Career Category

Job Description

Title: Sr Associate Quality Assurance (1 Year Contract)

Reports to: Sr Manager QA

Location: Mississauga Head Office

Job Summary

Working at Amgen
At Amgen you’ll experience a work environment where employees strive to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health. Amgen provides the working environment you have always strived for - A perfect combination of science and entrepreneurship that brings therapies to market by people that have a true passion for their work.

Our culture is what makes Amgen a special place to work. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. Take a few minutes to hear what some of our current staff members are sharing about working at Amgen. Click HERE

Responsibilities: 

• Review batch documentation for commercial and clinical products and disposition as per Standard Operating Procedures (SOPs)
• Participate as QA Owner/QA Contact for Deviations, Corrective/Preventive Actions (CAPAs), Complaints, and Temperature Excursions (TEs)
• Review Annual Product Reviews (APRs) for commercial products    
• Schedule, compile, review, and coordinate filing of Yearly Biologic Product Reports (YBPRs) for commercial products    
• Review Stability Summary Reports
• Review Executed Batch Records  
• Draft SOPs, Protocols, Technical Reports, and memos in support of Quality activities
• Run stability data reports, assess data, and issue memos in support of TEs for Amgen products
• Complete Quality launch milestones
• Develop and deliver GMP training
• Represent IDQ Canada from internal/external audits and inspections  
• Represent IDQ Canada at cross-functional meetings for complaints, disposition, and launch
• Represent IDQ Canada as a Subject Matter Expert (SME) during internal/external audits and inspections
• Ensure compliance with Canadian Food and Drugs Act and current Good Manufacturing Practice (GMP) regulations
• Ensure compliance with Good Distribution Practice (GDP) regulations
• Liaise with other divisions within the Canadian office, U.S. Head Office, and other international affiliates to exchange information to meet objectives
• Perform other quality tasks and projects as assigned by Manager

Basic Qualifications

BSc degree

Preferred Qualifications

• 3+ years of Pharmaceutical Industry experience in a Quality Assurance role
• Bachelor’s Degree in the Physical or Biological Sciences
• Strong understanding of the Pharmaceutical and Biotechnology Industries
• Understanding of Health Canada GMP Regulations, specifically as they relate to drug product importation
• Understanding of Health Canada GDP Regulations
• Prior product disposition experience
• Prior experience reviewing executed batch records
• Strong problem-solving skills, with sound judgment and the ability to make decisions independently while balancing business needs, quality and compliance risk
• Strong organizational skills and an ability to manage multiple tasks and responsibilities in a dynamic work environment 
• Ability to follow assignments through to completion and meet timelines
• Excellent communication and interpersonal skills
• Strong attention to detail and critical-thinking 
• Prior experience using SAP and Quality Management System (QMS) applications
• Advanced experience using Microsoft Office software (Word, Excel, PowerPoint)

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Amgen endeavors to make its recruitment process accessible to any and all users. Reasonable accommodations will be provided, upon request, to applicants with disabilities in order to facilitate equal opportunity throughout the recruitment and selection process. Please contact TalentAcquisitionInquiries@amgen.com to make a request and ensure you include the requisition number.

Reasonable accommodations are available, upon request, to facilitate the equal participation of candidates with disabilities, should you be selected for an interview.