Cell Processing Specialist

Job Description: Cell Processing — PRP & Bone Marrow–Derived Cell Fractions

Organisation:

ALIV Regenerative Wellness Location:

Pune |

Type:

Full-time |

Mode:

On-site Reports to:

Lab/Clinical Operations Lead

1 Month TRAINING in PUNE

About ALIV ALIV is a compliant regenerative wellness clinic focused on

Autologous Cell Therapy ,

PRP/PRFM , and

targeted IV therapies , delivered with strict ethics and SOPs.

Role Summary

Hands-on technician to

process PRP/PRFM

and

bone marrow–derived autologous cell fractions (minimally manipulated)

with impeccable aseptic technique, documentation, and turnaround time. You’ll partner with clinicians to ensure safe, consistent, and reproducible outputs for patient procedures.

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.