Who We Are

Response Biomedical Corp. has been transforming acute care diagnostic testing, with a 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 total cost of care.

Who we are looking for?

We are seeking for a dynamic Quality Control Lead who is self-motivated and enjoys working in a fast paced environment. This position is responsiblefor overseeing the daily QC activities within the organization, ensuring that all raw materials, components, and finished products undergo rigorous inspection and testing to meet established quality standards.The Quality Control Lead is also responsible for providing technical expertise on QC practices, optimizing processes, and contributing to continuous improvement initiatives., for the core purpose of improving patient outcomes and saving lives globally.

Key Responsibilities

QC Planning and Scheduling

Provide key information to allocate QC resources effectively for smooth workflow.
Assist in scheduling and organizing QC activities to meet targets.
Coordinate with Planning, Production, Facilities, and Quality Assurance to ensure timely product completion.
Facilitate interdepartmental communication for prompt decision-making.

Quality Control Activities

Oversee daily QC operations, providing technical guidance and direction.
Execute complex QC testing and material inspection, adhering to SOPs and batch records.
Maintain and update test procedures for products and raw materials.
Review QC documents for accuracy and completeness.
Perform laboratory housekeeping.
Act as a technical expert for QC practices.

Scientific and Technical Support

Train QC Specialists and provide technical guidance to Manufacturing and QA teams to ensure optimal process performance.
Support investigations, root cause analyses, and complaint handling.
Develop and maintain test procedures, including stability programs.

Quality Systems

Adhere to and enforce compliance with Quality Management System (QMS), GMP, GDP, ISO, and safety regulations.
Report quality and equipment issues to the QC Manager.
Perform QVB and in-process inspections during manufacturing, and complete transactions in the ERP system for inventory management.
Ensure accurate and timely completion of regulatory documentation.
Support CAPAs, VRs, OOS and NCs, and improve GMP and QMS.

Process Optimization

Collaborate with the QC Manager to troubleshoot issues and implement process improvements.
Continuously evaluate and improve QC efficiency, reducing waste.

Inventory Management

Oversee QC inventory and equipment for availability and functionality.
Support inventory counts and resolve discrepancies.

Health and Safety

Follow and enforce safety protocols to maintain a compliant and safe work environment.
Ensure that QC areas are kept clean and organized.

Formal Education

Education, Work Experience, Knowledge, and Skills:

Post-secondary degree in Chemistry, Biology, Biochemistry, or related fields.
Occupation First Aid level 1 or higher is an asset.
Lean Six Sigma certification (Green Belt) is an asset.

Work Experience

3+ years in QC process, ISO standards, and regulated environments.
3+ years in lab settings, preferably with medical devices or related fields.
Supervisory / project management roles experience is an asset.

Skills And Knowledge

Proven ability to effectively train and mentor QC staff, ensuring skill development and fostering team engagement.
Strong professional and technical knowledge in QC processes, with a deep understanding of operational requirements.
Expertise in regulated environments and quality standards (ISO 13485, GMP, GDP, etc.).
A strong commitment to maintaining workplace safety and ensuring compliance with all relevant safety protocols.
Ability to quickly adapt to changing priorities and manage multiple tasks simultaneously in a dynamic production environment.
Strong capability to plan, organize, develop, and implement business communications, policies, procedures, and ensure compliance with governmental regulations.
Excellent organizational, interpersonal, and communication abilities, ensuring clear collaboration across teams.
Proficient in Microsoft Office Suite, particularly Word and Excel, with experience in ERP systems for QC data input and management.
Excellent problem-solving, communication, and scientific writing abilities.
Exhibits personal values that strongly align with the company’s vision, values, and culture, contributing to a positive team environment.

The starting salary for this position ranges from $68,000 to $74,000 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.

Response Biomedical Corp.

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