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Multiple Vacancies - Required Freshers and Experienced including Internship Opportunity with Stipend and Food and Accomodation - Microbiology/ Biotechnology/ Chemistry/ Life Sciences

Required Freshers or Experienced including opportunity for internship at  Biofertilizers & Biopesticides Manufacturing Unit  Required qualified and motivated professionals for  expanding biofertilizers & biopesticides production facility. Details are provided below  1. Company: Pranad Bio Inn 2. Location: Pirangut, Pune, Maharashtra 3. Open Positions :  (The Paid Internship Offer - 4 months duration) 1) Microbiologist / Biotechnologist -Culture development, fermentation & strain maintenance  -Quality control (CFU count, contamination check) -Product stability & documentation Qualification: MSc Microbiology /Biotechnology Experience: 0-3 years (Freshers may apply) 2) Production Chemist /Bio-Process Executive -Batch preparation (liquid & carrier-based products) -Mixing, formulation & SOP compliance -Production documentation Qualification: BSc / MSc Chemistry /Life Sciences Experience: 1-3 years 3) QC Microbiologist / Lab Te...
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Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc.

Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc. 
Details are provided below 
1. Post - Research Associate ( Report Writers) 
2. Company- Synergen Bio Private Limited Pune 
3. Department- Project Management and Biopharmaceutics 
4. Qualification- B  Pharm,  M. Pharm, M. Sc. 
5. No. Of Vacancies 02 
6. Experience- 1.5 + Years 
7. Note - Immediate Joiners preferred 
8. Job Location- Shivajinagar , Wakdewadi , Pune 
9. Tasks Responsibilities- 
a. Preparation of Clinical Study Report ( CSR) within proposed time line according to raw data and as per the regulatory requirements.  
b. Preparation of electronic copy of final reports ( scanning , book marking , hypertext linking , inherit zoom and creating TOC to PDFs 
c. Know about eCTD specifications guidelines for regulatory submissions 
d.  Coordination with Clinical, Bioanalytical department and principal and investigators while preparation of Clinical Study Report and compilation of data .
e. Data uploading ( demographies, Clinical laboratory values , vital signs , meal distribution, and Deviation of sample time point.) 
f. Preparation of relevant report appendices as per project.  
g. Coordinating with different sections with projects related activities.  
h. Preparation of regulatory summary reports in Module 02 and clinical study reports in Module 05( i e. eCTD Format) 
10. Interested candidates share CV on careers@synergenbio.com 
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