ABOUT US:

We pride ourselves on fostering a positive work culture that cultivates innovation, collaboration, and employee well-being. Our team is a close-knit group of passionate individuals who share a common dedication to advancing scientific discovery and improving the lives of those around us. Open communication is a cornerstone of our culture, with regular team meetings, brainstorming sessions, and an approachable leadership team that encourages feedback and ideas from all levels. Our commitment to professional development ensures that team members have the resources and opportunities to grow in their careers. The result is a dynamic and supportive work environment where every team member feels valued, motivated, and empowered to contribute their best to the exciting field of biotechnology.

JOB DESCRIPTION:

Reporting to the Quality Supervisor, the successful candidate will be responsible for maintaining quality control standards by inspecting, testing and approving of incoming raw materials, reagent formulations, reagent biologicals, in-process sub-assemblies and finished products.

QUALIFICATIONS:

• Bachelor of Science (BSc) in a microbiology discipline preferred.
• Working experience in an ISO and GMP compliant environment, and knowledge in ISO13485.
• Minimum 2-3 years experience working in a Quality Control microbiology laboratory.

EDUCATION:

• Bachelor of Science Degree (BSc) in Biology, Microbiology, or related discipline required from a recognized university.
  Job Types: Full-time, Permanent
  Pay: $45,000.00-$50,000.00 per year

Benefits:

• Casual dress
• On-site parking

Education:

• Bachelor’s Degree (required)

Experience:

• relevant: 2 years (required)

Work Location: In perso

• Inspection and approval of incoming raw materials.
• Approval and reconciliation of labels.
• Perform microbiological testing of in-process and finished products.
• Conduct tests for bioburden, stability and validation samples.
• Cleaning and sanitization of work areas.
• Create, revise, review and/or approve control documents including standard operating procedures, manufacturing instructions, book of methods, material specifications, and reagent formulations.
• Participate in Raw Material Qualification, Stability Validation and Equipment Validation
• Participate in nonconformance investigations.
• Investigate customer complaints and inquiries.
• Daily monitoring of temperature of refrigerators, incubators and equipment.
• Documentation review including batch records, equipment maintenance and calibration records, cleaning and sanitization checks and etc.
• Calibration of Pipettes
• Maintenance of bacteria culture collection.
• Preparation of culture media.
• Create Certificates of Analyses.
• Perform all work in a safe manner and maintain a clean and organized work environment
• Perform related tasks as assigned.