The candidate needs to be involved with trial registration, participant screening, recruitment, obtaining informed consents, maintaining longitudinal follow-ups using REDCap forms, ensuring GCP compliance, conducting periodic review meetings with site PIs and trial coordinators, troubleshooting issues, review data and generate reports periodically and draft manuscripts, publication materials, engage with stakeholders for recruitment campaigns and manage funding body requirements.

B.Pharmacy or 10 plus 2 with Science stream PCB and Approved Diploma in Pharmacy. Min 03 years exp.

B.S. 4 years programme, B.Pharm, MBBS, Integrated BS-MS, M.Sc, BE, B.Tech or equivalent degree, with 55% marks and passing of NET, GATE test. Project FISHING OUT MECHANORESPONSIVE HYDROGELS THROUGH CHIRAL ORCHESTRATION IN AMOHIPHILIC PEPTIDES : A POTENTIAL THERAPEUTIC TO CANCER AND MICROBIAL CHALLENGES

Conduct QC testing on raw materials, packaging, stability, in-process, and finished products. Capable of Handling Instrument like HPLC, GC,KF, IR,UV instrument. To review analytical data & handling of QMS i.e. Deviations, 00S, 00T, Laboratory incidences, OOC, CAPA and Effectiveness of CAPA.

Monitor and supervise production process to ensure compliance with SOP and cGMP. Maintain documentation as per regulatory authorities requirement like change control, deviations. Highlight technical problems and take corrective actions.

Ability to build clinical or regulatory arguments in the absence of direct data using logic, analogy and therapeutic area science. Understanding of medical practices regarding procedures, medications, and treatment for different disease states.

areas of life science/ medical device/pharmaceuticals/ engineering / science; Experience in the area of orthopedic, neurological, ocular implants or Biosensors or IVDs or therapeutic devices Drug-device combinations with proven track record through published high-impact research papers, patents and product development.

D.Pharma, B.Pharma. Must be registered in A.P. Pharmacy council with up to date renewal. Age No person shall be eligible for appointment if he, she is less than 18 years of Age and if He, she is more than 42 years of age as on 1.7.2024.

Zoledronic Acid in Preventing Worsening of Bone Health in Postmenopausal Women with Nonmetastatic Carcinoma Breast Receiving Chemotherapy, A multicenter Randomized, Double- Blind, Placebo-Controlled Study. Proven experience in coordinating and managing RCTs or interventional studies with published research papers.

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 1948.

Designing, development and evaluation of anti-thrombogenic factors loaded small diameter vascular graft with superior mechanical and biological properties for cardiovascular tissue reconstruction application. M.Sc, M.Tech, First class Engineering Graduate degree of 4 years in any field of Life Sciences, Biotechnology, Biomedical Engineering.

direct recruitment of Faculty on a regular basis through open competition; Ph. D. with first class or equivalent grade at the preceding degree in the appropriate branch, a very good academic record throughout, and Teaching/ Research/ Industrial experience with published work of high quality. Well- recognized and established reputation for having made a conspicuous seminal contribution to knowledge in pharmaceutical and allied areas. 

PhD or MBA, PGDM or PMP certification with any science, engineering, management bachelor degree with 3 years of experience in startup incubators or MSc, MTech, MS, M.Pharm, ME with at least 5 years of experience in startup incubators. 

Identification of plasma micro RNAs biomarker in severe Traumatic Brain Injury Patients, a case-control study. Master in Life Sciences, Biotechnology, Biochemistry, Microbiology, forensic science and allied subject obtained from a recognized University, Institute.

FP / Stability / Analytical Instrumentation-HPLC, UV and Dissolution. Handling of LIMS, Empower software, HPLC Waters and SAP. Granulation Integrated line, Make-GEA / Glatt; Compression KORSCH, SEJONG, GEA, CADMACH; Capsule Filling; Liquid Manufacturing area

Post Graduate Degree in Molecular Biology, Biotechnology, Life Sciences, Basic Science OR Graduate, Post Graduate Degree in Professional Course, selected through National Eligibility Tests - CSIR, UGC NET including lectureship Assistant Professorship or GATE.

M.Pharmacy Pharmaceutical Analysis / M.Sc. Analytical chemistry; Good knowledge of the Academic subjects. Know the R&D instruments like Rapid mixer granulator Compression machine, Coating machine. Roller compactor, Manual Capsule Filling Machine & Blender Machine.

interface with the Amgen Global, Site, Biosimilars, and/or Device RA CMC teams for specific strategies or activities that impact a product. Lead submission for annual reports, facility registrations, facility renewals, and product renewals. Interact with authors, reviewers and subject matter experts with respect to delivery of CMC documents required for regulatory submissions.