Computer Science Intern Jobs in Quebec (NOW HIRING)

- Bilingue en francais et en anglais de preference (la maitrise de l'anglais est requise pour assurer les echanges de documentations et communications avec d'autres sites de Grifols hors Quebec et hors Canada (Espagne, USA). 

Ce que vous gagnerez : 

- Experience pratique dans un environnement reglemente par les BPF. 

- Exposition aux processus de validation et de mise en service conformes aux normes de l'industrie. 

- Comprehension des operations de fabrication pharmaceutique et des systemes de qualite. 

- Experience dans l'elaboration de procedures operatoires normalisees et des pratiques de documentation. 

- Mentorat par des professionnels experimentes dans le domaine. 

Position Title: Manufacturing Operations Intern, Fractionation - 8 months from September 2026 to May 2027 

Reports to: Supervisor, Fractionation 

Position Summary: 

The Manufacturing Operations &Validation Intern's principal responsibility is to support bothcommissioning and validation activitiesas well asGood Manufacturing Practice (GMP) operations. 

Key Duties and Responsibilities: 

• Assist Validation Specialists in thecommissioning and qualificationof manufacturing equipment and cleanroom facilities. 

• Participate inroutine GMP manufacturing operations, including: 

• Cleaning and sanitizationof equipment and production areas. 

• Preparation of materials and equipment for production. 

• Contribute to thedrafting 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. 

Qualifications: 

• Currently enrolled in an undergraduate program inBiotechnology, 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 Montreal, Quebec 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 

• Bilingual in both French and English preferred (la maitrise de l'anglais est requise pour assurer les echanges de documentations et communications avec d'autres sites de Grifols hors Quebec et hors Canada (Espagne, USA). 

What You'll Gain: 

• 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.