ResponsibilitiesProvide scientific and medical support across the organization; develop and review medical content; support medico-marketing activities; ensure regulatory and promotional compliance; manage KOL interactions and medical queries; conduct literature research; and contribute to clinical and competitive intelligence.Qualification & Experience M.Pharm or Pharm D (Pharmacology); pharmaceutical industry experience.

ResponsibilitiesEnvironment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualification & ExperienceQualification: M.Sc (Microbiology) / B.Pharm Experience: 3-4 years EM monitoring in aseptic process area including Grade A,B,C and D

ResponsibilitiesClient Engagement & Delivery Leadership Lead end-to-end program delivery across multiple pharma accounts and workstreamsOwn project planning, delivery governance, execution tracking, and risk management Define timelines, delivery milestones, resource planning, stakeholder communication plan and change management strategies for delivered solution adoption within Client Org Manage senior client stakeholders and build long-term relationships Ensure successful delivery outcomes with high client satisfaction and business impactDrive program governance, issue resolution, and escalation managementTeam Leadership Manage and mentor engagement managers, analysts, consultants, and cross-functional teams Drive team performance, accountability, collaboration, and professional developmentFoster a high-performance and learning-oriented culture within the pharma group Pharma Practice & Capability Building Build and strengthen the pharma industry practice as a SME Develop reusable solutions, accelerators, frameworks, and best practices for pharma engagements Create case studies, capability decks, thought leadership content, and internal knowledge assetsConduct domain trainings and mentor teams on pharma business processes, analytics, and consulting approaches Support organizational capability building in commercial pharma, patient analytics, market access, engagement planning, and related areas Contribute proposal development, solution design, effort estimation, and storytelling for client opportunities Collaborate with cross-functional teams to create tailored solutions for pharma clients  Qualification & Experience11+ years of experience in consulting, analytics, pharma commercial operations, or life sciences industry Strong understanding of pharmaceutical business processes, in atleast one or more Business functions across pharma value chain – R&D, Market Access, Launch Planning & Execution excellence, Value and Pricing, commercial analytics, Customer (HCP) & Consumer (Patient awareness) engagement, patient analytics. Proven experience managing large-scale client engagements and delivery programsExperience in proposal creation, solutioning, and client presentations Strong stakeholder management and executive communication skills Demonstrated ability to lead cross-functional and distributed teamsExperience working with global pharma clients and senior business stakeholdersAbility to manage multiple priorities in a fast-paced environment Experience in one or more areas: AI, Data Science, Analytics, Technology Consulting, or Data Engineering  Strong understanding of analytics delivery models, data platforms, and enterprise solutioning Exposure to proposal creation, pre-sales support, and solution development is preferred for Analytics/DS/AI roles 

ResponsibilitiesTo ensure cGMP and compliance review in the manufacturing shop floor and packing areas. To supervision of dispensing activity of manufacturing shop floor and packing areas. To Issuance of Bottle label, Ouster and Medication guide for commercial batch. Rsponsible for providing machine and area clearance. To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol. Online Documents and records review like equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. Calibration of IPQA instruments. Additional Responsibilities Real-time Monitoring and Compliance Reporting. Participation in Investigations. Provide on-the-job training to shop floor personnel on GMP practices, quality standards, and documentation practices. Maintain IPQA-related documents and records in a state of audit readiness. To have good written and verbal communication skills in English language.Qualification & ExpeirenceBachelors Degree (BA/BS) B. Pharm - Required Experience  2 - 4 Years

Responsibilities Nonclinical safety and toxicology study design & execution -  Design, plan, and conduct in vivo and/or in vitro safety pharmacology and toxicology studies in alignment with GLP principles. Select appropriate species, study duration, and endpoints based on pharmacology, pharmacokinetics and regulatory requirements. Review study raw data, protocols, results and reports.  Oversee study execution, ensure data accuracy, and coordinate with CROs or internal cross functional teams. Risk Assessment & Safety Evaluation -  Analyse and interpret the safety and toxicology data and integrate findings with pharmacokinetics and pharmacodynamics to assess potential safety risks.  Perform toxicological risk assessments including PDE/OEL/ADI derivations, impurity/excipient qualification assessments, extractables & leachables evaluations, and safety margin calculations.  Conduct exposure assessments for process materials, impurities, metabolites, degradation products and excipients.  Regulatory & Documentation -  Prepare and review high-quality safety and toxicology study reports, technical summaries, and nonclinical sections of regulatory submission documents (IND, NDA/MAA, ANDA, eCTD Modules 2.4/2.6 & 4, briefing books and IB, etc.).  Support regulatory filings to USFDA, EMA, DCGI, and other global agencies.  Draft and review regulatory query responses, briefing documents, and expert justifications.  Toxicology Informatics & Literature Research -  Perform comprehensive literature searches using toxicity databases (e.g., PubMed, TOXNET, ECHA, HSDB, etc.,).Qualification & ExpeirenceMaster’s or PhD in Toxicology, Pharmacology, Veterinary Sciences, or related biomedical science discipline. 8-10 years’ experience in preclinical toxicology with at least 5 years as a Study Director in a GLP-certified facility.

