Validation Analyst – Pharma
Position : Validation Analyst Pharma
Location : Montreal
Do you thrive in a dynamic environment and have a passion for developing and validating analytical methods?
Are you a highly motivated chemist eager to make a real impact in a growing company?
We're seeking a talented Analytical Chemist to join our team! This is a brand-new role, offering you the opportunity to shape the future of our analytical processes.
The Offer :
- Competitive salary with an annual bonus between 4% and 8%
- Comprehensive Benefits : 3 weeks of vacation, 4 sick days, 3 personal days, retirement savings plan with a 3% company match, and 90% company-covered health insurance
- Work-life balance : o nsite position with a flexible schedule (core hours 10-3, corporate summer hours with Fridays off at 1 pm)
- Great Location : o ffices are conveniently located in TMR (Ferrier)
Must Haves :
- Industry expertise : at least 5 years of experience in the pharmaceutical industry, specifically with method development and validation (non-negotiable)
- Bilingual to communicate with clients in Toronto and the US
- Demonstrated expertise in various analytical techniques, including HPLC, GC, FTIR, Atomic Absorption, and Dissolution
- Strong understanding and applies Good Laboratory Practices (GLP) consistently
- Excellent written and technical communication skills
- Team player with exceptional organizational and planning abilities
- Ordre des chimistes du Québec membership is an asset (not mandatory)
Why You'll Love Working Here :
- This is a new role, allowing you to take your place in a great team
- Collaborative Spirit : our client has a strong team atmosphere with excellent leadership and an emphasis on cross-collaboration
- Investment in growth : t he company is rapidly expanding, adding new products and constantly innovating
- Diverse product portfolio : work with a variety of exciting products, including tablets, capsules, liquids, and creams
Your Responsibilities :
- Develop, optimize, and validate analytical methods in accordance with regulatory requirements
- Support analysts in resolving analytical issues
- Participate in the analysis of various R&D products
- Contribute to project planning and scheduling
- Verify and propose methods for ingredients and developed products (including USP methods)
- Collaborate on investigations of Out-of-Specification (OOS) results
- Perform qualification analyses for raw materials and finished products
- Train analysts on new analytical methods
Please send your resume in Word format to Maia Slivinschi at maia. .
REFER A PERM HIRE AND EARN UP TO $1,000! For more details, click here .
OUR VIRTUAL DOORS ARE OPEN! We’re also bringing the interviews to you by various web applications, virtually! Contact us today for your next opportunity.
CNESST permit number : AP-2000158