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Grifols

Validation Intern

Grifols

Validation Intern at Grifols supporting validation engineering specialists with commissioning and data analysis. Role includes pre and post calibration of thermal monitoring equipment in a Montreal facility.

Posted 7/2/2026internshipMontreal • 🇨🇦 CanadaEntry LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates strong communication skills and accountability while supporting validation engineering activities in regulated environments. Proficient in maintaining calibrated equipment and monitoring data loggers, with a focus on compliance in the pharmaceutical or medical device industries.

Highest-signal resume keywords
Thermal Monitoring Equipment CalibrationValidation Engineering SupportFDA-Regulated Manufacturing ExperienceBilingual in French and EnglishStrong Verbal and Written Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Thermal Mapping Equipment MaintenanceSample CollectionData Logger MonitoringPre-Calibration and Post-CalibrationDocumentation Participation
Soft Skills
Effective CommunicationInterpersonal AbilitiesResponsibilityAccountabilityAbility to Work Independently
Industry Keywords
Pharmaceutical IndustryBiologicsBiotechMedical Device IndustryHealth Canada Regulations

About the role

Key responsibilities & impact
  • Support validation engineering specialists
  • Assist with pre- and post-calibration of thermal monitoring equipment
  • Maintain calibrated status of thermal mapping equipment
  • Monitor battery usage and age of wireless data loggers
  • Collect samples during cleaning, testing, and validation activities
  • Participate in documentation during commissioning
  • Communicate effectively and in a timely manner
  • Demonstrate responsibility and accountability within a team environment

Requirements

What you’ll need
  • Currently enrolled in an engineering or science program (Bachelor’s or Master’s in Chemical, Biomedical, Biological, or Biomanufacturing Engineering or Sciences)
  • Cumulative GPA of 3.00 or higher required
  • Experience in an FDA- or Health Canada-regulated manufacturing facility — pharmaceutical, biologics, biotech, or medical device industry is an asset
  • Ability to work independently with minimal supervision
  • Strong verbal and written communication skills and good interpersonal abilities
  • Bilingual in French and English preferred

Benefits

Comp & perks
  • Full-time 6-month internship in Montreal, Quebec between July and December
  • Medical and health coverage
  • Paid time off policy
  • Professional development opportunities
  • Flexible working hours