ResponsibilitiesAssist in conducting clinical and departmental quality audits. Support NABH accreditation activities and compliance monitoring. Collect, compile, and analyze quality indicators and audit data. Participate in patient safety initiatives and quality improvement projects. Monitor adherence to hospital policies, protocols, and standard operating procedures. Assist in documentation, report preparation, and record maintenance related to quality activities. Coordinate with various departments for corrective and preventive actions (CAPA). Participate in surveys, inspections, and accreditation assessments. Support training and awareness programs on quality and patient safety.  Perform other quality-related assignments as delegated by the Quality Executive.

ResponsibilitiesQuarterly Investor Communication: Lead the preparation of quarterly investor presentations and press releases. Ensure financials, disclosures, and messaging are accurate, consistent, and fully compliant with regulatory requirements Pre-Quarter Analysis & Consensus Tracking: Support the preparation of pre-quarter Investor/ Analyst FAQs and maintain pre and post-results consensus tracking Competitive Intelligence & Insights: Develop comprehensive competitor deep-dive dashboards and presentations. Deliver both quantitative analysis and qualitative insights to support management decision-making Investor Engagement Support: Support execution of roadshows, conferences, and investor meetings through preparation of presentations and FAQs. Maintain consistent engagement with key stakeholders across the investor ecosystem Investor & Analyst Interface: Ensure timely, accurate, and well-articulated responses aligned with company messaging for analyst/ investor queries Shareholding Analysis & Engagement Strategy: Monitor weekly shareholding patterns and identify key trends. Use insights to structure targeted investor engagement strategies aimed at optimizing shareholder mix and value Investor Feedback & Market Perception Tracking: Capture and synthesize feedback from investors and analysts post interactions. Highlight perception gaps, key concerns, and valuation drivers, and feed insights into internal strategy and communication planning Investor Benchmarking: Conduct periodic benchmarking against peers on shareholding profile, analyst coverage, and valuation positioning. Identify gaps and recommend actions to strengthen investor positioning Data management & Tracking: Maintain investor database, analyst coverage tracker, and IR calendar. Ensure timely updates to IR website and disclosures. Build robust internal trackers for investor interactions and follow-ups

ResponsibilitiesCarrying out effective field work to achieve and surpass the assigned budget by generation of prescriptions through medical professionals (HCPs). Carrying out the effective RCPA and entering the correct information in the system and prepare / set objective (Pre Call Planning) for every Doctor call. Demonstrate and promote products to HCPs (doctors and pharmacists) as per the guidelines provided by the division to generate maximum prescriptions. Ensure regular customer conversion, no prescriber loss by following the division strategy by building effective relationship. Ensure the sufficient availability of the products at the pharmacists to honor the Doctor prescription and do the required number of POBs as per the division norms. Create / update the effective Doctor / Chemist list as per the division guidelines. Ensure the success of new launches by implementing the strategies suggested by the division. Managing distribution channel members such as Stocki

ResponsibilitiesAccountable for developing regional operational strategy for assigned clinical studies. Contribute to the translation of CDP into an optimal operational strategy and plan. Lead assessment of various scenarios operational for optimal execution of CDP. Collaborate with key investigators to reflect feasible and realistic operational inputs to CDP and ensure timeline and quality of studies meet the needs of CDP. Provide subject matter expertise and operational input into protocol synopsis and protocol, obtaining opinions in terms of study execution from key investigators, as appropriate. Challenge study team to ensure that operational feasibility, inclusive of patient and site burden and that timelines meet the needs of CDP. Validate budget and ensure impacts are adequately addressed. Participate in site selection process, with a focus on providing country insights, and therapeutic expertise to ensure alignment between study execution plan and program strategy. Responsible for clinical study budget planning and management, and accountable for external spending related to clinical study execution. Works closely with relevant stakeholders (strategic CRO partners, other vendors, CSM, COPL, and Program Management, Outsourcing, and Finance) to ensure the accuracy of budget spending on a regular basis. Oversee strategic CRO partners and other vendors to ensure the overall operational execution and delivery of the assigned clinical studies in compliance with quality standards (including ICH GCP, local regulations and Takeda SOPs), on schedule and on budget. Oversight includes but is not limited to Review and approval of key risk-based monitoring documents/plans, periodic review of outputs, decisions, and actions related to risk-based monitoring. Documented review and monitoring of issues, risks and, decisions at the study level. Support the identification of trends across sites and/or the study. Review and provide clinical operations expertise into clinical documents related to the drug development process Creation and maintenance of clinical trial materials, such as Investigator Brochures, study synopsis & protocols, clinical study reports, etc. Preparation of key regulatory meetings, as appropriate. Collaborate with cross-functional counterparts and strategic CRO partners/other vendors to ensure inspection readiness and lead Clinical Operations aspects of inspection readiness activities and act as subject matter expert during regulatory inspections.Qualification & ExpeirenceBachelor’s Degree or international equivalent required, Life Sciences preferred. Innovate and challenge peers and teams to think and work differently; Work independently, excel at solving issues without the need for support, but is effective at enlisting support for specific asks when necessary. Participate and lead clinical operations in cross-functional initiatives and workstreams that affect clinical operations; Adapt ways of working to the function’s current state and formulate strategic plans to work within the existing framework. Capable of assessing gaps cross-functionally and can take a supportive role in leading changes that benefits the function as it related to clinical trial execution and study management.

