Stagiaire, opération de fabrication, Fractionnement, Manufacturing Operations Intern, Fractionation
About The Position
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. The Manufacturing Operations & Validation Intern’s principal responsibility is to support both commissioning and validation activities as well as Good Manufacturing Practice (GMP) operations.
Requirements
- Currently enrolled in an undergraduate program in Biotechnology, Chemical or Mechanical Engineering, Life Sciences, or a related field.
- Strong interest in pharmaceutical manufacturing and regulatory compliance.
- GPA of 3.00 or higher required.
- Available for a minimum of 8 months full time internship in Montréal, Québec from September 2026 to end of May 2027.
- Excellent attention to detail and organizational skills.
- Ability to work in a cleanroom environment and follow strict procedures.
- Must be able to work independently with minimum supervision and use good judgment.
- Able to keep neat, accurate and complete records and logs.
- Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
- Ability to meet deadlines, and handle an ever changing, fast paced critical work environment.
- Strong organizational skills, analytical and problem-solving skills. Ability to analyse details and perform structured decision-making on a daily basis.
- Proficiency with Microsoft office including Word, Excel, and PowerPoint. Experience in creating reports in Words and Excel. Microsoft Project and Visio a plus.
- Ability to lift or push up to 25 pounds.
- Good oral and written communication skills and good interpersonal skills.
Nice To Haves
- Bilingual in both French and English preferred (la maîtrise de l’anglais est requise pour assurer les échanges de documentations et communications avec d’autres sites de Grifols hors Québec et hors Canada (Espagne, USA).
Responsibilities
- Assist Validation Specialists in the commissioning and qualification of manufacturing equipment and cleanroom facilities.
- Participate in routine GMP manufacturing operations, including: Cleaning and sanitization of equipment and production areas. Preparation of materials and equipment for production.
- Contribute to the drafting and revision of Standard Operating Procedures (SOPs) related to manufacturing and cleaning processes.
- Collaborate with cross-functional teams including Quality Assurance, Quality Control, Engineering, and Production.
- Maintain accurate and detailed records in accordance with regulatory requirements.
- Adhere to all safety and compliance protocols.
- Demonstrate knowledge of proper aseptic techniques.
- Communicate effectively and promptly, escalate any issues that require management decisions.
- Demonstrate high levels of values and integrity.
- Demonstrate responsibility and accountability in a team environment.
Benefits
- Practical experience in a GMP-regulated environment.
- Exposure to industry-standard validation and commissioning processes.
- Understanding of pharmaceutical manufacturing operations and quality systems.
- Experience in SOP development and documentation practices.
- Mentorship from experienced professionals in the field.
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
Associate degree
