Quality Control Specialist - Pharmaceutical - Hybrid

Position: Quality Control Specialist - PharmaceuticalLocation: Ville Saint-LaurentSalary: $35-$40 per hour Job Type: 6-month contractSchedule: 4 days / week - 29 hours a weekAre you a quality professional with deep experience in pharmaceutical, biologic, or combination product environments? Our client is seeking a Quality Control Specialist with a full understanding of GMP to provide independent quality support across regulated products and processes.Why This Role Matters:- Apply your GMP expertise to ensure compliance across pharmaceuticals, biologics, devices, combination products, and cosmetics.- Collaborate with cross-functional teams while driving quality initiatives that impact products from receipt through distribution.- Play a key role in audits, CAPA investigations, supplier oversight, and quality system improvements.Key Responsibilities:- Ensure all commercial quality activities comply with GMP/GDP regulations and local/global quality standards.- Develop, implement, and optimize quality systems, procedures, and processes.- Lead or support internal, external, and regulatory audits.- Review and approve quality documentation, including change controls, product quality reviews, and supplier assessments.- Investigate deviations and non-conformances, implementing CAPA and corrective measures.- Execute supplier qualification programs and monitor performance of key suppliers.- Ensure compliance with Good Storage and Distribution Practices, including controlled-temperature shipments.- Represent Commercial Quality in cross-functional projects and programs.Requirements:- Bachelor's degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or related technical/scientific discipline.- 2+ years of quality assurance experience in pharmaceutical, biologic, or combination product environments.- Full understanding of GMP and practical experience applying it across regulated products.- Familiarity with SAP, TrackWise, ComplianceWire, OneVault, or similar quality systems.- Experience working both independently and collaboratively in cross-functional teams.- Strong ownership, decision-making, and problem-solving skills.Other Language Requirements: English- Level of Proficiency Required: Advanced- Reasons for Language Requirement: To communicate and support operations in other regions outside of Quebec- Frequency of Use: Daily (for various tasks)This is an excellent opportunity for experienced pharma/biopharma quality professionals who want to leverage their GMP expertise to make a real impact in a regulated, high-standard environment.Please forward your resume in Word format to Cristina Bilbao at cristina.bilbao@quantum.ca. REFER AND EARN A $50 GIFT CARD! 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 numbers: AP-2000158 & AR-2000157