Skip to main content
Post your resume and find your next job on Indeed!

Medical Biotech jobs in Vancouver, BC

Sort by: -
    • Senior-level experience in Quality within pharma or biotech.
    • We are seeking a Part-Time Quality Director (remote) to provide oversight of GMP and regulatory…
    • We are seeking a Fermentation Specialist with expertise in anaerobic and aerobic fermentation to lead process development, optimization, and scale-up of…
    • Compensation: CAD $60,000 – $90,000, commensurate with experience, qualifications, and relevant product development expertise.
    • We are seeking detail-oriented Medical Laboratory Technologists to perform clinical testing, quality control, and analyzer maintenance to ensure accurate and…
    • Attend all company-sponsored sales and medical meetings as directed by company management.
    • Foster collaboration with internal stakeholders, including marketing,…

  • Find better work in healthcare

    Explore helpful job resources with Careers in Care by IndeedExplore resources now
    • Preferred fields of study physical/athletic therapy, kinesiology, sports science or a related subject with knowledge of anatomy.
    • Training provided in Canada/US.
    • Responsible for achieving annual sales forecasts through professional implementation of approved sales and marketing materials.
    • Our group manages both academic grant funded and pharmaceutical/biotech funded studies, involving drugs and devices ranging across many disciplines: respiratory…
    • 3+ years of QA experience in biotech or medical device manufacturing.
    • Bachelor's degree in a technical discipline (e.g., engineering, biotech, pharmaceutical…
    • This role is a field-based 15-month contract and reports directly to the National Sales Manager, Oncology (Hematology).
    • Collaborating with scientific teams, preparing Animal Use Protocols (AUPs) and Standard Operating Procedures (SOPs), and overseeing day-to-day in vivo study…
  • View similar jobs with this employer
    • Helping manage our document management system (Veeva QualityDocs) by organizing files, updating records, and supporting team members with day-to-day questions.
    • You will be responsible for supporting our team's efforts in developing and executing toxicology studies to assess the safety of our drug candidates.
    • In this vital role, you will join the Predictive Biology team to develop and validate biologically relevant models of human tissue using induced pluripotent…
    • The successful candidate will lead and support cell surface target discovery, validation, and functionalization efforts by developing and applying innovative in…
Get email updates for the latest Medical Biotech jobs in Vancouver, BC

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

Career Resources:

Job Post Details

Quality Director, Pharmaceutical - job post

Filament Health Corp.
Burnaby, BC V5G 4X4•Hybrid work
$65,000–$70,000 a year - Temporary, Part-time, Fixed term contract

Job details

Pay

  • $65,000–$70,000 a year

Job type

  • Fixed term contract
  • Temporary
  • Part-time

Location

Burnaby, BC V5G 4X4•Hybrid work

Benefits

Pulled from the full job description

  • Paid time off
  • Work from home

Full job description

Job Overview

Filament Health is a small clinical-stage natural psychedelic drug development company. We are seeking a Part-Time Quality Director (remote) to provide oversight of GMP and regulatory quality activities over a 16-month contract term.

The ideal candidate will lead the development, implementation, and continuous improvement of quality management systems and provide ongoing support to the on-site Quality Manager. This role requires a strategic thinker with a strong understanding of Canadian and international guidelines for clinical trial drug manufacturing. The Quality Director will collaborate across departments to foster a culture of quality, compliance, and operational efficiency.

Key Responsibilities

  • Oversee all GMP programs and support the Quality Manager
  • Ensure all GMP documentation aligns with IMPDs and DMFs
  • Stay informed on changes in regulatory guidelines across multiple jurisdictions and ensure programs meet requirements
  • Lead third party audits including internal preparation and provision of documentation
  • Ongoing review and management of change control and CAPAs
  • Provide oversight of stability programs (protocols, schedules, reports)
  • Support EU regulatory activities, including RFI responses, regulatory requirement review, and IMPD updates
  • Act as the main QA contact for NNHPD, including renewal applications, RFIs, and ePLA submissions
  • Provide regulatory support for Health Canada and FDA, including DMF updates and RFI responses
  • Review and approve quality agreements

Qualifications

  • Senior-level experience in Quality within pharma or biotech
  • Experience managing people and cross-functional teams
  • Strong knowledge of drug development and regulatory submissions (IMPDs, DMFs, etc.)
  • Strong communication skills for reporting findings and collaborating across departments
  • Demonstrated expertise in QA processes and third party audits
  • Experience with botanical drugs an asset
  • Familiarity with EU, Health Canada, and FDA regulatory frameworks
  • Ability to work independently in a remote, part-time role
  • Ability to be on-site as needed
  • Proficiency with Google Workspace
  • Bachelor of Science (BSc), Microbiology, or Biochemistry
  • cGMP Compliance Training: HACCP, cGMP, SQF, regulatory compliance

Job Types: Part-time, Fixed term contract
Contract length: 16 months

Pay: $65,000.00-$70,000.00 per year

Expected hours: 20.0 – 25.0 per week

Benefits:

  • Paid time off
  • Work from home

Work Location: Hybrid remote in Burnaby, BC V5G 4X4

Let Employers Find YouUpload Your Resume