Promea Therapeutics Jobs | Production, QA, QC & Bioanalytical Careers
byAkshay Badakh—0
Promea Therapeutics Jobs – Pharma Manufacturing, QA & QC Careers
Promea Therapeutics Pvt. Ltd. is conducting a walk-in drive for freshers and experienced professionals at its Medical Devices Park facility in Sultanpur, Ameenpur, Sangareddy, Telangana. Openings are available in Production, Biologics, Bioanalytical, Cell & CAR-T Laboratories, QA and QC-Microbiology departments. The advertised positions are for male candidates only.
Coordinate with QA, QC, Engineering, and Production teams.
2) Department: LVP Production
Designation: LVP Production – Jr Executive
No. of Positions: 10
Experience: Freshers
Qualification: B.Sc / M.Sc (Chemistry / Biotechnology), B Pharmacy / M Pharmacy / B Tech / M Tech Biotechnology
Key Skill or Job Description:
Batch calculation and Dispensing
CIP and SIP activities & Filter integrity test
Batch preparation as per cGMP and GDP
Material reconciliation & Men and Material movement
Knowledge on Calibration and validation activities
3) Department: Biologics Production
Designation: Biologics Production – Jr Executive
No. of Positions: 10
Experience: Freshers
Qualification: B.Sc / M.Sc (Chemistry / Biotechnology), B Pharmacy / M Pharmacy / B Tech / M Tech Biotechnology
Key Skill or Job Description:
Responsible for Downstream Plasma Process
Responsible for Buffer preparation
Responsible for handling pH meter, Spectrophotometer and Conductivity meter
Responsible for performing Depth filtration
Responsible for Protein purification (TFF)
4) Department: Bioanalytical
Designation: Sr. Analyst / Sr. Research Associate
Experience: 2–6 Years
Qualification: B.Pharm / M.Pharm
Key Skill or Job Description:
Perform sample preparation, solution preparation, routine bioanalytical testing, and data review in compliance with SOPs, GLP, and regulatory guidelines.
Develop and validate LC-MS/MS bioanalytical methods, including literature review and method optimization.
Prepare and review SOPs, analytical methods, project plans, protocols, and validation documentation.
Operate and maintain LC-MS/MS instruments for method development, validation, and study sample analysis while ensuring data quality and compliance.
5) Department: Cell & CAR-T Laboratories – QC
Designation: Executive / Sr Executive
Experience: 2–4 Years
Qualification: B.Sc / M.Sc
Key Skill or Job Description:
Perform Cell Culture QC testing for cell therapy products, raw materials, and in-process samples.
Execute cell-based assays including Flow Cytometry, Viability, Cytotoxicity, Endotoxin, and Mycoplasma testing.
Review analytical data and maintain GMP, GLP, and Data Integrity compliance.
Support method validation, assay qualification, investigations (OOS/OOT/CAPA), and documentation.
Ensure practices, laboratory compliance, and instrument qualification.
Coordinate with Manufacturing, QA, and Microbiology teams for batch release activities.
6) Department: QA
Designation: Executive / Sr Executive
Experience: 2–8 Years
Qualification: B.Pharm / M.Pharm / M.Sc
Key Skill or Job Description:
Execute QA, IPQA, Validation, QMS & AQA activities as per GMP and regulatory requirements.
Perform IPQA checks, line clearances, batch document review and in-process compliance monitoring.
Support qualification/validation, deviations, CAPA, change controls, OOS/OOT and investigations activities.
Maintain SOPs, audit protocols and data integrity as per Quality system compliance.
7) Department: QC – Microbiology
Designation: Executive / Sr Executive
Experience: 1–6 Years
Qualification: B.Pharm / M.Sc / M.Sc Microbiology
Key Skill or Job Description:
Perform testing of Raw Materials, In Process, Finished Products & Stability samples as per STPs.
Operate HPLC, GC, UV, FTIR, Dissolution and other QC instruments.
Prepare reagents, standards, mobile phases & test solutions.
Support stability, method validation/transfer/OOS/OOT, deviations & CAPA activities.
Ensure compliance with GMP, GLP, CGP, AIC and laboratory safety.
Perform Microbiological testing of raw materials, water, in-process and finished products, including MLT, BET, sterility and environmental monitoring as applicable.
Maintain cGMP/GLP compliance, prepare reagents/media, operate microbiology instruments and ensure accurate documentation & data integrity.
Walk-In Interview Details for Freshers
Walk-In Interview Date: 14 August 2026 (Friday)
Time: 09:00 AM to 03:00 PM
Venue: Promea Therapeutics Pvt. Ltd., Medical Devices Park, Sultanpur, Ameenpur, Sangareddy, Telangana – 502319
Candidates should carry:
Updated Resume
Photograph
Educational Certificates
Walk-In Interview Details for Experienced Candidates
Walk-In Interview Date: 14 August 2026 (Friday)
Time: 09:30 AM to 01:00 PM
Venue: Promea Therapeutics Pvt. Ltd., Medical Devices Park, Sultanpur, Ameenpur, Sangareddy, Telangana – 502319
Candidates should carry:
Updated Resume
Photographs
Educational Certificates
Latest Increment / CTC Details
Frequently Asked Questions
1) Is the Promea Therapeutics walk-in interview open for freshers?
Yes. Promea Therapeutics has advertised separate fresher positions in LVP FFS Operations, LVP Production and Biologics Production.
2) What qualifications are accepted for the fresher positions?
The fresher vacancies accept qualifications including ITI, Diploma in Mechanical/Electrical, B.Sc., M.Sc., B.Pharm, M.Pharm, B.Tech and M.Tech Biotechnology, depending on the position.
3) What experienced positions are available at Promea Therapeutics?
Experienced openings are available in Bioanalytical, Cell & CAR-T Laboratories – QC, QA and QC-Microbiology.
Promea Therapeutics Walk-In Interview for Freshers and Experienced Pharma Professionals
Promea Therapeutics jobs for Production QA QC Bioanalytical and Biologics professionals
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