Product Development Scientist

at  Response Biomedical

WHO WE ARE:

Response Biomedical Corp. has been transforming acute care diagnostic testing, with the central focus on improving patient outcomes and healthcare reform for over 20 years. Response Biomedical fosters a values-based culture, committed to making diversity and inclusion our way of doing business. We believe the people we work with including our partners, medical teams, and employees are the cornerstone of our success.
What we do:
Our RAMP platform is a global leader in diagnostic testing solutions for use in cardiovascular, infectious disease, sepsis, women’s health, arbovirus, and biodefense. We understand the stresses associated with rapid, accurate diagnosis when every minute counts, and are committed to collaborating with the teams that are dedicated to saving lives. We do this by providing lab-quality results within minutes that medical teams can trust while reducing the total cost of care.

WHO WE ARE LOOKING FOR:

We are seeking a motivated, dynamic, solutions-focused, and creative individual to join our Product Development Team. This position will assist in the leading the design, development, and execution of original scientific research, applied technology, and/or development projects to support the improvement and expanded application of Response Biomedical product technologies with the understanding that these products are used in the aid in diagnosis of potentially life-threatening diseases.

FORMAL EDUCATION:

Minimum requirements: M. Sc. or an equivalent combination of relevant education (post secondary education in Biochemistry, Biology, Medical Technology, or Related Science.) and work experience.

WORK EXPERIENCE:

• 5 years relevant work experience or equivalent combination of education and experience
• At least 3 years of laboratory experience is required.
• Previous experience in a medical device or pharmaceutical development environment is an asset.

SKILLS AND KNOWLEDGE:

• Strong scientific writing skills and experience creating and reviewing technical documentation. Excellent written and verbal communication skills.
• Experience related to medical devices, protein biochemistry, and immunological methods.
• High level of proficiency with Microsoft Office productivity suite and database applications.
• Strong problem identification and problem resolution skills.
• Knowledge of requirements working in a regulated environment under the guidelines set by the Company to assure compliance with the Medical Device Single Audit (MDSAP) regulations, ISO13485, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Design Control and Workers Safety.
  The starting salary for this position ranges from $65,000 to $75,000 annually, depending on the candidate’s experience and qualifications. Our salary structure is aligned with market standards and is finalized considering factors such as job-related expertise, skills, education, and experience.

Please note that this position is only available to candidates who are authorized to work in Canada.

• We regret that relocation will not be provided.
• While we appreciate the interest of all applicants, only those candidates selected for interview will be contacted.

We’re committed to a diverse and inclusive workplace. We welcome applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. All employment decisions are based on business needs, job requirements and individual qualifications.