ResponsibilitiesLead end-to-end regulatory activities for innovative biological product portfolios across global markets (Emerging Markets).Develop and execute regulatory strategies aligned with business objectives and market requirements.Oversee preparation, review, and submission of dossiers (CTD/eCTD) including IND/IMPD/CTA, MAA, variations, amendments, and renewals.Act as the primary point of contact with country affiliates and global health authorities for regulatory interactions, queries, and inspections.Provide strategic guidance on regulatory pathways for biological products including clinical requirements of country of origin or single region clinical study data.Ensure compliance with evolving regulatory frameworks, guidelines, and quality standards.Collaborate with partners and cross-functional teams (R&D, Quality, Clinical, Medical, Manufacturing, commercial, marketing and supply Chain) to drive regulatory milestones.Identify risks in submission timelines and proactively implement mitigation plans.Qualification & Experience Advanced degree in Pharmacy, Biotechnology, or related field.Strong experience in Regulatory Affairs with exposure to biosimilars or biologicals.Proven experience in handling global submissions (ANVISA, SAHPRA, DIGIMED, TGA, MEDSAFE, COFEPRESS,USFDA, EMA, or other major agencies).Strong understanding of biosimilar regulatory frameworks and lifecycle management.Excellent communication, strategic thinking, and stakeholder management skills.Regulatory Strategy & ComplianceGlobal Stakeholder ManagementAnalytical & Problem-Solving SkillsStrong Execution & OwnershipEducational qualification: Post graduate in Pharmacy/ScienceMinimum work experience: 8+ years in Pharmaceutical Industry with 5 years of experience in global regulatory affairs.Experience in formulation development, analytical development and quality.Understanding of Good Manufacturing practice/Quality Systems.Understanding of product development, manufacturing processes, Intellectual Property and quality.Technical knowledge and understanding of the regulatory requirements of different dosage forms.Thorough understanding of regulatory guidelines for different countries, ICH guidelines, pharmacopeia's, product filing and approval requirements.

Responsibilities               Be a Subject Matter Expert in method development of HPLC and GC techniques.                                      Basic instrument operational skills.                                                 Qualification & Experience M .Pharm .        

Responsibilities               New Projects has been added in my group to handle that projects these man power is required.                                                          Qualification & Experience M. Pharma or M.Sc.   

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.

ResponsibilitiesAssist in the preparation and dispensing of medications.Maintain accurate records and documentation.Provide excellent customer service to patients and healthcare staff.Participate in quality improvement initiatives.Collaborate with the pharmacy team to optimize patient care.Inventory and Supply Chain:Order and purchase pharmaceutical supplies, medical supplies, and drugs.Maintain stock levels and ensure proper storage and handling.Maintain inventory and Reorder Level (ROL).Place orders for medicine/consumables based on consumption trends.Ensure timely receipt and storage of ordered supplies.Qualification & Experience  Education: Bachelor's degree in any field.Training: Willingness to undergo in-house training as a Pharmacy Assistant.Excellent communication, interpersonal, and organizational skills.Ability to work accurately with minimal supervision.Ability to comprehend written instructions from doctors and other departmental personnel.Ability to plan and organize work schedule effectively.Strong speaking and listening skills to understand and carry out instructions.Ability to work in a team.Enthusiasm and open-mindedness.

Responsibilities• To develop pharmacy auditing tools.• To ensure smooth pharmacy operations at the facility.• To actively arrange for training of pharmacists/ team members.• To manage vendor or development – maintain relationship with vendors/ manufacturers.• To identify skill, competency levels of subordinates and work for continuous resource development.• To manage inventory – ensure availability of all stocks at pharmacy keeping the inventories low.• To ensure non-moving and expiry stock management.• To maintain update knowledge on new drugs and medical supplies.• To ensure compliance of pharmacy with licensing and certification needs.• To coordinate with physicians, advise and provide information on new drugs and products.• To regularly plan marketing / promotional activities for the department.• To ensure achievement of strategic objectives - revenue, cost and service.• To provide price and market linked information to MSD.• To ensure audit & compliance to Pharmacy laws & regulation.• To be well groomed, punctual & adhere to company policies and practices.• To have complete orientation of QMS and EMS system of Hospital.• To have complete Awareness about Disaster Management Programme (DMP) of the hospital.• To Comply with the service quality Process, environmental & occupational issues & policies of the respective area• To Comply with patient safety policy• To ensure safe utilization of equipment and proper waste disposal system.Qualification & Experience  • B Pharma D Pharma

