Production Technician

1 month ago

Charlottetown, Prince Edward Island, Canada Next Level Group Full time
Job Summary

We are seeking a highly skilled and detail-oriented Production Technician to join our team at Next Level Group. As a Production Technician, you will be responsible for performing a variety of tasks related to the production of biological products, including cell culture, viral infection processes, and quality control.

Key Responsibilities
  • Perform sterile manipulations in a biosafety hood and isolator
  • Maintain a cell line, completing media changes and cell passages
  • Operate and maintain production instruments and equipment, such as pH meters, conductivity meters, microscopes, lyophilized, peristaltic pumps, and other production equipment
  • Perform sterile cell culture and viral infection processes
  • Write and review batch records, SOPs, qualification documents for viral/Renogen operations
  • Complete timely SAP postings and maintain department inventory
  • Comply with safety requirements, cGMP, SOP, and manufacturing documentation
  • Collaborate with other departments involved in GMP manufacturing for planning production, testing, and product release in a timely manner resulting in successful completion of projects
  • Work as a cross-functional team with different manufacturing groups to provide resources as needed
  • Perform tasks under minimal supervision, and within tight timelines to meet production schedules
  • Assist in maintaining production equipment in good condition as per manufacturer's specifications
  • Maintain the cleanliness of the production areas and follow disinfection procedure of clean rooms
  • Responsibilities include cleaning, preparing, and sterilizing items in autoclaves
Requirements
  • Biotechnology diploma would be an asset
  • High School (Grade 12) diploma is a must
  • 1-2 years of pharmaceutical/biological manufacturing experience in GMP environment is preferred
  • 1-2 years of experience in aseptic techniques or cell culture experience is preferred
  • Excellent interpersonal skills, both communications and written
  • Outlines of Production, cGMP guidelines, and HSE regulations
  • Experience performing investigations and writing deviations
  • Intermediate/Expert computer skills using MS Office (Word, Excel, Power Point)
  • Thorough technical understanding of quality systems and regulatory requirements
Working Conditions
  • Must be able to work shift work (12-hour daytime shifts, 3-4 days/week including some weekends) and overtime as required
  • Required to assist in disinfection procedures involving hazardous chemicals requiring the use of a respirator
  • Must be able to lift, move, and maneuver small-medium sized equipment and raw materials – up to 50lbs
  • Requires ability to stand or sit for long periods of time
  • Requires frequent ladder or stair climbing
  • Must be able to read, write, understand, and comply with appropriate standard operating procedures

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