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. 

Performs release of data and Certificate of Analysis(CofA) or Report of Analysis(RofA) based on document review in a timely and effective manner according to clients' methods, instructions, procedures,good laboratory documentation practices(GDP), good manufacturing practices(GMP) and standard operating procedures(SOPs) of SGS hEALTH Sciences Analytical Laboratories and  Departments. Assures OOS and deviations approved have no regulaltory complications. Reviews/revises SOPs for the purpose of corrective actions from internal and external audits. Generates responses to corrective actions from external audits. Trains analysts in GMP documentation. Performs Change control function as needed and other QA duties. Follow Training SOP for training and training records.

• Quality Assurance Professional understanding of the lab quality control / quality assurance processes, GMP and GDP as it relates to pharmaceutical testing records and C of A.
• As per SOP PSL-311-06.04 all employees must maintain appropriate attitude, constant vigilance and attention to detail.
• Incumbents are responsible for their own training records according to training SOP.
• Comfortable with LIMS System and other lab equipment to be able to perform audit trail of testing records 
• Well organized, autonomous and able to deliver good quality work efficiently
• Working knowledge of laboratory equipment systems to be able to perform audit trail of testing.
• Able / willing to learn new skills (review of new tests, instrumentation and procedures) as required and follow directions from management including priorities
• Technically competent
• Ability to learn quickly in a challenging environment.
• Excellent language, writing and communication skills required.
• Thorough knowledge of scientific principles pertaining to analytical records reviewed

• Ability to interpret, analyze data and draw logical conclusions required.

• Must be highly organized and able to work effectively and efficiently in a demanding environment with flexibility to changing priorities.
• Ability to work well with others, independently and fostering teamwork throughout the laboratory
• Proven time management skills and a strong attention to detail
• Responsible to deadlines
• Proficient in using various types of computer software (Word, Excel. PowerPoint & Outlook, LIMS and equipment software).
• Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
• Works well under pressure.
• Extended hours or weekend work may be required from time to time.
• Shift work may be required
• Appropriate attitude, constant vigilance, attention to detail and following Training SOP for training and training records.

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