ResponsibilitiesLead brand and marketing strategy for Vazokare Cardio portfolio; drive growth, new launches, and lifecycle management; manage product teams, campaigns, and digital initiatives; coordinate cross-functional execution; ensure regulatory compliance; and build high-performing teams.Qualification & Experience 18+ years of pharmaceutical marketing experience in cardiology; strong commercial and analytical skills; proven leadership; Science/Pharmacy degree (MBA preferred).

ResponsibilitiesCoordinate the end-to-end process of preventive health check-up packages.Schedule appointments for individual and corporate health check clients.Register patients in the Hospital Information System (HIS).Explain available health check packages, pricing, preparation instructions, and inclusions.Coordinate with laboratory, radiology, cardiology, nursing, and consultant departments to ensure timely completion of investigations.Ensure minimum patient waiting time by monitoring service flow.Assist patients throughout the health check journey and resolve service-related queries.Coordinate with corporate clients regarding employee health check schedules.Verify patient documents and maintain accurate records.Support billing, payment collection, invoice generation, and receipt issuance.Ensure timely delivery of health check reports to patients and corporate clients.Maintain confidentiality of patient medical records.Prepare daily, weekly, and monthly MIS reports related to health check services.Follow NABH standards, hospital policies, and patient safety protocols.Coordinate with marketing and corporate relations teams for health camps and wellness programs.Collect patient feedback and support continuous service improvement.Handle patient complaints professionally and escalate concerns when required.Qualification & Experience Bachelor's Degree in Hospital Administration, Healthcare Management, Life Sciences, Commerce, Business Administration, or any related discipline.Certification in Hospital Administration is an added advantage.

ResponsibilitiesReceive, label, process, and analyze various clinical specimens including blood, urine, sputum, stool, wound swabs, body fluids, and other samples.Perform microbiological tests such as Gram staining, culture inoculation, identification of microorganisms, and antimicrobial susceptibility testing.Prepare culture media, reagents, stains, and laboratory solutions as per standard protocols.Operate and maintain laboratory equipment including incubators, autoclaves, biosafety cabinets, microscopes, and automated microbiology analyzers.Monitor culture growth and record observations accurately.Ensure proper specimen storage, handling, and disposal according to laboratory and biomedical waste management guidelines.Maintain laboratory records, test reports, quality control logs, and inventory registers.Participate in Internal Quality Control (IQC) and External Quality Assurance Programs (EQAS).Follow infection prevention and biosafety protocols at all times.Report critical findings promptly to the Microbiologist or concerned clinician.Assist in outbreak investigations, surveillance activities, and infection control monitoring when required.Ensure compliance with NABH, NABL, and other regulatory standards.Qualification & Experience  B.Sc. Microbiology / Medical Laboratory Technology (MLT) / Life Sciences.DMLT with relevant microbiology laboratory experience may be considered.Additional certification in Clinical Microbiology is preferred.

Responsibilities               Assist in the preparation and submission of regulatory documents to health authorities for product registrations, including ANDAs/MAA/DCP/ANDS etc but not limited to these.Periodic tracking of evolving Global Regulatory updates and updating to team and implimentation of the new expectations of Global competent Regulatory Agencies and review of all relevant data inclusive of the Type II DMF/ASMF etc.Support the maintenance of regulatory files and databases, PLCM, ensuring accuracy and completeness of documentation.Collaborate with cross-functional teams, including Quality Assurance, R&D, and Manufacturing, to gather necessary information for regulatory submissions.Assist in the review of labeling and promotional materials to ensure compliance with regulatory standards.Participate in regulatory intelligence activities, including monitoring regulatory updates and communicating relevant information to internal stakeholders.Provide administrative support as needed, including organizing meetings, preparing meeting agendas, and documenting meeting minutes.Any other related duties as assigned by Project Leader                                            Qualification & Experience Currently enrolled in Master of Pharmacy degree program in Pharmacy, Regulatory Affairs, Life Sciences, or a related field.Strong attention to detail and organizational skills.Excellent written and verbal communication skills.Ability to work independently and collaboratively in a fast-paced environment.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).Prior experience or coursework in regulatory affairs or the pharmaceutical industry is preferred.

