• 728
  • Active Jobs Found
    (Last Updated: Mar 28, 2024)
clear

Pharmacy Assistant

Advanced Superspeciality Hospitals

Full time
  • 1+ years
  • Not Disclosed
  • Gandhinagar, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 1+ years
  • Not Disclosed
  • Gandhinagar, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Qualification & Experience Any Graduate 1+ Years of Hospital Relevant Experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

  • pharma
  • Quality control
  • Inspection

Quality Control Analyst

Dr. Reddys Laboratories Limited

Full time
  • 5+ years
  • Not Disclosed
  • Vishakhapatnam, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 5+ years
  • Not Disclosed
  • Vishakhapatnam, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities You will be responsible for adhering to GLP (Good Laboratory Practices) and safety practices, and ensuring compliance with the SOP (Standard Operating Procedure). Your responsibilities include analysis of samples as assigned by the group leader, ensuring adherence to relevant SOPs and Standard Testing Protocols (STPs), and following online documentation and calculation practices. You will also be responsible for authorized transactions in SAP and LIMS (Laboratory Information Management System), as well as the online reporting of any Out-of-Specification (OOS), Out-of-Trend (OOT), and incidents to the group leader. You will be responsible for verifying that analytical results are conforming with specification limits. You will maintain and monitor 5S practices in the laboratory, perform sample management for the team and handle any other responsibilities assigned by the team leader.     Qualification & Experience 5 to 8 years of experience in a laboratory setting, preferably in pharmaceutical or related industries  

  • pharma
  • Inspection
  • Management

Medical Advisor

Dr. Reddys Laboratories Limited

Full time
  • 2+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 2+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific foundation of Therapeutic Area (TA) medical strategy. Conceptualization and project management of wide range of medical activities (including research, publications, medical education, patient support programs, advisory board meetings etc.) that are aligned to the TA Medical strategy. Engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan. Responsible to ensure optimal execution of strategic medical affairs plan through Regional Medical Affairs including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects. A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart Responsible for devising optimal training plan to ensure flow of latest medical developments in the given to sales & marketing team Jointly responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals Representing the organization in various internal & external scientific platforms Responsible for development of Medical Affairs strategic plan for identified TAs and products Ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest Responsible for identifying knowledge gaps, practice gaps and data gaps and develop strategic medical actions plans including but not limited to medical education, product education, evidence generation and special projects Collaborating with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute Receiving and processing scientific information requests received from physicians Ability to handle complex questions from health care professionals related to GGI products or disease area to satisfaction Ensure that all activities in the TA are conducted in alignment to Dr. Reddy’s COBE (Code of Business Ethics) Policy and compliance guidelines Responsible for ensuring that all promotional, physician and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy’s Promotional Material approval policy Product pipeline champion with an ability to identify unmet needs through active stakeholder interactions and actively contribute in the new product ideation and development of differentiated products   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

  • Inspection
  • Management
  • Communication

Medical Advisor - Oncology

Dr. Reddys Laboratories Limited

Full time
  • 3+ years
  • Not Disclosed
  • Delhi, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 3+ years
  • Not Disclosed
  • Delhi, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities This role is HO based vacancy where travelling will be around 06-07 days in month. Candidate who are having Oncology & Hematology experience are only preferred. Entire Relocation cost will be borne by the company & initial 15 days stay will be provided in case of relocation to one city to another.     Qualification & Experience MBBS + MD Pharmacology doctors. Candidates who are currently working as Regional Medical advisor / Area Medical advisor with 3+ years of experience in oncology segment can apply for this role.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

  • mbbs
  • MD
  • Operations
  • Inspection

US Medical Omnichannel Lead-Associate Director

Eli Lilly and Company

Full time
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 10+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Direct the delivery team to take ownership and deliver best possible outcomes through a sound data management, analytics and operations mindset. Work closely with stakeholders to ensure expansion and penetration of Omni use-cases with medical teams. Create a framework for communication, project management and execution across BUs to help drive best practices Take ownership of design, development, maintenance and operations Be a mentor for team members, and drive upskilling plans for LCCI team Serve as trusted career advisor, and work with functional leadership and HR to identify career opportunities for these team members, both systemically (career path development) and with individuals as needed Develop a pipeline of right talent and leadership, and contribute to an inclusive community of analytics expert practitioners Drive standardization, automation agenda across business units to help scale the delivery operations     Qualification & Experience Master’s degree in management/ pharmaceutical or a related field from a premium college Bachelor’s Degree with 12+ years of relevant experience in an allied fucntions such as: BI, data analytics, Omnichannel, integrated marketing, supporting Pharma/Lifesciences Commercial or Medical ops internally or in consulting; at least 6+ in leading teams  

