Role & responsibilities
Maintains and documents proper records / log book / BPCRs / Reports as per GDP
Handling of Chromatography, sterilization & Filtration techniques.
Coordination with other department VIZ. engineering, QA, QC and R&D; for smoothly execution of Technical Documents.
Coordination with QA for timely issuance, completion, filling of BPCR and other GMP documents.
Preparation of Performance Verification and PQ and commissioning protocol Understanding & execution of work in line with cGMP.
Preparation of SOP, BPCR and other Technical Documents.
Handling of QMS Documents, Handling of DMS.
Execution of Training related activities of DSP area.
To ensure the timely dispensing of raw material and Handling of SAP.
To support in qualification activities of DSP area.
Execution of Process validation batches. Filling of all records,




Change Controls and QMS related Documents associated with DSP area.
Execution of IQ, OQ, PQ of equipments of downstream area.
Ensuring complete in-process quality control and continuous improvement in process capabilities. Investigating the OOS.OOT and handling process validation& cleaning validation. Plan and actively oversee team and shift activities to meet the production requirements

Job Type: Full time

Pay: ₹129,036.15 - ₹758,468.42 per year

Advantages:
Adaptable schedule
Food provided
Internet reimbursement
Leave encashment
Paid sick time
Provident Fund

Experience:
total work: 1 year (Preferred)

Work Location: In person

📌 Downstream Process Dsp Fresher/ Experience Manjusar (India)
🏢 Bills Biotech
📍 India