Clean Room Assembler

Position Overview:
- Role Type: Contract (1 month, with potential for extension)
- Start Date: April 13
- Compensation: $23.00 per hour
- Schedule: 1st Shift 7:00 AM – 4:00 PM
- Workweek: 42.5 hours per week

Key Responsibilities:
- Compliance & Quality: Maintain strict adherence to Good Manufacturing Practices (GMP) and ensure all processes, documentation, and work areas comply with ISO13485 standards.
- Production Excellence: Optimize the use of labor, materials, and equipment to meet production specifications and budgeted costs.
- Inspections: Participate in receiving, in-process, and final inspections to ensure product integrity.
- Resource Management: Utilize ERP/MRP systems to schedule personnel and materials effectively.
- Equipment Maintenance: Ensure preventative maintenance is performed and equipment issues are resolved in accordance with the Quality Management System (QMS).
- Continuous Improvement: Drive improvements across people, processes, and equipment in alignment with company Quality Objectives.
- Facility Care: Maintain the cleanliness of the production area and manage all related documentation.

Position Requirements:
- Experience: Minimum of 5 years in a manufacturing environment (encompassing production, equipment, quality systems, and facility).
- Industry Knowledge: Previous experience working in a clean room environment and familiarity with the ISO13485 standard is required.
- Technical Skills: Extensive working knowledge of manufacturing and process equipment; proficiency in Microsoft Office (Outlook, Word, Excel) is a strong asset.
- Physical Skills: Excellent manual dexterity for handling delicate medical components.
- Communication: Proven ability to coordinate effectively with administrative, operations, quality, and engineering teams.
- Adaptability: Must be able to work a flexible schedule and lead continuous improvement efforts.

How to Apply:
If you are a quality-focused professional with the required experience in medical device manufacturing, we invite you to apply. Please submit your resume highlighting your experience with clean room protocols and ISO standards.

Advantages
- Work locally in Barrie
- Opportunity for a long-term career
- Build your experience in a clean room

Responsibilities
- Compliance & Quality: Maintain strict adherence to Good Manufacturing Practices (GMP) and ensure all processes, documentation, and work areas comply with ISO13485 standards.
- Production Excellence: Optimize the use of labor, materials, and equipment to meet production specifications and budgeted costs.
- Inspections: Participate in receiving, in-process, and final inspections to ensure product integrity.
- Resource Management: Utilize ERP/MRP systems to schedule personnel and materials effectively.
- Equipment Maintenance: Ensure preventative maintenance is performed and equipment issues are resolved in accordance with the Quality Management System (QMS).
- Continuous Improvement: Drive improvements across people, processes, and equipment in alignment with company Quality Objectives.
- Facility Care: Maintain the cleanliness of the production area and manage all related documentation.

Qualifications
- Experience: Minimum of 5 years in a manufacturing environment (encompassing production, equipment, quality systems, and facility).
- Industry Knowledge: Previous experience working in a clean room environment and familiarity with the ISO13485 standard is required.
- Technical Skills: Extensive working knowledge of manufacturing and process equipment; proficiency in Microsoft Office (Outlook, Word, Excel) is a strong asset.
- Physical Skills: Excellent manual dexterity for handling delicate medical components.
- Communication: Proven ability to coordinate effectively with administrative, operations, quality, and engineering teams.
- Adaptability: Must be able to work a flexible schedule and lead continuous improvement efforts.

Summary
We are looking for a highly skilled and detail-oriented Clean Room Operator to join our production team. This role is critical in ensuring our medical device manufacturing processes meet the highest standards of quality and efficiency. You will be responsible for utilizing resources effectively to produce products that exceed customer expectations while adhering to strict ISO13485 and GMP standards.

If you are a quality-focused professional with the required experience in medical device manufacturing, we invite you to apply. Please submit your resume highlighting your experience with clean room protocols and ISO standards.


Randstad Canada is committed to fostering a workforce reflective of all peoples of Canada. As a result, we are committed to developing and implementing strategies to increase the equity, diversity and inclusion within the workplace by examining our internal policies, practices, and systems throughout the entire lifecycle of our workforce, including its recruitment, retention and advancement for all employees. In addition to our deep commitment to respecting human rights, we are dedicated to positive actions to affect change to ensure everyone has full participation in the workforce free from any barriers, systemic or otherwise, especially equity-seeking groups who are usually underrepresented in Canada's workforce, including those who identify as women or non-binary/gender non-conforming; Indigenous or Aboriginal Peoples; persons with disabilities (visible or invisible) and; members of visible minorities, racialized groups and the LGBTQ2+ community.

Randstad Canada is committed to creating and maintaining an inclusive and accessible workplace for all its candidates and employees by supporting their accessibility and accommodation needs throughout the employment lifecycle. We ask that all job applications please identify any accommodation requirements by sending an email to accessibility@randstad.ca to ensure their ability to fully participate in the interview process.

This posting is for existing and upcoming vacancies.