ResponsibilitiesAchieve sales, volume, growth, market share and listing targets for assigned brands.  Plan, orchestrate and execute HCP engagements, aligned with MCCP by tailored Patient Focused Interactions using right content based on HCP needs & priorities.  Report customer engagement activities in Veeva CRM and take advantage of all available functionality for enhancing customer interaction and experiences.  Monitor and communicate competition activity to Managers (FLSM, Management) to reflect market dynamics and potential counteracts.  Organize / Set-up regular scientific updates (e.g. CME, Scientific meetings) for HCP groups in alignment with defined marketing strategies.  Self-develop on latest medical/clinical knowledge, brand strategy and tactics, competitive landscape and standard platforms in order to challenge the status quo.  Collaborate with and provide feedback to Sales / Marketing on MCCP strategies and tactics and identify potential new sources of business.  Comply with local regulations, industry, and company policies and code of conduct.  Distribution Management: Collection of SSRs; Collating Primary vs Secondary sales; Collection of Orders from distributors; Adhering to the sales Credit Policy; Ensuring Phased distribution of orders such that he completes 40% targets by 15th of every month.  Qualification & Expeirence Bachelor’s Degree in any discipline (Any advanced qualification is a plus).  Minimum 2 – 3 years of pharmaceutical sales experience with a demonstrated performance track record.  Strong interpersonal, communication and team skills  IT literacy (basic knowledge and skills to utilize computers/tablets and related technology efficiently)  Excellent command (both oral and written) of local native language  English language skills are a plus  Energetic, Enthusiastic, self-driven, organized & willing to work extensively in field 

ResponsibilitiesPlan, perform and document scientific experiments in the laboratory for drug substances (DS) and drug products (DP) in collaboration with multifunctional project teams. Contribute to maintenance of lab instruments/day-to-day operations. Timely execution of project related activities. Plan, organize, execute, and document scientific experiments (e.g., analytical method developments/ validations/ transfers/ stability/ release testing, formulation development analytics etc.) according to the agreed timelines and appropriate quality standards. Accountable for documentation and submission of raw data in appropriate data system (for e.g., LIMS test activation and results entry). Accountable for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities. Support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls as needed. Responsible for implementation and maintenance of lean/efficient/environmentally sustainable practices in the laboratory. Proactively communicate key issues and any other critical topics in a timely manner to the manager and/or to any other relevant project team member(s). Responsible to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities. 

Responsibilities• You will be responsible for serving as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy.• You will be responsible for conceptualizing and managing a wide range of medical activities, aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs.• You will be responsible for engaging key thought leaders through medical affairs activities, in line with the overall strategic plan.• You will be responsible for ensuring the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects.• You will be responsible for acting as a therapeutic area scientific expert, discussing scientific data with leading specialists, and providing training on the latest medical developments to the sales and marketing team.Qualification & Experience  • Educational qualification-MBBS with M.D. Pharmacology/Medicine or full time post-graduate qualification in any discipline of medicine??• Minimum work experience- 2-4 years of experience in the pharmaceutical industry or research company in a Medical Advisor capacity.• Training in medical writing, clinical trial methodologies, research design and ICH – GCP will be added advantage• Must have working knowledge of Indian regulations pertaining to Health care professional’s interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals• Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data• Strategic mind set with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship is essential• Experience with complex business environments preferred• Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards

ResponsibilitiesTo Work in shift operation as per production schedule.Responsible to configure, deploy, and support MES applications.Create and maintain Electronic Batch Records (EBR), master recipes, workflows, and system parameters.Perform MES change management including configuration changes, upgrades, and patch installations.Ensure MES compliance with GxP, 21 CFR Part 11, EU Annex 11, and ALCOA+ principles.Support CSV activities including URS, FRS, DS, IQ, OQ, PQ, and risk assessments.Participate in internal and external audits and inspections related to MES.Prepare and maintain SOPs, work instructions, configuration specifications, and technical documentation.Conduct MES training for shop?floor users and system administrators.Support deviation investigations, CAPAs, and change controls related to MES.Identify opportunities for process automation, paperless manufacturing, and digital maturity improvements.Drive MES performance optimization and best practices adoption.Support data analytics and reporting initiatives for manufacturing KPIs.Qualification & Experience  4–8 years of experience supporting or implementing MES in a pharmaceutical, biotech, or regulated manufacturing environment.Hands?on experience with manufacturing processes (e.g., formulation, filling, packaging).Experience working in GMP and validated system environments.Strong knowledge of MES.Experience with SAP integration, automation systems (PLC/SCADA), and databases.Strong analytical and problem?solving skills.Excellent communication and cross?functional collaboration abilities.Ability to work independently in a fast?paced manufacturing environment.Strong documentation and stakeholder management skills.

ResponsibilitiesLiterature Management Process Perform review of literature results retrieved and imported into literature citation management system on a weekly basis and determine if minimum criteria for ICSR is met for marketed products Perform review of literature results to determine if article contains new aggregate safety information in support of the periodic report and/or signal detection Determine whether full text article needs to be ordered and order them if further information is needed to confirm if citation meets criteria for ICSR or for signal detection Flag articles containing new aggregate safety information for TA Safety to perform secondary review Request Local Safety Officer to provide English translation if the article is not in English Notify business partner of articles received, if applicable Support audits and inspections Knowledge And Skills Ability to identify literature articles containing ICSR criteria or aggregate safety findings supporting signal detection Ability to order full text articles where needed Ability to receive feedback from Case Management and TA Safety and optimize quality of literature review Demonstrate knowledge of global aspects of pharmacovigilance Strong knowledge of processes and global regulations for pharmacovigilance and literature surveillance Ability to effectively manage competing priorities and timelines Strong knowledge of literature citation management systems and platform used to configure search strategies Experience in use of AI and prompts would be usefulQualification & ExperienceMaster’s degree and 1 year of pharmaceutical, biotech or regulatory authority experience in a research and development setting OR Bachelor’s degree and 1- 2 years of Literature screening/Review or relevant Safety experience