December 2024

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.

Masters, Integrated Masters Degree in Natural or Agricultural or Pharmaceutical Sciences from a recognized University OR Bachelors degree in Engineering or Technology or Medicine from a recognized University

B. Pharmacy from a recognized Institute Or Approved Diploma in Pharmacy from an Institute recognized by the Pharmacy Council of India and registered as Pharmacist under the Pharmacy Act.

A randomized, double-blind, parallel group, placebo-controlled multicenter study to evaluate efficacy, safety and tolerability of ianalumab in participants with diffuse cutaneous systemic sclerosis

Knowledge of Documentation, QMS, Deviation, Change Control, Market Complaint, OOS, OOT, Validation Qualification, IPQA, Audit Compliance.

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients. Formulation development of Pharmaceutical & Medicinal Devices. Execution of successful technology transfer at commercial site.

This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent will support the reference standard program within the Global Biologics department. The incumbent in this role will focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards.

Well-versed with QC related activities of Pharmaceutical Manufacturing Industry. Knowledge of CGMP & Safety Guidelines.