  • pharma
  • Quality control
  • Management

Associate Medical Advisor

Eli Lilly and Company

Full time
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Product or Molecule Safety Physician / Lead Physician Provide global medical leadership and input into all aspects of safety of assigned product(s) including surveillance programs and risk management planning. Ensure proactive safety surveillance: lead risk management activities for assigned products globally lead and guide the surveillance activities of scientists on the team including signal detection and clarification activities and risk evaluation activities; provide support, training and continued improvement as appropriate manage decisions and actions to be taken, including communication to appropriate customers (e.g., Product Teams, Management, Affiliates and Regulators) and liaise with GPS Medical Area Directors and with Lilly Medical Therapeutic Area Team Leaders and Directors, as appropriate, to fulfill safety obligations; Supervise and review reports on safety issues and their implications for the Core Safety Information and Core Risk Minimization Activities, represent PV position to Global Patient Labeling Committee and/or the Safety Review Committee as appropriate. Build collaborative working relationships with other Global Patient Safety Physicians and development and brand teams medical globally to ensure full cooperation and high quality medical evaluation of safety data for global regulatory purposes. Represent GPS Medical and/or Product on appropriate committees/product development and brand teams. Provide medical support for Global Patient Safety activities and reports within the department, as appropriate. Provide Global Patient Safety expertise to internal customers (e.g., regulatory, early phase development, business units). Provide medical input for review of Adverse Event cases. Lead process and provide medical input for review of Suspected Adverse Reactions Demonstrate knowledge in pharmacovigilance and risk minimization, which includes understanding of relevant aspects of laws, regulations and guidance. Understanding and Support of the QPPV role Understanding the roles and responsibilities of the European Union Qualified Person (QPPV) and ensure their involvement in the pharmacovigilance system and processes. Ensure support and information are provided to enable the QPPV to fulfill all the QPPV legal responsibilities. Training, coaching and mentoring Provide training, coaching and mentorship to safety surveillance scientists, and other GPS Medical physicians and clinical research scientists with respect to medical aspects of safety surveillance Provide Global Patient Safety training for development and brand team physicians and clinical research scientists and other audiences (e.g. Regulatory, Lilly Medical) as appropriate. Maintain compliance with Lilly Red Book and corporate policies, Lilly Research Laboratories and Global Patient Safety curriculum map. Maintaining compliance with the Lilly Corporate Integrity Agreement. Global Patient Safety Leadership  

  • pharma
  • Management
  • Communication

Medical Affairs – Medical Writing

Eli Lilly and Company

Full time
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 2+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data. Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version. Ensure and coordinate quality checks for accuracy. Exhibit flexibility in moving across development and preparation of multiple document types. Influence or negotiate change of timelines and content with other team members. Work with internal and external experts to develop and prepare presentations. As needed, may build and manage relationships with vendors/alliance partners.     Qualification & Experience Graduate degree with formal research component or in life sciences. Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields. Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise). Experience writing regulatory, clinical trial documents and/or publications  

