Responsibilities Design and execute marketing initiatives for Oncology franchise to drive scientific dissemination Identify and drive critical new initiatives to drive business growth Support development of strategic road map for our Oncology franchise in India Monitor, analyze, and evaluate market trends, consumer behavior and competitor activity to identify market opportunities; adjust marketing strategy and plan to meet changing markets and competitive conditions. Plan budgets for marketing initiatives, including alignment with relevant India / Regional stakeholders Conduct ongoing business and financial review of business development opportunities Build business cases and ensure approval of identified opportunities with new product/indication launches Execute indication launch strategy Design templates to monitor launch efficiency, in alignment with compliance controls Plan and achieve monthly objectives for the upcoming indications through regular monitoring of the market trends, planning the short and long terms strategies and driving initiatives to support the plan. Monitor upcoming indication launches for competitors     Qualification & Experience Education Bachelor’s Degree or higher (Science equivalent/MBA) Experience Experience in top pharma marketing (preferably oncology) Project Management Excellent organizational and project management skills to manage and oversee the timely implementation of patient program activities in line with compliance controls  

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 regulatory content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical regulatory writers in developing knowledge and sharing expertise Performance: 1) Provide deliverables (CSR, CO, SCE, SCS, SCP, SBP, PBRER, ACO, RMP, ID Cards, clinical evaluation report, Briefing packages, HAQs, Immunogenicity reports) as per agreed timelines and quality 2) Fair understanding of Product Alerts, and trial transparency documents with the agility to learn and contribute to situations of demands Process: 1) Acts as an expert in the field of medical regulatory writing and maintains the regulatory requirement for countries supported. 2) Assist the assigned medical team in conducting comprehensive medical regulatory writing-needs analysis. 3) Implement relevant elements of the medical regulatory plan and associated activities for the year identified for the region. 4) Work with selected vendors within the region to deliver the required deliverables per the defined process. 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery 6) Substantial understanding of Product Alert Process and Trial Transparency documents with the ability to quickly develop expertise and contribute swiftly if the situation demands Stakeholders: 1) Work closely with medical teams in 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 CTT, CST, GCT and SMT. 4) Proactively liaise with the Clinical/Medical/Pharmacovigilance/Biostats/Regulatory/Legal/Regulatory/Corporate Affairs departments to prepare relevant & customized deliverables.     Qualification & Experience Experience: ≥8 years of experience in regulatory writing for the pharmaceuticals/healthcare industry Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment, leading project teams Technical skills: As applicable (including but not limited to therapeutic area/domain knowledge exposure; publication submission; and/or project management; Expert knowledge of and demonstrated accomplishment in global registration of drugs) Education: Advanced degree in life sciences/ pharmacy/ similar discipline (PhD, Masters, or bachelor’s in science, D Pharma, Pharm D) or medical degree (MBBS, BDS, BAMS, BHMS, MD)  

Responsibilities Supporting the Quality Assurance manager to ensure timely handling of product complaints. Take care of the EM CHC Europe complaint management inbox Ensure overview of incoming complaints and monitoring of due date at the CMO and EM CHC Europe site Assignment of incoming Complaints to the respective CMO Assessment ad categorization of the complaint Recurrence monitoring Corrective & preventive actions follow up Documentation of investigation in the system Closure of the complaint in the system Potential exchange with the affiliate Contribute to the monitoring / trending of complaints. Monthly KPI evaluation and reporting Preparation of summary for Product Quality Reviews Contribute in the annual CMO Risk ranking exercise     Qualification & Experienc 3 years in pharmaceutical environment, preferably in Quality, i.e. quality control/assurance, systems quality assurance and/or quality systems management experience in external quality management activities Qualification in Pharmacy or Natural Sciences  

Responsibilities Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement; (2) Actively lead and develop SBO operation activities; and (3) Ensure new technologies are leveraged Performance: (1) Ensure publication/medical education materials (slide decks, abstracts, posters, and manuscripts etc.) are delivered, stored as per agreed timelines and quality; (2) Develop tools, technology, and process to constantly improve quality and productivity Process: (1) Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports; (2) Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the medical writing group; and (3) Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards Stakeholder: (1) Work closely with scientific communication/medical content enhancement teams to ensure the end-to-end effective project delivery of the designated publication/medical education deliverables     Qualification & Experience Experience: 3-5 years post qualification experience Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment. Technical skills: Project management; Scientific/Medical writing/communications; Pharma experience (including but not limited to therapeutic area/domain knowledge exposure; and/or publication submission). Hands on experience with MLR process and exposure to relevant tools such as Veeva PromoMats or similar is desirable. Education: University degree level (Graduate degree, preferably in science). Additionally, relevant advanced/postgraduate degree in life sciences/pharmacy/similar discipline desirable  

About The Internship They are looking for a Content Development Intern to create and design content for pharmaceutical and medical professionals.   Eligibility Lifesciences and pharma graduates can apply. Basic understanding of pharma and healthcare industries. Clear and concise writing style, attention to detail and language abilities. Basic knowledge of Google Workspace and Canva.   Duration Please note that this is an unpaid 2-month internship with the potential for paid continuation and full-time employment opportunities for exceptional candidates!   Note: Only Motivated pharma students who are in the first and second year of their graduation/ first year of post-graduation, please apply.  

