The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and or site specific documents or essential regulatory documents and any updated or amended regulatory documentation.

Project Managers provide business and technical leadership for one or more projects within a business unit, leading project teams through the identification, justification, prioritization, initiation, development and implementation processes. This Sr. Specialist position will act as a Project Manager leading commercial launches in US and Global markets within the Pharmaceutical Business segment.

First class Post Graduate degree including the integrated PG degrees such as MS Pharm, M.Pharm, M.Tech Pharm or with specialisation in Pharmaceutics, Pharmaceutical Technology Formulation Drug delivery or equivalent. 

Evaluation and submission of application on online portal for getting domestic manufacturing and marketing permission from DCGI. Evaluation and submission of applications on online portal for import registration, import license of drugs and medical devices in India. 

As an Associate Global Scientific Advisor, you will Provide timely, accurate and credible scientific and medical input for a variety of projects pertaining to scientific communication around Novo Nordisk’s products. Collaborate closely and communicate effectively with various cross-functional stakeholders including colleagues from the US affiliate, global medical affairs, and other functional areas. Engage in dialogue with Key Opinion Leaders (KOLs) in different settings with focus on medical and scientific information. Prepare presentations for Novo Nordisk standalone events and international medical congresses.

Ph.D degree in relevant field and first class or equivalent at either Bachelors or Masters level in the relevant branch. AND Minimum of 10 years of experience in teaching, research, industry out of which at least 3 years shall be at a post equivalent to that of an Associate Professor.

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.

Analytical method development, stability samples analysis and impurities identification by using instruments like HPLC, GC, LC-MS, and other analytical techniques.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

Candidate acquainted of Quality Management System Document like Change control, Deviation and their Investigations, CAPA and Audit Management. This role will focus on ensuring the highest standards of quality throughout the manufacturing process, specifically for active pharmaceutical ingredients

Compile appendices to clinical study reports in compliance with appropriate regulatory requirements, with support of the project lead and lead medical writer. Work with internal or external Clinical and or Project Leadership functions to ensure that appendix documentation is complete and complies with the relevant guidelines.

You will be responsible for executing or assigning in-process activities during shifts, conducting line clearances, material verification, overseeing start-up of machines, and coordinating sampling activities to ensure product quality and compliance.

Support the Quality vision and mission for Amgen India aligned with Amgen’s mission to serve patients. Support Amgen India Quality Team Lead in the development and implementation of a multi-year Quality technological plan aligned with Amgens standards and overall strategic imperatives.

Bachelors degree in Pharmacy, Bachelors of Ayurvedic medicine and surgery along with Post Graduate Diploma, Degree in Hospital Administration Management from recognised University.

PhD, MD, MS, MDS in Biochemistry, Biotechnology or an equivalent degree. OR Having 3 years of research, teaching, and design and development experience after MVSc, M.Pharm, ME, M.Tech with atleast one research paper in Science Citation Indexed Journal. 

Development of a nanostructured graphene oxide, polydopamine coated PDMS nano-biosensor monitoring GPC1 for the early diagnosis of pancreatic cancer.

B.Pharma, Diploma in pharma minimum 3 year experience. ECHS invites applications to engage following Medical, Para Medical and Non Medical Staff on contractual basis in ECHS Polyclinic Akola.

Identification of key regulators and their controlling Mechanism in a combinatorial amyotrophic lateral sclerosis Network : an integrated bioinformatics analysis. Experience in computational tools, Network Biology, Molecular modeling and Simulation, Knowledge of computer programming languages with good command in oral and written communication skills in English will be given preference.