Carrying out research and experiments related to the project. For example, fabrication, characterization, and performance optimization of sensors. Analyzing and interpreting data, documenting research findings.
Masters degree with specialization in Clinical Research, Clinical Trials or Clinical Data Management, Pharmacovigilance; Technology development and clinical validation of an injectable hydrogel for repair of Articular Cartilage Defects
First class Post Graduate Degree, including the integrated PG degrees. Research experience in Pharmaceutics, in vitro cell culture, molecular-based techniques, and animal handling. Investigating the therapeutic potential of refractory status epilepsy
M.Pharm in relevant discipline from reputed institution. First Class at Bachelor with Master Degree in the appropriate branch of specialization in Pharmacy from an institute approved by Pharmacy Council of India.
Post-graduate degree in Life Science from a recognized university. Proven and excellent written and verbal communication skills in English, with proven ability to write different types of content for a diverse audience.
Bachelors in Pharmacy or Masters in Chemistry, Sciences, Biotechnology ,Biomedical Engineering; Provide regulatory metrics on performance that are aligned with Area & GEM Regulatory Affairs criteria to measure regulatory performance to LOC, Area & Regional management
Collaboration with internal and external media to ensure the proper execution of strategies. Providing training, product knowledge, and direction to the field sales team to ensure that they are well-equipped with scientific and communication skills both.
First class M.Sc in Biological Sciences, Biotechnology, Pharmaceutical Sciences, Chemistry. Applicant must be qualified in any one of the following tests CSIR, UGC, ICMR including Lectureship
Ph.D. degree in any branch, specialization in Pharmaceutical Sciences from University of repute. Masters degree in appropriate branch of specialization in Pharmacy with Bachelors degree in Pharmacy with minimum 60% marks or equivalent.
Monitor the API, formulated products against stipulated conditions mentioned in the batch production record. Conduct certification of batch production records for compliance and stage wise completion.
Bachelors degree in a scientific, health, communications, technology health related field. Demonstrated experience in technical/ regulatory scientific writing.
The Center for Nanomedicine (CNM) is a unique translational nanotechnology research institute located at the Johns Hopkins School of Medicine. It brings together engineers, basic scientists, clinical researchers and clinicians working under one roof on translation of novel delivery technologies for therapeutic applications and has a strong record of clinical translation.
Masters, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent
MSc. in Life Sciences. Prior experience in molecular biology techniques, expression and purification of proteins, mammalian cell culture, and cellular signaling assays are desirable but not essential.
Masters, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University
Doctoral Degree in Science from a recognised university or equivalent in Biochemistry, Biotechnology, Stem Cell Biology and Neurobiology, Neuroscienc e with a strong publication record and research experience in Cell Biology, Molecular Biology and Neurobiology.
Women researchers who have completed M.Tech. in Biotechnology or in allied areas, M.Pharma, equivalent Degree holders. Candidates who are registered or enrolled in higher studies, Ph.D and or receiving any fellowships are not eligible to apply.
Preparation of original DMF, amendments, Annual reports and Review of adequacy of documents for submission. Compilation, review and submission of various Drug master files for US, EU, TGA, Canada and other markets as per respective regulatory guidelines and checklist
B.Pharm, M.Pharm, B.E, B. Tech with 6 to 10 years of experience in Supervising and Controlling Production areas like Aseptic Filling, Vial Washing, Autoclave, Lyophilizer, Visual Inspection and Packing. Should have knowledge of QMS activities