Responsibilities Performs in vitro cell based assays and binding assays using Biacore. Performs PCR, RT-PCR, qPCR, ddPCR and gel electrophoresis etc. for mAbs, vaccine and CGT products· Develops and evaluates methods used for the measurement of biological attributes, develops  validation protocols, and execute the validation plans. Prepares final report and presents data as applicable Evaluates and analyzes scientific reports and identifies next steps and key challenges. Plan and conduct research projects independently Works with cross-functional teams within the organization to solve/support both technical and process-related issues. Performs peer-review of data along with collaborative test and research reports Keeps abreast of current trends and developments in related scientific fields, particularly in functionalm assays, binding assays, impurity analysis in mAbs, CGT and vaccines. Demonstrates strong technical skill, interest, and expertise in binding, functional and viral assays Actively engages in overall project and ensures own work is aligned with overarching goals Shares technical expertise with junior fellow lab staff and serve as a mentor for them Seeks out innovative ways to apply knowledge or skills to improve protocols and results Assists team lead in planning, implementing, and evaluating laboratory procedures/systems Supports in departmental trainings as applicable. Attends scientific seminars and conferences Follows GLP and QMS practices. Recommend improvement to systems and all other supporting activities as assigned by the team lead. Participates in internal and external audits. Aligns with USP's mission, and complies with USP's guidelines and other requirements Performs other duties as assigned.     Qualification & Experience   The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience M.Sc. in Biochemistry, or related Biological Science field with 6-8 years of Industrial experience in Bio pharmaceutical product development and quality testing, potency assay, mAb functional and binding assays (using Biacore) and molecular biology techniques. Able to analyze and interpret data using appropriate statistical software/methods and calculation for relative potency determination. An equivalent combination of education and experience may be substituted. Laboratory experience must include expertise developing and validating assays, technology transfer for monoclonal antibodies and vaccine testing, ELISA, advanced PCR techniques, viral assays.  

Responsibilities Executing the analytical tests allotted by Project Leader or Group Leader. Responsible for completing the project as per the timelines and troubleshoot the scientific aspects of the projects on need basis. Coordination with group leader to ensure completion of the projects allotted to the team. Responsible for sample archival, sample tracking and chemical inventory tracking in the laboratory. Responsible for the initial review of the project reports, documents and assisting the group leader when required. Taking up any additional responsibilities assigned by group leader from time to time. Responsible for preparation and review of SOPs, protocols, reports etc. Responsible for performing the calibration of the equipment as per the schedule. Responsible for preparing, executing, and completing IQ/OQ/PQ of new instruments. Ensuring that the chemicals and column etc. are available for the projects and forward the purchase requisitions. Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification. Responsible to maintain and follow QMS and should handle incidents and deviations. Supporting Verification, GPH, PQM, stability and other departmental teams in terms of testing and project review whenever needed.   Qualification & Experience Must have a Master’s degree in M.Sc. (analytical or organic), M. Pharma (pharmaceutical sciences or analysis) with 3 to 6 years relevant laboratory experience. Proven track record of consistently in completing the tests on time, with high quality for formulation and API’s. Proficient in chromatographic analysis, particularly in HPLC, GC. Proficient in handling other related analytical instruments such as Auto titrator, KF, FTIR, UV spectrometer, Thermal equipment’s, Elemental analyzer, SOR, TLC etc. Proficient in wet chemical analysis.    

Responsibilities Support the development, implementation and monitoring of Quality programs, policies, and procedures to ensure compliance with certifications/accreditations requirements, corporate policies, and procedures. Review/approve the following: Quality-related issues, complaints, deviations, and investigations with appropriate corrective/preventive actions. Review/approval of technical and analytical documents of moderate to high complexity for reference standard development Review/approval of change controls Method validation reports Equipment IQ/OQ/PQ documents Batch Records Lab data projects Track and trend different elements of the quality system and report on the progress of the programs, including areas of strength and opportunities for improvement on a regular basis. Drive continuous improvement initiatives across the organization utilizing quality methodologies to optimize processes and enhance efficiencies. Lead internal process/target audits according to a pre-defined schedule. Support the Supplier Quality Management program by conducting supplier evaluations, audits, and supplier performance/metrics. ISO 9001/17025: Participates in ISO 9001, ISO 17025, and other certification/accreditation activities. Performs other duties as required.     Qualification & Experience Master’s degree in science area (Chemistry, Biology) and a combination of skills and experience in the pharmaceutical or related industry. A minimum of 8-12 years of experience in Quality, including developing and implementing a Quality Management System

Responsibilities Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: Ensure Quality Operations / Quality Assurance in compliance with applicable regulations and policies, including FDA, Safety and Environment. Improve overall efficiency of the Quality Assurance/Quality Operations through use of Process Excellence, Lean principles and Data analysis. Communicate, align, drive & periodically review departmental objectives and metrics with the team members. Assure personnel are properly trained and developed for their function and future responsibilities. End to End Governance of In-Process Quality Assurance process. Drive QA Controlled document issuance process. Support Finished Goods release process. Conduct Batch release in SAP system. Ensure resolution of daily quality operations FG release related issues. Perform Review and Approval of Batch Manufacturing Records (FG & Non-Abs) and FG testing records and take disposition decision of Finished Goods after review of BMR and Test reports.   Qualification & Experience A graduate in Pharmaceutical Sciences / Postgraduate in Science with minimum 4-6 years relevant experience in Quality Assurance / Quality Operations function. Experience working in both an FDA and European regulatory environment is preferred. Green belt certification in lean six sigma with demonstrated experience in quality projects. Experience of working in a regulated industry like Pharmaceutical / Medical Devices is highly desirable. Working knowledge of Software's for Complaint management, Change control process, NC/CAPA applications etc. is preferred.  

Qualification & Experience MBBS with TSMC Registration 5-7 years of experience in Clinical Administration in any reputed Hospital     Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"