ROSE LIFESCIENCE

About ROSE LIFESCIENCE

About ROSE ROSE LifeScience, a Quebec-focused cannabis company founded by executive leaders from the world’s largest government regulated industries, is currently seeking someone to lead its QA team at its facility in Huntingdon, Quebec. Currently finishing construction, ROSE’s Phase 1 site will produce high quality cannabis in its state-of-the-art indoor controlled facility. ROSE is also partnered with Tilray and represents their High Park brands exclusively in Quebec. General Responsibilities Write, review and maintain Standard Operating Procedures Ensure that all activities are carried out as per Standard Operating Procedures to produce consistent quality cannabis products Ensure all technical documents in use are current and all master documents such as policy documents and Standard Operating Procedures are controlled and secured in accordance with GPP Establish and maintain record keeping systems and ensure employee adherence to proper documentation practices Investigate deviations Review and approve incoming materials as needed Review quality complaints and lead investigations including corrective action and preventive action Oversee premises, hygiene of personnel, equipment cleanliness and maintenance Review method validation and equipment qualification protocols and reports (water system and HVAC) Implement standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of products Assure compliance to in-house and external specifications and standards Perform internal audits and vendor evaluation audits on a regular basis to determine quality qualifications. Actively participate in external audits such as regulatory inspections. Conduct recalls if needed Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary Assist product support areas in gathering and analyzing data Management and Teamwork Collaborate with other departments to ensure compliance with regulations Ensure that all personnel are trained and that records of training are kept Train staff on SOPs and working instructions Manage and coordinate staff, create department efficiencies and provide leadership support Communicate effectively to all levels of management Education & Experience Minimum of a Bachelor’s Degree in a basic science or related discipline (preferably chemistry or biochemistry). Minimum 10 years of experience working in Quality Assurance in a GMP environment and/or pharmaceutical industry Must have extensive knowledge of good production practices and/or good manufacturing practices Skills, Knowledge & Abilities Ability to understand, create, and follow documented procedures Ability to follow direction and carry out tasks independently Attention to detail and ability to work cleanly and methodically The ability to work quickly, efficiently, and reliably in a fast-paced work environment Good interpersonal and communication skills The chosen applicant will be required to successfully complete criminal and reference checks. Required to work weekends and holidays Job Types: Full-time, Permanent

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Company Info

Legal Form: Inc

Company Type: Private

Company Size: 51 - 250

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