Manufacturing Operations Intern, Fractionation

Grifols

Manufacturing Operations Intern at Grifols focusing on GMP operations and validation activities. Collaborating with cross-functional teams and maintaining accurate production records.

Posted 6/8/2026internshipMontreal • 🇨🇦 CanadaEntry LevelWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Good Manufacturing Practices (GMP)aseptic techniquescleanroom environmentBiotechnologyChemical EngineeringMechanical EngineeringLife Sciencesregulatory complianceattention to detailanalytical skills

Soft Skills

communication skillsinterpersonal skillsorganizational skillsproblem-solving skillsaccountabilityindependencejudgmentability to meet deadlinesteam collaborationintegrity

Tools & Technologies

Microsoft OfficeMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft ProjectMicrosoft Visio

Industry Keywords

standard operating procedures (SOPs)manufacturing equipmentproduction areascross-functional teamsQuality AssuranceQuality Controlrecord keepingsafety protocolscompliance protocolsfull-time internship

About the role

Key responsibilities & impact

Assist validation specialists with the commissioning and qualification of manufacturing equipment and cleanrooms.
Participate in routine manufacturing operations in accordance with Good Manufacturing Practices (GMP), including:
Cleaning and disinfecting equipment and production areas.
Preparing materials and equipment for production.
Contribute to the drafting and review 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 compliance with regulatory requirements.
Adhere to all safety and compliance protocols.
Demonstrate knowledge of appropriate aseptic techniques.
Communicate effectively and promptly, escalating issues that require management decisions.
Uphold high standards of values and integrity.
Demonstrate accountability within a team environment.

Requirements

What you’ll need

Currently enrolled in a university program in Biotechnology, Chemical or Mechanical Engineering, Life Sciences, or a related field.
Strong interest in pharmaceutical manufacturing and regulatory compliance.
A minimum cumulative GPA of 3.00 is required.
Available for a full‑time internship of at least 8 months in Montreal, Quebec, from September 2026 to the end of May 2027.
Excellent attention to detail and organizational skills.
Ability to work in a cleanroom environment and follow strict procedures.
Able to work independently with minimal supervision and exercise good judgment.
Able to maintain neat, accurate, and complete records and documentation.
Strong interpersonal skills and the ability to interact professionally with personnel at all levels.
Ability to meet deadlines and manage a fast‑paced, dynamic, mission‑critical work environment.
Strong organizational, analytical, and problem‑solving skills.
Ability to analyze details and make structured decisions on a day‑to‑day basis.
Proficiency in Microsoft Office, including Word, Excel, and PowerPoint.
Experience creating reports in Word and Excel. Microsoft Project and Visio are assets.
Ability to lift or push up to 25 pounds.
Good oral and written communication skills and strong interpersonal abilities.
Bilingual in French and English preferred.

Benefits

Comp & perks

Hands‑on experience in a GMP‑regulated environment.
Exposure to commissioning and validation processes aligned with industry standards.
Understanding of pharmaceutical manufacturing operations and quality systems.
Experience developing standard operating procedures and documentation practices.
Mentorship from experienced industry professionals.