🕐 Posted 6d ago

Manufacturing Operator - SPECTRAFORCE

SPECTRAFORCE

LavalFull-timeMid LevelOn-site

Job Description

French Version:

Titre : Opérateur de fabrication

Durée : 6 mois

Lieu : Saint-Laurent, QC

Taux horaire: $28.96/hr


Remarque : Doit ĂȘtre parfaitement bilingue en français et les candidats doivent ĂȘtre disponibles pour travailler sur n’importe quel quart de travail, en comprenant que les quarts peuvent changer rĂ©guliĂšrement.


Résumé du poste :

ConformĂ©ment aux politiques, directives, procĂ©dures, dossiers de fabrication et aux Bonnes Pratiques de Fabrication (BPF/GMP) Ă©tablis, ainsi qu’aux mesures de prĂ©vention en matiĂšre de santĂ©, de sĂ©curitĂ© et d’environnement et aux procĂ©dures/processus d’affaires du site de MontrĂ©al, les principales responsabilitĂ©s de l’OpĂ©rateur de fabrication sont les suivantes :

En tant que membre de l’équipe centrĂ©e sur les processus, l’OpĂ©rateur de fabrication est responsable de la fabrication de diffĂ©rentes formes posologiques et de l’exĂ©cution des diffĂ©rentes Ă©tapes des processus, telles que la pesĂ©e, la granulation, le mĂ©lange, la compression, l’encapsulation, l’enrobage et l’inspection des formes posologiques solides, semi-solides ou liquides, selon son domaine de spĂ©cialisation professionnelle, tout en respectant les diffĂ©rents critĂšres dans les dimensions suivantes : SĂ©curitĂ©, QualitĂ©, ExĂ©cution, CoĂ»ts et Personnel.

  • Nettoyer et entretenir les accessoires et les Ă©quipements de son secteur, ainsi que son poste de travail.
  • Effectuer l’étape de production sous sa responsabilitĂ©, rĂ©aliser les inspections et contrĂŽles requis et documenter ses actions conformĂ©ment au dossier de fabrication et aux fiches de travail standard.

Les tĂąches suivantes sont effectuĂ©es conformĂ©ment aux politiques, directives, procĂ©dures, dossiers de fabrication, Bonnes Pratiques de Fabrication (BPF/GMP), mesures de santĂ©, de sĂ©curitĂ© et de protection de l’environnement, procĂ©dures/processus d’affaires du site de MontrĂ©al, ainsi qu’au travail standard.


Formation, certification et expérience antérieure :

  • DiplĂŽme d’études secondaires ou Ă©quivalent.
  • La connaissance des BPF/GMP est un atout.
  • 2 ans d’expĂ©rience dans l’industrie pharmaceutique ou un secteur connexe est un atout.
  • Aptitudes mĂ©caniques et connaissances informatiques.


English Version:

Title: Manufacturing Operator

Duration: 6 Months

Location: Saint-Laurent, QC

Pay Rate: $28.96/hr

Note: Must be fluent in French and Candidates must be available to work any of the shifts, understanding that the shifts can change regularly.


Job Summary:

In compliance with established policies, guidelines, procedures, manufacturing records, and Good Manufacturing Practices (GMP), as well as health, safety, and environmental prevention measures and the business procedures/processes of the Montreal Site, the main responsibilities of the Manufacturing Operator are:

As a member of the process-centered team, the Manufacturing Operator is responsible for manufacturing various dosage forms and performing the different stages of the processes, such as weighing, granulation, blending, compression, encapsulation, coating, and inspection of solid, semi-solid, or liquid dosage forms according to their area of professional specialization, while respecting the different criteria in the following dimensions: Safety, Quality, Execution, Costs, and People.

  • Clean and maintain accessories and equipment in their area, as well as their workplace.
  • Perform the production stage under their responsibility, conduct the required inspections and controls, and document their actions according to the manufacturing record and standard work charts.

The following tasks are performed in compliance with established policies, guidelines, procedures, manufacturing records, Good Manufacturing Practices (GMP), health, safety, and environmental protection measures, business procedures/processes of the Montreal Site, as well as standard work.


Education, Certification, Previous Experience:

  • High school diploma or equivalent.
  • Knowledge of GMP is an asset.
  • 2 years of experience in the pharmaceutical or related industry is an asset.
  • Mechanical aptitude and computer knowledge.

Posted 6 days ago

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