Senior Specialist, Quality Services

Job Description Summary

At Paladin Pharma, we strive to offer a work environment that meets the diverse needs of our team members and advances the goals of the individual, the team and the company, while promoting flexibility, accountability and collaboration. If you're looking for a hybrid work environment, Paladin is the place for you!

This position requires a presence at our office located in St-Laurent, Montreal, two days a week, on Tuesdays and Wednesdays.

Reporting to the Quality Services Manager, the main responsibility of the Senior Specialist is to provide expert quality guidance, review, approval and is the quality lead for product technology transfers and validations throughout the products’ lifecycle to ensure that all activities related to manufacturing, packaging, testing and distribution meet current regulatory standards in approved markets and company standards. The Senior Specialist QS also provides oversight and guidance for the development and validation of analytical methods.

Job Description

• Leads in the resolution of investigations, deviations, corrective actions, and other quality issues with each CMO.
• Manages change controls under their responsibility.
• Evaluates metrics to determine trends and opportunities for continuous improvements and liaises with other departments.
• Performs risk assessments as necessary and identifies mitigations to reduce risks.
• Ensures procedures, master product records, specifications and related documents are initiated and maintained according to product lifecycle changes.
• Ensures product transfer and validation activities meet current regulatory requirements.
• Recommends process improvements based on process/method validation and compliance trends.

Your Profile

• Bachelor’s degree in science.
• 8+ years of experience in quality and validation in a GMP environment in the pharmaceutical and/or medical device industry.
• Demonstrates expert knowledge and application of the principles, concepts and theories of Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs), GXP/ISO standards, concepts, regulations and industry standards.
• Strong attention to detail.
• Strong technical writing skills and a good command of general grammar and usage.
• Demonstrates excellent interpersonal skills.
• Bilingual (French and English) with excellent oral and written communication skills.

What We Offer

• Hybrid work schedule
• Benefits package on first day
• Retirement Savings Plan (RRSP)
• Employer contribution to employee RRSP (DPSP)
• Employee Assistance Program (EAP)
• Telemedicine program
• Employee Referral Program ($)
• Free gym on site
• Free parking

Commitment to Diversity, Equity, and Inclusion:

At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.

About Us:

Headquartered in Montreal, Canada, Paladin Pharma is a leading specialty pharmaceutical company focused on acquiring or in-licensing new pharmaceutical products for the Canadian market. Its dedicated employees have made Paladin one of Canada's pioneering specialty pharmaceutical companies.

Paladin is an operating company of Endo USA, Inc, a highly specialized pharmaceutical company that brings quality branded and generic products to patients through excellence in development, manufacturing, and marketing.

To learn more about us, visit our website at www.paladin-pharma.com