WE ARE SGS – THE WORLD’S LEADING TESTING, INSPECTION AND CERTIFICATION COMPANY. WE ARE RECOGNIZED AS THE GLOBAL BENCHMARK FOR QUALITY AND INTEGRITY. OUR 89,000 EMPLOYEES OPERATE A NETWORK OF 2,600 OFFICES AND LABORATORIES, WORKING TOGETHER TO ENABLE A BETTER, SAFER AND MORE INTERCONNECTED WORLD. 

• Review and Approve investigations related to equipment and RND studies
• Be active back up for review and approval of all other type of OOS and deviation investigations
• Review and approve CCRs and SOPs for equipment
• Review and approve stability protocols, reports and CCRs.
• Review and approve equipment related protocols, and reports
• Be DMS/TMS site representative and manage all the activities for newly implemented programs
• Maintain client test methods and specification data bases
• Secondary Reference Standard COA review
• Perform internal audits and follow ups for effectiveness.
• To maintain vendor evaluation program
• Coordinate with clients and legal for quality agreements, maintain the data base and records
• Periodic review of Undelete for deleted items
• Review of area monitoring charts
• Weekly review of logbook, email raw data to clients
• Be backup for QA Associate

• A minimum of a BSc degree (or equivalent) is required. 
• Over three years of related experience in a pharmaceutical environment
• Previous experience in a Quality Assurance related role would be preferred. 
• Must be able to prepare compliant to regulations protocols and reports. 
• Must be capable to notice any GMP deficiencies in reports 
• Candidates must be proficient in using various type of computer software (Word, Excel, Outlook etc.).

SGS Canada is an equal opportunity employer and we are committed to achieving greater accessibility by providing accommodation for people with disabilities during our hiring process.  Accommodations are available on request for qualified candidates during each stage of the recruitment process.

Please note that candidates applying for Canadian job openings should be authorized to work in Canada