S1
jfo_jfm_manufacturing-operations-bioprocess-manufacturing-upstream-d::S1
Bioprocess Manufacturing Technician
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Bioprocess Manufacturing Technician

jfo_jfm_manufacturing-operations-bioprocess-manufacturing-upstream-d · S1 — S1 — Support Associate · Support

Entry-level individual contributor supporting upstream and downstream bioprocess manufacturing operations under close supervision.

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Support

Family rungs priced

Coordinates

2 / 4 spaces

pay@2 · 2026-07

What this role is

Entry-level individual contributor supporting upstream and downstream bioprocess manufacturing operations under close supervision. At the Support Associate (S1) level, the role owns a single task type or queue, routine, well-defined requests, and drives individual transactions. None.

What this level does

  • Weigh and check raw materials and consumables against the batch record, following specific step-by-step instructions for a single assigned unit operation (e.g., media weigh-out or glass wash)
  • Assemble, clean and sterilize process equipment, performing clean-in-place (CIP) and sterilize-in-place (SIP) steps exactly as written in the SOP
  • Complete entries in electronic work instructions and Batch Production Records at the time of the task, following Good Documentation Practices under close review
  • Maintain the clean room environment — gowning, line clearance and housekeeping — to the prescribed cGMP standard for the assigned area
Knowledge applied
General knowledge of upstream cGMP routines — gowning, weigh-out, CIP/SIP and documentation — applied to prescribed tasks with answers readily available in the SOP.
Complexity & problem solving
Routine, single-step tasks; problems have a known answer and are referred up rather than judged.
Collaboration & interaction
Completes own assigned tasks; standard interaction with shift peers and lead.
Typical experience
0–1 years; minimal experience.

Skills at this level

Aseptic technique
Performs sterile manipulation of cell culture during transfers, sampling and inoculation, working within a Grade A environment to prevent contamination of the culture.
Media preparation
Prepares and sterilizes cell-culture media from stage-specific recipes, weighing and dispensing ingredients for each phase of the growth and production process.
Bioreactor operation
Operates seed-train and production bioreactors from bench to production scale, controlling temperature, pH, dissolved oxygen and feed additions across batch and fed-batch culture modes.
CIP/SIP and equipment sterilization
Assembles, cleans and sterilizes process equipment by executing clean-in-place and sterilize-in-place cycles per SOP, and verifies the equipment is ready for aseptic use.
Batch record execution
Executes and documents Batch Production Records for upstream unit operations in real time, capturing weigh-outs, setpoints and in-process readings under Good Documentation Practices.
GMP and regulatory compliance
Applies cGMP regulations and company SOPs to upstream manufacturing, maintaining clean-room controls and records that satisfy regulatory requirements.
In-process monitoring
Monitors culture parameters during runs, recognizes drifts or excursions in pH, DO and temperature, and takes or escalates the correct procedural response.
Deviation and CAPA support
Reconstructs floor-level events during deviation investigations and proposes corrective/preventive actions to stop process or equipment problems recurring.
Procedure authoring and training
Drafts and qualifies new upstream SOPs, batch record templates and aseptic procedures, then trains and coaches operators on their correct execution.
Working lead / task coordination
Coordinates equipment turnaround and shift task sequencing across the upstream suite and directs and verifies the work of less experienced associates without formal supervisory authority.
Teamwork and communication
Collaborates on shift work teams and with QA, MSAT and engineering, communicating in-process status and handoffs where combined contribution and results are expected.

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As of · 2026-07-31

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