other responsibilities are to participate in the planning of assay qualification and validation, to contribute to product stability study design and data…
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