GMP Technician - Jobs in Greater Napanee, ON

Job Description

VIVO Cannabisâ„¢ is recognized for trusted, premium cannabis products and services. It holds production and sales licences from Health Canada and operates world-class indoor and seasonal airhouse cultivation facilities. VIVO has a collection of premium brands, each targeting different customer segments, including Canna Farmsâ„¢, Beacon Medicalâ„¢, Firesideâ„¢, Fireside-Xâ„¢, Luminaâ„¢ and Canadian Bud Collectionâ„¢. Harvest Medicine, VIVOs patient-centric, scalable network of medical cannabis clinics, has serviced over 150,000 patient visits. VIVO is pursuing several partnership and product development opportunities and is focusing its international efforts on Germany and Australia.The OpportunityAre you an energetic, passionate people professional with an exceptional interpersonal skill set Do you enjoy helping employees to navigate questions and challenges Do you understand how to engage to deliver results across functional teams and among competing priorities Have you developed incredible organizational and time management skills Are you eager to learn and be part of a dynamic business in an exciting industryIf so keep reading to learn about an exciting new opportunity to join VIVO Cannabis on our journey to create, grow and deliver excellence outcomes in the cannabis space focused primarily on health and wellness!Position OverviewVIVO s licensed producer, ABcann Medicinals, in Napanee, Ontario is seeking a GMP Technician to support the on site quality assurance team. The GMP Technician will support all aspects of quality assurance activities related to EU-GMP activities at the site level as directed by the Quality Assurance Manager (Quality Assurance Person).Key Responsibilities

• Assist the Quality Assurance Manager (Quality Assurance Person) in managing the Validation Program for the Napanee Facility.
• Ensure compliance with international EU-GMP Regulations for applicable markets – eg. Germany, Australia, Israel, etc.
• Write, review, and update validation and qualification documents as needed.
• Participate in execution of validation documents.
• Assess new equipment to determine if validation/qualification/calibration is required based on the intended use, add to the Validation and Calibration Programs as needed.
• Work with the QA Team writing, reviewing, and updating Standard Operating Procedures (SOPs) and quality policies/procedures as they pertain to both QA and EU-GMP activities.
• Ensure continued compliance with GMP regulations as well as the Cannabis Act, Controlled Drugs and Substances Act (CDSA), Narcotics Control Regulations (NCR), Pest Control Products Act (PCPA), Fertilizer Act, GPP, and HACCP, and other relevant legislation and standards.
• Assist with internal and external audit programs, as needed.
• Assist in preparation of quality related reports (CAPA, Deviation and Investigation).
• Assist with maintenance and execution of the calibration program.
• Required to complete all training for a Quality Assurance Technician.
• Any other responsibilities defined in the SOP’s listed in the associated curriculum for Quality Assurance Technician.
• Other duties, as assigned by the Quality Assurance Manager (QAP).

Qualifications and SkillsAcademic/Educational Requirements

• BSc or Diploma or degree in a science related field

Required Skills/Experience/Knowledge

• 1-3 years Quality Assurance experience in GPP/GMP manufacturing fields, preferably within Pharmaceutical, Legal Cannabis, Food Industry or any other relevant industry is considered an asset
• 1-3 years Validation and Qualification experience is preferred
• Previous Health Canada Security Clearance and work experience with a Canadian Licensed Producer (LP) is considered as an asset
• Ability to obtain a Health Canada Security Clearance is a requirement
• Experience with technical report writing and scientific documents an asset
• Knowledge of quality assurance and validation terminology, methods, and tools
• Strong computer skills; including but not limited to MS Office Suite and Smartsheet
• Strong organizational skills, including the ability to manage time, set priorities, and multi-task with minimum supervision
• Excellent attention to detailMust possess excellent communication skills (English, written and verbal) for liaising and communicating with internal departments and service providers/clients
• Excellent critical thinking, problem solving and decision-making skills
• Motivated to work in a dynamic and fast-paced team environment
• May require occasional evening or weekend work as needed and to accommodate different time zones for our clients

Job Type: Full-timeSchedule:

• 8 hour shift

Quick Apply

• Terms & Conditions
• New Privacy
• Privacy Center
• Accessibility

For Job Seekers

• Browse Jobs
• Advanced Job Search
• Emplois Quebec

For Employers

• Post a Job

Stay Connected