Senior Downstream Processing Technician
jfo_jfm_biopharmaceutical-manufacturing-operations-downstream-processing · S3 — S3 — Senior Support Specialist · Support
Experienced technician who independently executes complex downstream purification operations in biopharmaceutical manufacturing.
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Track
Support
Family rungs priced
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Coordinates
2 / 4 spaces
pay@2 · 2026-07
What this role is
Experienced technician who independently executes complex downstream purification operations in biopharmaceutical manufacturing. At the Senior Support Specialist (S3) level, the role owns escalated / complex cases, complex or non-standard cases, and drives resolution quality on the team's hardest cases. Guides junior support informally.
What this level does
- Run moderately complex downstream campaigns end-to-end using defined protocols, exercising judgment on sequencing, in-process timing and hold points with little day-to-day instruction
- Troubleshoot non-routine equipment and process issues (column packing quality, TFF flux decline, viral-filter integrity) during a run and decide whether to proceed, hold or escalate
- Draft deviation reports and initiate corrective/preventive action (CAPA) records for issues arising on the floor, and revise sections of batch records and SOPs for accuracy
- Coordinate the tasks of a suite crew across a run — assigning steps, sequencing equipment turnover and reviewing others' GDP entries — without holding formal supervisory authority
- Support qualification of downstream equipment by executing commissioning and requalification protocols
- Knowledge applied
- Detailed knowledge of downstream procedures sufficient to run moderately complex campaigns independently and to troubleshoot within defined protocols.
- Complexity & problem solving
- Makes judgments on moderately difficult in-process issues; decides proceed/hold/escalate and drafts deviations/CAPAs.
- Collaboration & interaction
- Coordinates suite tasks and reviews others' documentation; no formal leadership authority.
- Typical experience
- 2–4 yrs; skilled in downstream operations.
Skills at this level
- Purification unit operations
- — Sets up, operates and cleans chromatography systems, tangential-flow/UF-DF skids and viral filtration equipment to produce and polish bulk biologic drug substance.
- Buffer and media preparation
- — Weighs, mixes and QC-checks buffer and media solutions to specified recipes and stages them for downstream production runs.
- Good Documentation Practice (GDP)
- — Records batch parameters and completes/reviews batch records contemporaneously and accurately so downstream work meets Right-First-Time and data-integrity requirements.
- Batch record execution
- — Follows Master Batch Records and study protocols step-by-step to run downstream operations in a CGMP-compliant sequence with correct hold points and in-process checks.
- Cleanroom and 5S discipline
- — Maintains cleanroom facilities and downstream equipment in a controlled, organized state using 5S practices to preserve product and environmental integrity.
- Downstream equipment maintenance and troubleshooting
- — Performs preventive maintenance and diagnoses in-process faults on chromatography, filtration and mixing equipment (column packing, TFF flux, filter integrity) to keep runs on track.
- Raw material inventory control
- — Monitors, orders, receives and distributes downstream raw materials and consumables so scheduled runs are supplied without stockouts or expiry issues.
- Deviation and CAPA authoring
- — Investigates downstream floor deviations, documents root cause and writes corrective and preventive actions to prevent recurrence.
- SOP and MBR authoring
- — Writes and revises Standard Operating Procedures and Master Batch Records for downstream unit operations, translating process intent into executable GMP instructions.
- Equipment commissioning and qualification
- — Specifies, commissions and executes qualification/requalification protocols for new and existing downstream purification equipment.
- Process transfer
- — Transfers downstream processes between process development, the manufacturing floor, CMOs and partner sites, converting development conditions into qualified production procedures.
- Working lead coordination
- — Plans run readiness, sequences equipment turnover and assigns tasks across a downstream suite or shift, guiding and training less experienced associates without formal supervisory authority.
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https://jobframe.global/profile/jfo_jfm_biopharmaceutical-manufacturing-operations-downstream-processing%3A%3AS3
As of · 2026-07-30
Edition · canon-v2@2.1.0-complete
Source · canon-v2 cell + salary-benchmark (model)
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