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Product Development Specialist

NGARE EMPLOYMENT SOLUTIONS PTY LTD

Ontario

On-site

CAD 65,000 - 80,000

Full time

5 days ago
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Job summary

A leading company in the Cannabis industry is seeking an NPC Development Specialist in Barrie, Ontario. The role involves technical writing, product development, and process optimization in a collaborative environment. This 6-month contract offers opportunities for extension.

Qualifications

  • Minimum of 2 years of relevant experience is an asset.

Responsibilities

  • Plan and execute product and technology processes.
  • Draft research protocols and technical documents.
  • Coordinate project timelines across functions.

Skills

Scientific and Technical Writing
Project Management
Communication
Organizational Skills
Multi-tasking

Education

BSc in Health Sciences
Bachelor of Engineering

Tools

Microsoft Office

Job description

Located in Barrie, Ontario, MediPharm Labs offers a professional and collaborative workplace culture in a leading-edge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry. Our growing team of scientists, technicians, engineers, and business professionals delivers quality and innovation through research, discipline, and forward thinking.

POSITION SUMMARY :

The NPC Development Specialist will be involved in technical writing, development of new products and processes, and improving / optimizing existing processes. The successful candidate will provide a high level of technical expertise and actively participate with other staff to complete projects and production tasks in an effective and timely manner.

6 Month contract with opportunity for extension

ROLE SPECIFIC RESPONSIBILITIES :

  • Plan and execute product, new technology processes and business development execution projects.
  • Coordinate across all functions and be accountable to deliver project timelines.
  • Define project scope, goals, and deliverables and gain acceptance from stakeholders and executive team.
  • Assist with, and when appropriate lead, projects focused on product development and process improvement.
  • Draft research protocols and reports, standard operating procedures, batch work instructions, and other technical documents.
  • Work with third-party consultants and equipment suppliers as required.
  • As required, coordinate required maintenance, calibration, and qualification of instruments.
  • Other related duties as assigned.

Required Skills :

  • Expertise in scientific and technical writing is required.
  • Ability to manage and execute multiple projects concurrently is required.
  • Must be a self-motivated, creative individual able to work in a team environment.
  • Knowledge of regulations and / or experience working in a regulated environment such as GPP or GMP is an asset.
  • Strong communication, organizational, and multi-tasking skills.
  • Knowledge of Microsoft Office, including Excel and Word.
  • Ability to estimate, budget, and schedule all elements of project management.
  • Strong communication skills, both verbal and written, ability to communicate and adjust to different internal and external audiences using various media.

Required Qualifications :

  • Minimum of BSc or Bachelor of Engineering in Health Sciences.
  • At least 2 years of relevant experience is an asset.

To apply online, please click on the appropriate link below.

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