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Mediception Science Pvt Ltd Requires Senior Medical Writer As a Immediate Joiner ( 02 Positions)

Mediception  Science Pvt. Ltd Requires Senior Medical Writer (On Site)  as a Immediate Joiner  Details are provided below  1. Position- Senior Medical Writer ( 02 Positions)  2..Company- Mediception  3..Job Type- On Site  4. Qualification Required- Master’s Degree or Higher in a scientific or Medical Field  5. Experience- 2 to 3 Years of Medical Content Writing.   ( Industry Medical Writing Exposure is a Must)  6. Job Responsibilities-  a. Literature Search and Systematic Literature Search.  b.  Scientific Content Writing, Medical communications  c. Slide decks and Medical marketing collaterals  d. Ability to analyse and interpret complex scientific/patient data.  e. Excellent written and verbal communication skills  f. Ability to work effectively independently and in cross functional teams  7. How To Apply- Kindly send your CV to bhawana@mediception.com  CLICK HERE FOR DETAIL...
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Required Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing)

Aurigene Oncology Requires Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing) 

Details are provided below 
1. Post -  Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing) 
2. Qualification- M. Sc. ( Specialization in any Life Sciences) 
3. Experience-  2 to 13 Years 
4. Mandatory Skills- Candidate should be from vaccine or biosimilar background, experience in Upstream Manufacturing, handling Mammalian Cell Culture, QMS. 
5. Roles and Responsibilities 
a. Responsible for optimization of CAR cells Manufacturing processes using normal human or patient derived primary blood components following ethical practices and QMS as per GMP guidelines.  
b. Actively engage in the manufacture of CAR - T cell Therapy products by diligently prioritizing the lab functions to meet critical deadlines 
c. Establish and carefully execute transductions by viral vector and non viral vector based approaches, activation and expansion of immune cells ( T cells , NK cells etc ) isolated from Clinical specimens without compromising sterility and Quality parameters as per the guidelines and defined criteria by maintaining highest standards and assist in technical transfer and core R and D activities.  
d.  To review and document SOPs , Protocols and reports pertaining to the program requirements.  
e. Work with vendors to evaluate raw materials and consumables for compatibility with the manufacturing processes. 
f. Prepare for and participate  in the compliance monitoring inspections/regulatory agency interactions. 
6. How to Apply- Interested Candidates may share their resume to gayathiri_n@aurigene.com 

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