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 : onsite position with a flexible schedule (core hours 10-3, corporate summer hours with Fridays off at 1 pm) - Great Location : offices 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 : the 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.

[email protected]. 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