ResponsibilitiesUnderstand the market and category opportunities within territory to identify opportunities for market share growth at the customer/account levelMaintain deep, current knowledge about medical and nutritional science, the evolving healthcare landscape, and emerging digital trends to support selling and educating a broad and deep network of HCPs about Abbott productsDevelop and execute on multichannel customer engagement plans that generate demand for Abbott brand product and grow recommendation and market shareLeverage information about customer segmentation, type and behaviors to inform customer engagement and account management strategiesDevelop and maintain strong relationships with HCPs throughout the customer account, at different levels of responsibility and influence using existing relationships with HCPs and others to expand customer networkSecure commitment to recommend Abbott products as the brand of choice by increasing HCP knowledge about the role and importance of nutrition on patient quality of life at key points throughout the patient care journey; and the role of Abbott’s products in increasing quality nutrition through consultative selling dialoguesDefine and deliver ‘Unique Value Proposition’ from the HCP’s perspective (including but not limited to the positioning of Abbott brand products) by continuously uncovering the needs and priorities of individual HCPs using multichannel touchpoints and engagement activitiesEffectively deliver a consultative sales call from the perspective of the HCP (and their patients) to expand HCP’s knowledge of nutritional interventions and the measurable benefits of Abbott brand products, anticipate and manage objections, and gain clear commitment to recommending Abbott products and other brand-building activitiesEstablish target customers and develop clear customer plans to achieve coverage, frequency and call rate objectivesImplement customer segmentation, identify new leads/customers and ensure timely reporting of daily activities as per the SFE SOPUse data and insights from digital and other omnichannel activities to refine HCP profiles and choose engagement activities that will fit the needs, preferences and goals of each individual HCPCollaborate with cross-functional teams (Marketing, SFE, CRM, etc..) to support patient education regarding nutrition and Abbott brands, to influence customer and patient choice of nutrition products, and deliver a consistent, end-to-end customer engagement experienceMeasure progress against customer and account objectives, per the account plan, and take action to ensure targets and KPIs are met (monthly, quarterly, annually) as assigned by the Sales ManagerAct in alignment with compliance and regulatory expectationsQualification & Experience Graduate - Medicine, science, pharmaceuticals/ nutritionMinimum of 1 years’ experience in Pharma/Nutrition IndustryUpto 5 years’ experience for Grade 12 and 5+ years’ experience for Grade 13Should achieve a 60% in the written testHas excellent product knowledge and is able to translate that knowledge into effective in-clinic performanceGood understanding of nutrition scienceAbility to establish connect and develop contacts and relationships, with easeKnows his numbers well and is an good team player collaborates where possible

ResponsibilitiesShould be capable of leading the team towards QMS elements which includes handling of deviations, OOS, market complaints, CAPA management, Risk assessments, change controls, protocols, reports, discrepancies, batch and packaging records closures.Driving the improvement projects in the drug product.Should be leading the team for All time audit readiness and should be writing the responses to audit observations.Reviewing and approving SOPs, protocols, reports, discrepancies, change requests, CAPA (Corrective and Preventive Actions), QRM (Quality Risk Management), and batch and packaging records.Collaborating with cross-functional departments to close discrepancies and implement corrective actions, ensuring compliance with relevant GMP (Good Manufacturing Practices), safety standards, and SOPs for designated manufacturing equipment.Completing batch documentation in compliance with GMP, collecting and maintaining data, and participating/leading in quality and safety investigations to address and improve CAPA for drug product manufacturing.Engaging in continuous improvement activities, adhering to safety rules, and reporting any unsafe matters or near misses/accidents."Qualification & Experience Minimum 10+ years of experience with qualification in B.Pharmacy/M.Pharmacy/B.Tech/M.Tech biotechnology 

Qualification & ExperienceDip. Pharm/B.Pharm 1+ years experience

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