Production Specialist

2 days ago

Charlottetown, Prince Edward Island, Canada Next Level Group Full time
{"title": "Production Technician", "description": "Job Summary

We are seeking a highly skilled Production Technician to join our team at Next Level Group. As a key member of our production team, you will be responsible for ensuring the highest quality products are produced while maintaining a safe and efficient work environment.

Key Responsibilities
  • Adhere to the principles of safety first, quality always.
  • Perform sterile manipulations in both 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 procedures of clean rooms.
  • Responsibilities include cleaning, preparing, and sterilizing items in autoclaves.
  • Other duties as required.
Requirements
  • Biotechnology diploma would be an asset.
  • High School (Grade 12) diploma is a must.
  • 1-2 years of pharmaceutical/biological manufacturing experience in a 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, PowerPoint).
  • 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.
", "lang_code": "en-US"}

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