Stem Cell Processing Technician

5 years

0 Lacs

Posted:3 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description


Organisation:

Location:

Reports to:


1 Month TRAINING in PUNE



About ALIV

Autologous Cell Therapy



Role Summary


process PRP/PRFM




Key Responsibilities


Sample Handling & Chain of Custody


  • Receive, label, and track blood and bone-marrow aspirate; maintain time/temperature controls and transport logs.
  • Verify consent, requisitions, and kits; ensure traceability from collection to reinfusion.


PRP / PRFM Processing


  • Perform anticoagulation, centrifugation per protocol (soft/hard spins), plasma separation, platelet resuspension, PRFM activation.
  • Record volumes, spin parameters, platelet yield/concentration, and lot numbers of disposables.


Bone Marrow–Derived Cell Fraction Processing


  • Process aspirate using validated

    closed/open systems

    (e.g., RBC depletion, density separation).
  • Isolate mononuclear/cell fractions as per SOP; prepare final product for clinical use.


Asepsis, QC & Release


  • Work under

    Class II biosafety cabinet/laminar flow

    ; follow sterile technique and PPE.
  • Perform in-process QC:

    TNC/platelet counts, viability (e.g., Trypan Blue), recovery %, hemolysis check

    , appearance.
  • Prepare batch records and

    Certificate of Processing/Release

    for clinician sign-off.


Equipment & Facility


  • Operate and maintain

    centrifuges (fixed/swing), pipettes, cell counters/hemocytometer, vortex, incubators (if applicable)

    .
  • Daily/weekly

    calibration, IQ/OQ/PQ logs

    , maintenance tickets, and environmental hygiene records.


Compliance & Safety


  • Adhere to

    DCGI/ICMR guidance

    , clinic SOPs, biosafety, biomedical waste rules, and incident/AER reporting.
  • Participate in audits, CAPA, and periodic validation runs.


Inventory & Coordination


  • Manage stock of

    kits, anticoagulants, reagents, disposables

    ; raise purchase requests proactively.
  • Coordinate OR/clinic schedules for timely processing and delivery.




Qualifications


  • B.Sc./M.Sc.

    in Biotechnology/Microbiology/Biomedical/Allied Health

    or DMLT/BMLT

    .
  • 2–5 years

    in a cell/hematology/transfusion, IVF, orthobiologics, or day-care lab (PRP/BM processing preferred).
  • Strong grasp of aseptic technique, centrifugation theory, and basic hematology counts.
  • Comfortable with

    EMR/CRM/LIS

    , Google Workspace, and documentation discipline.
  • Languages:

    English + Hindi/Marathi (or local)

    .




Skills & Traits


  • Meticulous, steady hands, and

    SOP-first

    mindset.
  • Data-accurate; converts protocols into repeatable outputs.
  • Calm under time pressure; clear communication with clinicians and nursing.
  • Integrity, patient privacy, and teamwork.




KPIs


  • Yield & viability

    within spec;

    turnaround time

    adherence.
  • Documentation accuracy

    (batch records, logs) and SOP compliance.
  • Zero contamination/incident rate

    ; successful audits.
  • Stockouts avoided; equipment uptime.




90-Day Outcomes


  • 30 days:

    Trained and certified on ALIV SOPs; independent PRP runs with complete records.
  • 60 days:

    Independent bone-marrow fractionation; QC dashboards live.
  • 90 days:

    ≥95% runs within yield/viability specs; audit-ready documentation; proposes at least

    2

    process improvements.

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