ResponsibilitiesDrive execution of defined workstreams within the business-analytics roadmap by demonstrating techno-functional consulting & stakeholder management capabilities, in close collaboration with data science & engineering SMEs and teamsStructure ambiguous business problems into clear analytical approaches, develop hypotheses, and translate them into actionable solution designs in partnership with the Engagement ManagerLead client discussions and working sessions on specific modules, presenting findings and recommendations with clarity and confidence in an evolving client environmentSynthesize analyses into compelling, insight-led recommendations and quantify how solutions and results improve clients’ objectivesPerform a role that combines hands-on analytical contribution with day-to-day management of a small team of associates, reviewing their work for quality and rigorContribute to organization building by mentoring associates and helping develop repeatable analytic approaches and reusable consulting assets Qualification & ExperienceBachelor’s Degree (BE / BTech - CS) from Tier I / II universities like IIT’s / NIT’s and MBA from Top Tier B-schools (IIMs) preferred.4-7 years of professional work experience in Pharma / Lifesciences analytics domains like HCP/HCO Segmentation, Brand Analytics, Omnichannel Marketing, Dynamic Targeting, Demand Planning, Pricing Management, Supply Analytics etc.Strong problem-solving analytical skills with an ability to blend creativity and logical thought to structure and solve complex problemsAbility to develop and articulate data-backed recommendations based on rigorous data analysisExperience in business / technology consulting roles conversant with process improvement, cost optimization, customer analytics and experience managementDemonstrated client-facing experience with the ability to manage stakeholder relationships and own workstreams at a working levelAbility to guide and review the work of junior team members

Responsibilities• You will be responsible for New Products conceptualization and planning by gathering feedback on unmet therapeutic needs, identifying new product opportunities, and presenting business cases to the vertical head and country head for timely product selection, aligning with long and short-term objectives.• You will be responsible for New Products Launch Planning by preparing product manuals, designing positioning strategies, and overseeing successful product launches through effective communication and collaboration with regional sales teams.• You will be responsible for Post-Launch Audit of New Products by coordinating with sales teams, reviewing performance, and initiating corrective actions when necessary to ensure new products meet or exceed sales projections.• You will be responsible for Branding and Promotions by conducting market research, finalizing positioning strategies, and overseeing effective promotion strategies by collaborating with ad agencies and implementing marketing plans in alignment with business goals.• You will be responsible for Continuing Medical Education (CME) Programs by identifying CME needs, inviting speakers and doctors, and ensuring successful execution of CME programs to establish lasting relationships with healthcare professionals.• You will be responsible for leading and developing the team by conducting performance appraisals, mentoring team members, and collaborating with HR for recruitment and talent development to maximize team performance and retention.• You will be responsible for sales planning and review by gathering feedback from regional sales manager (RSMs), devising region-specific strategies, and incorporating regional needs into the product plan to enhance overall performance.Qualification & Experience   • Educational qualification-A graduate degree in any Science stream • Minimum work experience- 7-10 years of experience in Product Management in pharmaceutical marketing especially with CVAD experience.• Understanding of Indian Pharmaceutical industry- competition, customer behaviour and prescription habits.• Strategic mindset to develop and implement long-term product strategies that align with the company's overall business objectives.• Analytical skills to assess market trends, competitor activities, and customer needs for the products in the portfolio.• Financial management skills to develop and manage budgets, allocate resources effectively, and optimize cost control for the product portfolio.• Excellent communication skills to convey complex scientific and medical information to diverse audiences, including healthcare professionals, internal teams, and stakeholders.• Ability to analyze market data, clinical trial results, and sales performance to inform decision-making and product portfolio strategies.• Ability to adapt to changes in the pharmaceutical market, including advancements in therapies, healthcare policies, and regulatory updates.• Proactive and visionary mind-set• Strong networking skills• Effective people management abilities• Adaptability and change management skills• Strategic orientation and decision-making capabilities

