22 May

Associate Pharma Jobs Vacancy in Cannabis Brantford

Position
Associate Pharma
Company
Cannabis
Location
Brantford ON
Opening
22 May, 2018 30+ days ago

Cannabis Brantford urgently required following position for Associate Pharma. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Associate Pharma Jobs Vacancy in Cannabis Brantford Jobs Details:

Up Cannabis is a federally licensed producer of medical cannabis with an operational facility in Brantford, Ontario and a new facility currently under construction in Beamsville, Ontario. Up is wholly owned by Newstrike Resources, which is a publicly traded company on the TSXV and trades under the ticker symbol "HIP".

General Responsibilities:

Reporting directly to the QA Manager, this role is responsible for ensuring consistent quality of product. The QA Associate must have a deep understanding of compliance requirements that meet or exceed Health Canada as well as internal requirements.

Key Responsibilities:

  • Quality System maintenance and management
  • Review and control of Canadian printed packaging components (including master label artwork);
  • Documentation review of all GPP documents;
  • Review and control of Canadian production and packaging documents;
  • Analytical finished product testing and Finished Product Specifications;
  • Finished product release to Canadian distribution system based on conformance of finished product to all manufacturing and Quality Control/Assurance standards for the Regulated Products and all applicable GPPs, which includes: Batch Documentation Review, Certificate of Analysis Review, Label Review, Sample Handling and Release of Finished Product;
  • Handling and review of any necessary investigations arising out of complaints regarding quality;
  • Handling and review of any product retrievals or recalls;
  • Ensuring all levels of change are evaluated and documented;
  • Investigate Out of Specification results;
  • Coordinating and overseeing destructions;
  • Investigations associated with Pharmacovigilence Activities (Adverse Events);
  • Validation Protocols and Reports including but not limited to, Process Validation, Cleaning Validation and Method Transfers/Validations;
  • Annual Product Quality Review creation and maintenance

Stability Program Work including:

  • Review and assess for compliance data from stability programs for the Regulated Products;
  • Set-up and Review of Stability Programs including Stability specifications
  • Write, review, revise and maintenance of Standard Operating Procedures as they pertain to the production, distribution and sale of the Regulated Products in Canada;
  • Preparation and maintenance of regulatory documents (i.e.: Producers Licence) as they relate to the Regulated Products;
  • Audits of sites on behalf of the Licensed Producer;
  • Supervision and Representation at Health Canada Inspections on behalf of the Licensed Producer; and
  • Provide GPP training to staff members.

Requirements:

  • Bachelor of Science
  • Certificate in Pharmaceutical Regulatory Affairs & Quality Operations preferred
  • 2-3 years relevant experience with in the pharmaceuticals, biotech or healthcare industries in regulatory/compliance
  • Strong knowledge of current Canadian GMP regulations and guidelines
  • Previous experience writing SOPs and technical writing and document management
  • Proficient in the use of Microsoft Office suite
  • Ability to work independently, and as part of a team and collaboratively across the organization
  • Ability to prioritize and schedule daily activities, manage multiple priorities, and requests under tight time constraints
  • Excellent analytical and problem solving skills
  • Outstanding communication skills, written and verbal
  • Clean police background check
  • Patient/Customer focus, results oriented with excellent organizational skills

Job Type: Full-time

Experience:

  • pharmaceuticals: 2 years

Education:

  • Bachelor's


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