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

Required Sr. Officer / Executive - Upstream Fermentation, Executive/ Senior Executive - Water System & HVAC , Effluent Treatment Plant (ETP) Chemist and Quality Control Reviewer

CONCORD BIOTECH is hiring for multiple positions  Details are provided below  1. Position : Sr. Officer / Executive - Upstream Fermentation  2. Experience: 05 to 12 Yrs Exp 3. Job Responsibilities:  -Execute upstream fermentation operations as per SOP and cGMP guidelines. -Perform media preparation, inoculum preparation, sterilization, and culture transfer activities. -Operate and monitor bioreactors/fermenters during batch and fed-batch processes. -Monitor process parameters like pH, DO, temperature, agitation, airflow, and pressure. -Perform CIP/SIP activities and ensure equipment cleanliness and sterility. -Maintain aseptic conditions during all fermentation operations. -Conduct routine sampling and process monitoring activities. -Handle fermentation-related documentation, logbooks, and batch manufacturing records. -Identify and troubleshoot process abnormatities during fermentation. -Coordinate with QA, QC, Engineering, and Maintenance departments. -F...
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Required Study Director - Toxicology-GLP3. Qualification: PhD/M.VSC / M.Pharm / MSc in Toxicology, Pharmacology, Life Sciences

Aragen Biosafety Solutions Pune is hiring for Study director.
Details are provided below 
1. Open Positions: Study Director
2. Department: Toxicology-GLP
3. Qualification: PhD/M.VSC / M.Pharm / MSc in Toxicology, Pharmacology, Life Sciences
Strong knowledge of GLP regulations (OECD, US FDA, EMA)
4. Experience: 4-10 Years of industry experience
5. Work Location: Pune
6. Skill Required:
-Serve as single point of control for assigned GLP toxicology studies
-Design, execute, and oversee repeat-dose, acute, sub-chronic, chronic toxicity studies
-Ensure full compliance with OECD GLP, FDA, and regulatory guidelines
-Prepare and review study protocols, amendments, and final reports
-Monitor study progress, data integrity, and adherence to timelines
-Collaborate with QA, pathology, bioanalytical, and regulatory teams
-Handle sponsor communication and audits/inspections
7. How to Apply: 
Apply through following mail id 
Mail ID: ravi.bulla@aragen.com

Note : 
Candidates from CROS only should apply

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