ResponsibilitiesBiobank OperationsManage end-to-end biobank activities including specimen collection, accessioning, processing, cataloguing, storage, retrieval, and distribution.Ensure specimen integrity through proper storage conditions, environmental monitoring, and temperature control.Maintain complete traceability of biological samples using Laboratory Information Management Systems (LIMS) or equivalent platforms.Ensure proper documentation and chain of custody for all biological specimens.Laboratory OperationsOversee day-to-day laboratory operations and ensure uninterrupted workflow.Manage preventive maintenance, calibration, validation, and troubleshooting of laboratory equipment.Coordinate with vendors for timely servicing and maintenance of laboratory infrastructure.Ensure laboratory equipment operates efficiently with minimal downtime.Quality & Regulatory ComplianceDevelop, implement, and periodically review Standard Operating Procedures (SOPs).Ensure compliance with GLP, GMP, GCP, NABL, FDA, HIPAA, GDPR, institutional policies, and applicable regulatory requirements.Lead internal audits and coordinate external inspections and accreditation activities.Ensure compliance with biosafety, biosecurity, hazardous material handling, and biomedical waste management guidelines.Inventory & DocumentationManage laboratory inventory, biological samples, reagents, consumables, and critical supplies.Maintain laboratory documentation, equipment logs, quality records, and audit documentation.Ensure data integrity, confidentiality, and secure management of research and patient-related information.Research CoordinationCollaborate with clinicians, researchers, Principal Investigators, and cross-functional teams to support research programs.Coordinate specimen logistics while ensuring compliance with approved research protocols.Support research initiatives by maintaining operational excellence within the laboratory.People ManagementTrain, mentor, and supervise laboratory and biobank personnel.Promote a culture of quality, safety, compliance, and continuous improvement.Monitor team performance and ensure adherence to laboratory standards and SOPs.Qualification & Experience   Strong knowledge of biobank operations and laboratory management.Experience with Laboratory Information Management Systems (LIMS).Thorough understanding of laboratory quality standards and regulatory guidelines.Knowledge of biosafety, biosecurity, and biomedical waste management.Excellent analytical, organizational, and documentation skills.Strong leadership, stakeholder management, and communication abilities.Ability to manage multiple priorities in a research-oriented environment.High level of integrity, attention to detail, and commitment to quality.Qualification : M.Sc./M.Tech./Ph.D. in Life Sciences, Biotechnology, Biomedical Sciences, Molecular Biology, or a related discipline.Certification in Quality Management Systems, Biosafety, or Laboratory Quality Management will be an added advantage.

ResponsibilitiesReceipt, evaluation and logging of complaints into TrackWise.Receipt, evaluation and logging of customer queries.Coordinate with internal & external stakeholders involved in the complaint handling process.Provide the acknowledgement and the response letter to the complainant.Reconciliation of received Product Quality Complaints.Qualification & Experience B.Pharma / M.Sc (Life Sciences)5-6 Years

ResponsibilitiesOversee the qualification, documentation, and traceability of Master and Working Cell Banks (MCB/WCB).Ensure compliance with GMP, EU Annex 1, and ICH guidelines for cell bank handling, storage, and distribution.Review and approve cell bank-related protocols, COAs, and characterization reports.Monitor environmental conditions and alarm systems for cell bank storage units (LN2 tanks, freezers).Support audits and regulatory inspections by providing cell bank documentation and responses.Coordinate with manufacturing, QC, and regulatory teams to ensure cell bank readiness for production.Manage deviations, CAPAs, and change controls related to cell bank operations.Issue Work Cell Banks (WCB) and Master Cell Banks (MCB) as per requirements.Batch Production Record (BPR) Review & DocumentationReview executed Drug Substance (DS) BPRs and associated documents for all products.Ensure timely deposition of reviewed documents to the DCQA.Qualification & Experience  Educational qualification: M.sc (Life Science) /M Pharm Minimum work experience: 4-8 years of industrial experience with specific operational experience in Quality Assurance and Manufacturing (Biosimilars

Responsibilities• Achieve assigned activity goals and targets for the territory as agreed with the reporting manager, with an initial high level of supervision and coaching provided by the company, customer and manager.• Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call.• Promote and sell customer’s therapeutic products to general practitioners, other identified healthcare providers, and/ or other healthcare professionals in the retail market.• Within a specific geographical territory, identify target customers while maintaining and analyzing customer records.• Maintain records in the reporting systems within the required timescales.• Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily calls.• Organize and hold group events to optimize business while complying with relevant country legislation.• Keep Line Manager informed about changes in competitor activities and other market changes.• Maintain an up-to-date sales / technical knowledge of specialty and disease areas and relevant publications as per customer profile.• Keep all Company equipment safe and in a good state of repair.• Share experiences, ideas and techniques in order to assist with the sales training of colleagues.• Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager.• Successfully complete career development courses and additional training as required by the customer.• Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines.• Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice• Perform other duties as assigned.Qualification & Experience• High School Diploma or equivalent 5 years’ relevant experience Req Or• Bachelor's Degree Life Sciences or related field Req• Equivalent combination of education, training and experience may be accepted in lieu of educational requirements Req• Basic knowledge of Pharma Market and related procedures.• Fluency software operating systems, such as MS Office and customer relationship management systems.• Effective verbal and written communication skills.• Ability to conduct face to face presentations to customers.• Ability to prioritize and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers, managers and clients.• Make plans to obtain any industry qualifications essential to function as a Medical Representative in the relevant market. Req• AZDL - Driver Licence - Valid And In State Req