Full job description

If you are looking to work for a growing, Canadian company that is focused on the transportation and storage of pharmaceutical, medical and healthcare products across Canada then Rogue Transportation has a career for you

We are an employer that works to build great leaders, teams and businesses. We know our employees are key to everything we accomplish, so we give them the freedom and resources to reach their potential and the opportunity to work with managers who care about their professional development. We value integrity, encourage collaboration, celebrate passion, reward creativity, and demand excellence — because our customers deserve nothing less and our customers are at the heart of every one of our goals.

As a part of Rogue Transportation, you can enjoy an exciting career, a company culture based on a clear purpose and values, and the knowledge that your work makes a real difference. If you would like to learn more about us, we would love to hear from you.

Rogue Transportation is seeking a full-time Quality Assurance Supervisor to join our team

POSITION SUMMARY:

The Quality Assurance Supervisor is responsible for managing the Drug Establishment License for our primary warehouse facility in Mississauga and ensuring that we maintain our license in good standing with Health Canada’s requirements. The QA Supervisor will also be responsible for performing audits of partner carriers and third-party GMP to ensure that meet our pharmaceutical customers requirements. This position is responsible for the administration and management of quality agreements with carriers, warehousing, wholesalers and pharmaceutical manufacturers. This position is the key liaison officer for all third-party site GMP related matters with the Canadian government, manufacturing sites, and head office.

QUALIFICATIONS

• Minimum of Bachelor Degree in Science required with a minimum of three years of experience in pharmaceutical/medical /food quality assurance
• Prior experience in the healthcare or pharmaceutical industry is required
• Qualified Pharmaceutical GMP and GLP auditing experience required
• Detailed knowledge of DEL required
• Experience in Management of QA/QC and sanitation logs and records; verification of QA/QC and sanitation activities records as requested by QA Audit department and reporting to management
• Experience in overseeing safety of employees and work environment; Participating in Safety Committee
• Experience in managing and monitoring Temperature controlled facilities and trucks
• Detailed knowledge of Canadian GMP required
• Knowledge of FDA drug regulations an asset
• Knowledge and working relationship with Health Canada personnel is desirable
• Medical device and sterile instrumentation knowledge is an asset

SKILLS

• Strong understanding of Canadian, US and EU GMP Regulations
• Excellent communication skills (written and verbal)
• Excellent customer service skills and the ability to collaborate with all levels both inside and outside the organization
• Strong computer skills in Microsoft Office 365
• Self-motivated and able to work with minimal supervision
• Experience in writing and updating SOPs is required
• Strong attention to detail with the ability to multitask and handle fluctuating workloads
• Excellent organizational and problem-solving skills
• Excellent continuous improvement skills
• Proven ability to adhere to standards and procedures and maintain confidentiality
• Proficient in documenting and writing reports
• Understanding of NCRs and CAPA systems and equipment validations is an asset

Job Type: Full-time

Benefits:

• Casual dress
• Dental care
• Extended health care
• On-site parking
• Vision care

Flexible Language Requirement:

• French not required

Schedule:

• Monday to Friday
• Weekends as needed

Education:

• Bachelor's Degree (preferred)

Experience:

• quality assurance: 3 years (preferred)

Work Location: In person

Application deadline: 2024-07-26
Expected start date: 2024-07-29