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

Required Research Fellow/Research Scientist/Sr. Research Scientist for Vaccines R and D Department and Executive/ Sr. Executive for Veterinary Vaccines Manufacturing-M.Sc./BE/M.TechBiotechnology/Microbiology/Biochemistry/Biochemical Engineering/Bioprocess Engineering

Reliance Life Sciences is Hiring for various positions for different departments at Mumbai, Navi Mumbai. Reliance Life Sciences is a medical biotechnology-led company engaged in research and development, manufacturing and marketing of differentiated medical products and services, used to treat patients primarily in intensive and critical care units in hospitals. Three core businesses of RLS are plasma proteins, biosimilars, and later generation oncology pharmaceuticals. In addition, it has initiatives in clinical research, molecular medicine, regenerative medicine, vaccines, mRNA, gene therapy, peptides and oligonucleotides. Details of the available positions is provided below  1. Department and Location Vaccines R&D - Worli & Navi Mumbai 2. Job Profile: Research Fellow/Research Scientist/Sr. Research Scientist 3. Qualification: M.Sc./BE/M.Tech Biotechnology/Microbiology/Biochemistry/Biochemical Engineering/Bioprocess Engineering 4. Experience: With 2-10 years o...
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Required Medical Writer

 Exciting Opportunity for Medical Writers
Are you passionate about clinical research and regulatory writing?
Meril Life is looking for a skilled Medical Writer to develop Clinical Evaluation Reports (CERs) for pre- and post-market medical devices. This role involves organizing and evaluating vast amounts of scientific, clinical, and medical data, ensuring compliance with MedDev 2.7/1 Rev 4, and delivering high-quality reports that drive innovation in healthcare.
1. Post - Medical Writer 
2. Job Responsibilities- 
a. Write coherent and compelling CERS based on expert analysis
b. Manage and interpret clinical trial data, literature, and real-world evidence.
c. Ensure regulatory compliance and maintain high-quality standards
d. Collaborate with regulatory, quality, and engineering teams
e. Effectively communicate scientific content in a clear, concise manner
3. What company is Looking For:
4. Educational Qualification- Bachelor's, Master's, or PhD in a scientific discipline
5. Experience-
a. 3 + years of experience in CER writing, with solid knowledge of MedDev 2.7/1 Rev 4
b. Strong background in clinical, regulatory, quality, or engineering
c. Excellent writing, analytical, and project management skills
d. Ability to work independently and efficiently
6. Why Join ?
a. Diverse and inclusive work environment
b. Opportunities for growth and knowledge transfer
c. Work on cutting-edge medical technologies
d. Collaborate with leading experts in the field
7. Send Your Resume to 
siddhiram.pareek@merillife.com

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