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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required for Production DPM & DSP- M.Sc Biotechnology /Biochemistry / Chemistry

Hetero Pharma is looking for talented professionals with 2-5 years of experience in Biopharma Production Operations. Hetero Plasma Sciences is hiring for Production DPM & DSP 1. Location: Penjerla Village, Kothur Mandal, Rangareddy, Telangana 2. Department: Production - DPM 3. Experience in: -Aseptic Production -CIP/SIP Operations -GMP Documentation -Sterile Manufacturing Equipment Handling 5. Department: Production - DSP Qualification: M.Sc Biotechnology /Biochemistry / Chemistry Experience in: -Protein Purification -Chromatography -UFDF -Filtration & Centrifugation GMP Documentation -DSP Operations 6. How to Apply:  Interested candidates can share their CVs to: maniteja.s@hetero.com Click Here for Details
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Required QA-Microbiologist (Sterile)

Emcure Pharmaceuticals is hiring QA  Microbiologist for Pune Location 
Details are provided below 
1. Position: QA-Microbiologist (Sterile)
2. Location: Pune 
3. Experience: 2-5 Years
4. Role: 
-Review, verify, and approve microbiological documents and reports, including Sterility, BЕТ, Bioburden, GPT, MLT, environmental monitoring, water testing, Vitek-2/MS data, logbooks, and electronic records.
-Review and approve microbial test reports, environmental monitoring data, validation, qualification, and study protocols/reports.
-Handle QMS documentation: Notifications, excursions, deviations, investigations, OOS/OOT, trend analysis, and summary reports.
-Manage document control lifecycle-issuance, control, retrieval, retention, and destruction of SOPs, specifications, formats, logbooks, validation protocols, BMRs, BPRs, and finished product reports.
-Ensure and witness critical microbiology activities such as media plate release, media fill visual inspection, plate reconciliation, and issuance verification.
-Review completeness and compliance of media preparation, GPT, biological testing, and other supporting records.
-Monitor manufacturing, processing, and packaging operations to ensure cGMP, GLP, and GDP compliance, with authority to stop operations if required.
-Participate in process validation, cleaning validation, media fills, stability management, and management reviews.
-Initiate, issue, and support QMS documents and departmental SOPs in line with regulatory guidance.
-Ensure training compliance, adherence to safety, data integrity, ethical conduct policies, and timely escalation of quality or DI risks.
-Maintain effective communication and escalation of quality issues to QA leadership.
5. Experience: 
2-5 years of experience in sterile QA-Microbiology only
Strong understanding of cGMP and QMS systems
Sharp documentation skills with a positive, quality-first mindset
A team spirit and enthusiasm to learn and grow
6. How to Apply: 
 Share your CV on Amrutar.paturde@emcure.com

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