Job Opening: Apprentice Trainee - Microbiologist (API Industry) Details are Provided below 1. Company: Asence Pharma Pvt 2. Department: Quality Control -Microbiology 3. Location: Ranoli, Vadodara 4. Role Overview: Company is looking for a dedicated and enthusiastic Apprentice Trainee - Microbiologist to join their Quality Control Microbiology team. This role offers a great opportunity to gain hands-on experience in microbial analysis, environmental monitoring, and aseptic techniques in an API manufacturing environment. 5. Eligibility: B.Sc. / M.Sc. in Microbiology or Biotechnology 6. Key Responsibilities: -Perform environmental monitoring (EM) of cleanrooms -Carry out microbiological testing of raw materials, water, and finished products -Maintain proper documentation as per GMP guidelines -Assist in validation and sterility assurance activities -Adhere to safety and quality procedures 7. How to Apply: Send your updated resume to hr@asence.com with the subj...
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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