Technicien de fabrication - Manufacturing Technician

at  G Canada Therapeutics

Aimeriez-vous vous joindre à une équipe internationale qui oeuvre à améliorer le futur des soins de santé ? Voulez-vous améliorer la vie de millions de personnes ? Depuis sa fondation à Barcelone en 1909, Grifols est une société d’envergure mondiale de soins de santé qui s’efforce d’améliorer la santé et le bien-être des populations du monde entier. Nos quatre (4) divisions – Bioscience, Diagnostique, Hôpitaux et Produits biologiques développent, produisent et commercialisent des médicaments innovants, des solutions et des services dans plus de 100 pays et régions.
Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies - develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.

QUALIFICATIONS REQUISES :

• Diplôme d’études secondaires. Diplôme d’études collégiales ou collégiales en technologie pharmaceutique ou diplôme universitaire en génie ou en sciences de préférence.
• Une expérience minimale de 1 an dans l’industrie biopharmaceutique, pharmaceutique et des soins de santé est préférable.
• Capacité de travailler dans un environnement au rythme rapide et de gérer de multiples priorités
• Capacité de travailler de manière indépendante ainsi que dans un environnement d’équipe
• Doit être capable de soulever au moins 15 kg et de porter de l’EPI au besoin
• Certaines tâches impliqueront de travailler dans un environnement réfrigéré
• Une expérience dans l’exploitation des salles propres est un atout
• Bilinguisme (français et anglais) à la fois parlé et écrit

QUALIFICATIONS:

• High School Diploma. CEGEP/College diploma in pharmaceutical technology or University degree in Engineering or Science preferred.
• Minimum 1-year experience within the biopharmaceutical, pharmaceutical, healthcare industry is preferred.
• Ability to work in a fast-paced environment and manage multiple priorities
• Ability to work independently as well as in a team environment
• Must be able to lift at least 15kg and wear PPE as required
• Some tasks will involve working in a refrigerated environment
• Experience in clean room operation is an asset
• Bilingualism (French and English) both spoken and written
  Location: NORTH AMERICA : Canada : Montreal:CAQUEBEC - Quebec
  Learn more about Grifols

PURPOSE STATEMENT

The Manufacturing technician will be primarily assigned to one of the following areas: Fractionation, Purification, Fill/Finish or Packaging but will be expected to develop multi-disciplinary skills by alternating to other areas of Manufacturing to assist with business demands. The Manufacturing technician is working in a manufacturing environment regulated by cGMPs, SOPs, safety procedures and all company policies/regulations.

KEY DUTIES AND RESPONSIBILITIES

• Set up, operation and cleaning the following equipment (depending on the designated Manufacturing area): Buffer Preparation Skids, Centrifuge, Fractionation Skids and Filter presses, TFF Skids and columns, Chromatography Skids, Filtration Skids and Filling line (within an isolator)
• Set up and operation: CIP/ SIP Skids, Autoclaves and Parts Washers
• Execution of all Manufacturing batch records in the designated areas based on the training completed within that area
• Escalation of all of issues potentially impacting cGMP of the respective Manufacturing area and or Manufacturing process to the responsible manager immediately
• Participate in all Manufacturing activities related to the assigned area including sampling (process and cleaning validation, environmental monitoring, clean utilities), in-process testing, weighing, calibration and maintenance of equipment (pH meter…)
• Actively participate in writing and implementing GMP documents (SOPs, batch records) using the change control system and maintain records of all necessary information/data as per GDPs
• Execute daily, weekly and monthly cleaning in the respective Manufacturing area following the applicable standard operating procedures
• Ensure all Manufacturing supplies within the respective Manufacturing area are maintained and replenished as required