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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.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
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