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Manufacturing Technician II at client Oceanside - JobAssist
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Home›Jobs›IT & Software›Manufacturing Technician II
client Oceanside logo

Manufacturing Technician II

client Oceanside

RemoteFull timeMid levelPosted today
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About the role

About This Role

The Manufacturing Technician II executes manufacturing processes, rigorously following batch records, SOPs, and cGMP regulations to ensure safe and compliant operations. This role is a contract position that involves working as part of a team to perform GMP runs in close collaboration with various departments.

Responsibilities

  • Execute manufacturing processes on the floor under supervision, while rigorously following batch records, standard operating procedures (SOPs), and Current Good Manufacturing Practice (cGMP) regulations to ensure manufacturing operations are safe and compliant
  • Ensure right-the-first-time performance of all process steps specific to the phase or stage of operation, as well as help drive the safety-first culture at client Oceanside
  • Work as part of a team to execute Good Manufacturing Practice (GMP) runs in close collaboration with Manufacturing Science and Technology (MSAT), Facilities and Engineering (F&E), and Quality departments
  • Under supervision, perform weighing of raw materials, as well as electronic inventory transactions utilizing Manufacturing Execution Systems (MES) and Enterprise Business system (EBS)
  • Under supervision, perform cell culture and filling unit operations for the manufacturing of viral vector products in a cGMP environment using proper aseptic technique, proper laboratory etiquette, Good Documentation Practices (GDP), and sound scientific methods
  • Prepare and use single-use systems to support solution formulation and filter integrity testing
  • Maintain mammalian cell culture in flasks, CellSTACK chambers, and single-use bioreactor systems
  • Assist with transfection of cells and harvest of viral vectors
  • Assist with manual and/or automated fill of harvested viral vector material
  • Escalate processing and equipment issues as needed
  • Assist with revisions of SOPs, Manufacturing Production Record (MPRs), and other controlled documents
  • Assist in the review of in-process cGMP documentation for completeness, accuracy, and compliance
  • Work effectively in an inclusive, cross-functional, team-based environment
  • Work off-shift hours and weekends
  • Perform additional duties as assigned

Important Details

  • Duration: 12 months with possible extension

Job details

Workplace

Remote

Employment

Full time

Seniority

Mid level

Headquarters

Oceanside, CA

Posted

Posted today

About company

Unicon Pharma provides customized workforce solutions for life sciences companies, bringing innovative treatments from concept to reality.

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Headquarters

Oceanside, CA

Open jobs

1

Website

uniconpharma.com
client Oceanside logoclient Oceanside