Bionik is building a dynamic team to develop new transformational technologies and solutions for individuals with neurological disorders. We are seeking highly motivated individuals who enjoy working in a high paced, collaborative and goal-oriented environment. Bionik is an equal opportunity employer offering competitive compensation, employee benefits and the opportunity for personal and professional growth in an outstanding and intellectually challenging work environment.

Please contact us at hr@bioniklabs.com for further information or to submit your resume.

Openings

Join Bionik, and become part of a dynamic team that develops solutions for individuals with neurological disorders and mobility challenges. We are seeking highly motivated individuals who enjoy working in a fast paced, collaborative and goal-oriented environment.

Bionik Laboratories is a global, pioneering robotics company focused on providing rehabilitation solutions to individuals with neurological disorders. Through the recent acquisition of Interactive Motion Technologies, Bionik has added a portfolio of products focused on upper and lower extremity rehabilitation of stroke patients. The Company now has three products available on the market and is driving development on its next set of new platform products.

Position Description:

The Software Engineer will specialize in implementing the software ecosystem, including the design and documentation in a medical robotics environment. This position is responsible for the design, development, documentation, improvements and maintenance of the IT infrastructure and processes in a regulated environment.

Location: Toronto, Ontario, Canada

Reports to: Strategic Project Leader

Qualifications:

  • Bachelor’s Degree in Computer Science
  • 5+ years experience, preferably in regulated environments (ie IEC62304)
  • Passionate about robotics

Required Knowledge / Experience:

  • Experience implementing and maintaining IT infrastructure
  • Strong documentation skills
  • Server & network, databases, APIs, UI & UX, HTML5, Javascript, CSS3, C, Unix-like
  • Systems thinker
  • Experience with Full Stack Development
  • Ability to understand and interpret the business needs/environment
  • Ability to work collaboratively with a multi-disciplinary team
  • Big picture perspective
  • Self-directed

Preferable:

  • Previous experience in a Quality Management System an asset
  • Experience with HIPPA & HL7

 

Ability to work in multi-cultural environments and travel internationally as required to support business needs.

 

Perks:

  • Competitive compensation
  • Employee benefits (medical, dental & health spending account)
  • Matching RRSP program
  • Intellectually challenging work environment
  • Great downtown location!

If this sounds like your future, please apply at hr@bioniklabs.com with your cover letter and resume.

Job Position: Quality Specialist

Join Bionik, and become part of a dynamic team that develops solutions for individuals with neurological disorders and mobility challenges. We are seeking highly motivated individuals who enjoy working in a fast paced, collaborative and goal-oriented environment.

Bionik Laboratories is a global, pioneering robotics company focused on providing rehabilitation solutions to individuals with neurological disorders. Through the recent acquisition of Interactive Motion Technologies, Bionik has added a portfolio of products focused on upper and lower extremity rehabilitation of stroke patients. The Company now has three products available on the market and is driving development on its next set of new platform products.

Position Description:

The Quality Specialist is responsible for providing support in all areas of Bionik’s’ Quality Management System, including:

  • CAPA, Training, Doc Control, Complaints, MRB, Internal Audits, Management Reviews, Customer Complaints, and Customer Support.
  • Managing the documentation required as part of the Quality System related to Manufacturing
  • Assisting in the maintenance of supplier certification/performance measurement program data
  • Receiving and Inspection of incoming materials
  • Assisting in manufacturing processes and driving product quality
  • Other duties as required

Reports to: Director QA/RA

Qualifications:

  • Bachelor’s Degree in Science or Engineering (or related field).
  • 3 to 5 years relevant work experience in a medical device environment

 

Required Knowledge / Experience:

  • Proven track record, must be organized, able to meet deadlines, and have a strong attention to detail
  • Knowledge of FDA Quality System Regulation (21 CFR 820), ISO 13485, Medical Device Directive 93/42/EEC
  • Knowledge of ISO 14971 – Application of risk management to medical devices.
  • Self-starter, able to work independently with the ability to manage multiple priorities
  • Analytical thinker with strong problem solving skills
  • Capable of streamlining, improving processes and troubleshooting.
  • Solid communication skills; both verbal and written
  • Bachelor’s in Science Degree or equivalent
  • Experience in supplier relations
  • Familiar with product specifications and incoming inspection procedures
  • Experience in a GMP/medical device environment with ISO 13485, FDA, Medical Device Directive 93/42/EEC
  • Strong knowledge of MS Office and experience with customizing spreadsheets

 

Perks:

  • Competitive compensation
  • Employee benefits (health, medical, dental and Flexible Spending Account)
  • Intellectually challenging work environment
  • Great greater Boston location!

If this sounds like your future, please apply at hr@bioniklabs.com with your cover letter and resume.

Bionik Laboratories is an equal opportunity employer and welcomes & encourages applications from people with disabilities. Accommodations are available on request for candidates participating in the recruitment process.

We thank all applicants for their interest, however only those best suited to our current needs will be contacted.