Stagiaire en Validation - Validation Intern

GRIFOLS, S.A.•Montreal, QC

2d•Onsite

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.

Requirements

Currently completing an Engineering or Science degree (Bachelors or Masters in Chemical, Biomedical, Biomanufacturing, Biological Sciences or Engineering)
GPA of 3.00 or higher required
Available for a 6 month full time internship in Montréal, Québec from July to end of December
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.
Ability to lift or push up to 25 pounds.
Good oral and written communication skills and good interpersonal skills

Nice To Haves

Experience in an FDA or Health Canada regulated manufacturing facility – pharmaceutical, biologics, biotech, or medical device industry is preferred.
Microsoft Project and Visio a plus.
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

Support validation engineering specialists through assistance with commissioning, verifying drawings, components, parts, P&ID, testing and protocol execution, and data analysis.
Participate in pre and post calibrations of thermal monitoring equipment, placing probes and generating reports and graphs of data.
Maintain calibrated state of thermal mapping equipment
Monitor use and age battery life of wireless loggers.
Collect samples during cleaning, testing and validation, as well as generate test forms and submit samples to QC.
Participate in documentation during commissioning, Prelim T-Study, protocol execution in support of validation engineer protocols, as assigned.
Assist with ensuring paperwork from other departments is available and complete when required.
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.
Strong computer skills; communication and interpersonal skills.
Detail oriented.
Must be flexible with working hours.