Mohali

Ph.D Chemistry, Medicinal Chemistry, Biology, Pharmacoinformatics, Bioinformatics or related area. Candidate must have at least one research paper in a science citation indexed journal. Candidates who have submitted their PhD thesis in the above subjects will also be eligible along with proof of submission to apply. 

Research Associate I under a project entitled Peptide-metal chelator conjugates as potential therapeutic candidates for multifaceted amyloid-β toxicity in Alzheimers disease sponsored by Anusandhan National Research Foundation, GoI, New Delhi

Candidate should have knowledge of FG, HPLC, AAS, Potentiometer and related instruments for stability section. Candidate should have knowledge of IPQA activities in packing and manufacturing areas. Responsible for documentation and cGMP guidelines.

Degree in Medical or Human Genetics, Life Science,Nursing, Clinical Psychology, Social Sciences, Social Work and Equivalent in Related Fields. Candidates should have minimum one year Hands on experience in Genetic counselling, preferably in cancer genetic counselling.

Research Associate III under a project entitled The Technical Resource Centre under the Centre for Evidence for Guidelines by NIPER sponsored by Department of Health Research, Ministry of Health and Family Welfare Govt. of India, New Delhi GP-482 under Dr. Dipika Bansal, Associate Professor, Department of Pharmacy Practice, NIPER-SAS Nagar.

1st class Masters Degree in Biotechnology, Chemistry, Biochemistry, Food Science from a recognized University OR 1st class B. Tech Degree in Biotechnology, Food Technology from a recognized University

Post graduate degree in any branch of life sciences, biotechnology or Graduate, Post Graduate in any branch of life sciences or biotechnology or Post Graduate in any branch of life sciences, biotechnology selected through National Eligibility Tests-CSIR UGC NET including Lectureship and GATE.

Awareness of global regulatory reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting.

To ensure that the products are manufactured and stored as per appropriate documents in order to obtain the required quality. To ensure that the production records are reviewed as per current procedures.