1.0 - 5.0 years

0 Lacs

maharashtra

On-site

The main purpose of your role as an experienced professional individual contributor in Medical Affairs is to work under limited supervision and apply your subject matter knowledge effectively. Your capacity to apply skills and knowledge should meet specific needs or requirements within the field. As an experienced professional in the Medical Affairs Sub-Function, you will be responsible for overseeing the direction, planning, and execution of clinical trials and research activities. You will play a key role in data collection, implementation of clinical protocols, and ensuring completion of final reports. Additionally, you will be involved in recruiting clinical investigators, negotiating study designs and costs, and directing human clinical trials, specifically phases III & IV for company products under development. Your responsibilities will also include participating in adverse event reporting, safety responsibilities monitoring, coordinating reporting information for submissions to regulatory agencies, monitoring adherence to protocols, and determining study completion. Furthermore, you will coordinate and oversee investigator initiations and group studies. You may also act as a consultant or liaison with other corporations when working under licensing agreements. In terms of education, you are required to have an Associates Degree (13 years), and a minimum of 1 year of relevant experience in the field. Your role demands a high level of professionalism, attention to detail, and the ability to work effectively within a team environment to achieve the goals of the Medical Affairs Sub-Function.,

Posted 5 days ago

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Certification Specialist Classic Search Private Limited

8.0 - 12.0 years

0 Lacs

karnataka

On-site

You should have 8-10 years of experience and a B.Sc./M.Sc. (Agri) or equivalent education with proven experience in certifications. Experience working in a commercial organization of scale and in the field of organic certifications with different agencies is required. Your key responsibilities will include spearheading and delivering end-to-end organic certification requirements of the company, collaborating closely with agriculture, processing, and finished goods teams. You will interact with regulatory agencies, respond to inquiries and submissions, and represent the company during inspections and audits. Experience in implementing Quality Management System (QMS), Vendor due diligence, strengthening contract manufacturing units, and ensuring robust compliance measures is essential. You will lead the process for obtaining and renewing certifications as per NPOP, NOP, and EU standards. Additionally, you will require certifications such as FFL, Regenerative agriculture, GAP, GFCP, etc. for farming on organic lands. If you have relevant experience in obtaining certifications for farming/agriculture teams, you can email your profiles to poornima.c@classicsearchplc.com.,

Posted 5 days ago

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