  • pharma
  • Medical Writing
  • Clinical Trial

Senior Scientific Writer

Sanofi Aventis

Full time
  • 4+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 4+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities People: (1) Maintain effective relationships with the end stakeholders within the allocated GBU and product – with an end objective to develop education and communication content as per requirement for HEVA communications; (2) Interact effectively with healthcare professionals on publication content; and (3) Constantly assist other writers (junior) in developing knowledge and sharing learning Performance: (1) Create HEVA communications deliverables (including manuscripts, posters, abstracts, and slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams as per agreed timelines and quality; and (2) Provide strategic support with individuals and institutions, which may serve as resources for publications purpose, etc Process: (1) Develop complex publications material; (2) Act as an expert in the field of medical communication for the assigned therapeutic area; (3) Assist the assigned scientific communication team in conducting comprehensive publication-needs analysis; (4) Manage core HEVA communication processes, templates, and products across the portfolio in accordance with the scientific and value messages aligned with Core Value Dossier, the US AMCP Dossier, and HEVA contributions as appropriate to other submissions; (5) Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products; (6) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (7) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (8) Implement relevant element of publication plan and associated activities for the year identified for the region; (9) Work with selected vendors within the region to deliver the required deliverables as per defined process; and (10) Design an overall plan of action based on end-user feedback and improve course content and delivery Stakeholder: (1) Work closely with HEVA global and local teams, RWE global and local teams and scientific communication teams in regions/areas to identify publications needs and assist in developing assigned deliverables; and (2) Liaise with HEVA global and local teams to prepare relevant and customized deliverables     Qualification & Experience Experience: >4 years of experience in content creation for the pharmaceutical/healthcare industry, or academia Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills: Relevant training/experience in health economics, public health, epidemiology, or other relevant health-related scientific discipline (including but not limited to therapeutic area/domain knowledge exposure; knowledge of Good Publication Practice; publication submission; and/or project management) Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree  

  • pharma
  • Medical Writing
  • Communication

Expert Medical Information writer

Sanofi Aventis

Full time
  • 8+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 8+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise. Performance: 1) Provide SME support and high-quality completion of deliverables (local and custom scientific response documents, US FDA Annual Reports, and Compendia Reviews) as per agreed timelines and quality. 2) Supports delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards with the agility to learn and contribute to situations of demands. 3) Ability to multi task and manage different type of projects simultaneously. Process: 1) Act as an expert in the field of medical information writing with project management skills and maintain the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process. 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery. 6) Capable of identifying risks to processes and proposing mitigation plans through the application of a problem-solving mindset. Stakeholders: 1) Work closely with medical teams in countries/regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables. 3) Collaborate with the Global Medical Information team and country medical information teams as relevant.     Qualification & Experience Education: Advanced degree in life sciences/pharmacy/similar discipline (Ph.D., Master, or bachelor’s in science, D Pharms) or medical degree (MBBS, BDS, BAMS, BHMS, MD) Experience: ≥8 years of experience in content creation in medical or scientific writing for the pharmaceuticals/healthcare industry, or equivalent experience in the clinical setting, pharmacovigilance; At least 4 years of direct medical information writing experience in the pharmaceutical company; Minimum 2 years of experience in managing global, cross-functional project teams, working in a Matrix environment, and acting as an SME, mentor or guide. Soft skills: Excellent communication skills (written, verbal, and presentation), Stakeholder management; and ability to work independently and within a team environment.  

  • pharma
  • mbbs
  • Medical Writing

Manager- Regulatory Affairs

Sanofi Aventis

Full time
  • 8+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024
  • 8+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Mar 27, 2024
  • End Date: May 27, 2024

Responsibilities Writing of renewal dossiers of products manufactured in Indian CMO’s and exported to Russia, Ukraine, other CIS countries, Sri Lanka, Nepal, Latin American countries and other countries (if any addition) etc. Writing and review of new product dossiers/ renewal dossiers for products manufactured at CMO’s based in South Korea, Thailand and Philippines for export markets. Maintenance of the entire renewal dossier and new product dossiers for Indian CMO’s and overseas CMO’s. Preparation and submission of post approval variations and send proper communication for implementation of the change. Co-ordination with GRA, Country regulatory affiliates and COE for submission of dossier and supporting the required documentations. Consolidate the regulatory strategy with the affiliate or the Global RA to submit the site change Updation of eTOC and dispatches dossiers through Veeva Vault. Maintenance and distribution of Normative document to the responsible quality manager. Implementation and follow GRA processes for all export product dossier management. Life cycle management for all the products managed by EM India.     Qualification & Experience B.Pharm/ M.Pharm/ MSc in lifesciences Experience: (8-12 years of experience in Regulatory Affairs, Quality Assurance)  

  • bpharm
  • mpharm
  • Regulatory Affairs

×