Job Description

A career with Canadian Analytical Laboratories provides an opportunity to work with a diverse group of people, from various backgrounds and professions, in an organization that is growing and evolving to make lives better and safer through analytical testing and research. www.cal-laboratories.com Job Summary: Perform activities of the Quality Assurance department in strict accordance with all Standard Operating Procedures, GMP, company policies and procedures. The key objective of this role is to work in all quality assurance systems and ensure they meet all relevant regulatory requirements of the pharmaceutical industry. Key Responsibilities:

• Review and maintain internal and external equipment calibration records
• Manage all aspects of quality documentation issuance and returns inclusive of all laboratory logbooks and notebooks
• Distribute SOPs and analytical procedures to laboratories and maintain QA documentation system.
• Maintain the process for the execution, investigation and documentation of all laboratory OOS occurrences
• Review stability protocols
• Maintain records for appropriate retention times
• Review standard receiving reports and approve reference standard labels
• Maintain overall CAPA program to include investigation, root cause analysis, corrective and preventative actions and documentation
• Review analytical raw data for the standards testing when required
• Take responsibilities of document reviewer in his/her absence
• Review analytical methods, standard operating procedures, method validations and method transfer studies when required
• Assist QA Manager in performing annual trending reviews
• Assist QA Manager in hosting GMP audits from clients and regulatory agencies such as Health Canada
• Assist QA Manager in identifying and implementing continuous improvement initiatives
• Maintain QA activities in the absence of reporting line

Minimum Requirements:

• Degree in the scientific discipline or equivalent
• Minimum 2-4 years? experience in the area of pharmaceutical quality assurance
• Good knowledge of GMP, chemical and microbiological concepts
• Ability to organize, communicate, and work with others in an effective manner
• Working knowledge of basic computer systems and software applications

Canadian Analytical Laboratories would like to thank all applicants; however only candidates selected for interviews will be contacted. Laboratory Operations During COVID-19: As an essential service provider, Canadian Analytical Laboratories is open to continue to support our community. We continue to closely monitor the COVID-19 situation as well we are working to comply with advice being provided by both levels of the Canadian government. Our parent company, Reena Group provides essential goods and services to the pharmaceutical, food, natural health products and medical cannabis industries, who are playing a pivotal role in responding to the crisis by ensuring the availability of products and supplies necessary to respond medically and economically both in Canada and the United States. During this unprecedented time, our number one priority is the safety of our employees, customers and communities. To continue to serve our laboratory client community, we have proactively adopted modified working practices, staggered working hours and taken all the warranted precautions to mitigate the risk of COVID-19 transmission and to ensure a safe environment to ensure that we comply with the principles of social distancing. Job Types: Full-time, Permanent Benefits:

• Dental care
• Extended health care
• Vision care

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Mississauga, ON: reliably commute or plan to relocate before starting work (preferred)

Education:

• Bachelor's Degree (preferred)

Experience:

• Pharmaceutical Laboratory QA: 2 years (preferred)

Work Location: In person