ResponsibilitiesManage and lead preparation, submission, and tracking of CTAs, substantial/non-substantial amendments, notifications, and other required submissions to Indian Health Authorities (CDSCO) as applicable. Ensure timely, complete, and compliant responses to HA questions/deficiency letters to prevent avoidable approval delays. Drive readiness and coordination for HA meetings/interactions, including SEC briefing preparation, Q&A preparation, and stakeholder alignment. Provide regulatory guidance to study teams on India clinical trial requirements, expectations, and risks; translate requirements into actionable submission plans. Oversee regulatory compliance monitoring during study conduct, including compliance with regulatory commitments and conditions of approval. Closely cordinate with the Global/International Regulatory Clinical Trials team, GDO, India R&D, Medial team and external partners (e.g., CROs) for regulatory afairs stregies on Clinical trials in India. Provide regulatory consultation and guidance to cross-functional study teams on Indian clinical trial requirements, expectations, and risks; translate requirements into actionable submission and mitigation plans. Monitor, analyze, and communicate regulatory intelligence related to Indian regulations, guidance, and evolving HA/SEC expectations; assess impacts on the pipeline and studies, and recommend actions. Support policy advocacy activities by providing technical and regulatory input, supporting position development, and engagement planning (as appropriate) with industry forums/associations and external stakeholders to help shape a favorable clinical trial regulatory environment.Qualification & ExpeirneceBachelor’s degree in Pharmacy, Life Sciences, Medicine, or related field (advanced degree preferred). Minimum 5 years of experience in pharmaceutical industry or CRO for managing regulatory affairs for Clinical trial in India. Demonstrated experience in clinical trial regulatory affairs in India, including CTA submissions and amendments.

ResponsibilitiesSets, Operates and monitors primary packing machines such as Pharmapack, CVC, Parle makes and associated machines like unscrambler, canister filling, cotton inserters and conveyors Ensure calibration of balances, correct machine settings, batch start up and challenge and inprocess checks Performs minor troubleshooting of packing machines Quality Compliance Perform in process checks like bottle quality, tablet appearance, counting accuracy, etc as per BPR Monitor rejections and ensure minimal rejection and losses during batch run Carry out cleaning activities and line clearance as per SOP before and after batch Maintains hygiene and discipline in packing area Documentation and Compliance Maintain accurate and timely records for BPRs and log books including equipment usage logs Report deviations, machine malfunctions or breakdowns to supervisors promptly Fills BPR and logbooks online during start up and while in operation for in process. Assists in reconciliation and rejections of in process and finished bottles. Teamwork and Coordination Coordinates activities of contractual staff for smooth functioning of line Train junior operators, contractual as and when requiredQualification & ExpeirneceITI, Diploma in Pharmacy, Diploma in Engg, B.sc. Total experience of 4 - 7 years in Operation of Packing Machine. Must be able to work in shifts as needed

ResponsibilitiesProvide subject matter expertise to teams to develop global strategies for the disclosure of clinical documents in accordance with applicable regulatory requirements. These requirements include, but are not limited to, EMA Policy 70, EU Clinical Trial Regulation, Health Canada Public Release of Clinical Information Guidance, and pertinent company policies/SOPs. Manage planning and preparation activities for disclosures. Drive quality in information, consistency across disclosures and related areas (eg, publications and data sharing), and completion of disclosures in a timely manner. Oversee vendors assigned to disclosure deliverables. Forecast and track outsourced disclosure deliverables. Act as the Pfizer point of contact to vendors, develop performance metrics, and participate in governance meetings. Promote open communication regarding project status and issue resolution. Lead development of standard processes and/or implementation of technologic solutions to enable compliance with disclosure requirements. Represent Medical Writing on clinical trial disclosure governance committees. Contribute to development of core expertise in disclosure and related fields within Medical Writing group by maintaining knowledge of regulatory guidelines and requirements as well as industry trends and best practices.Qualification & ExperienceAt minimum Bachelor's degree or equivalent in medical-related field or life science. Post-graduate degree preferred. BS/BA with extensive experience, MS/MA with strong experience, PhD with strong relevant experience in the pharmaceutical or biotech industry. Experience with regulatory medical writing and preparation of EMA Policy 70 submissions required. Knowledge of data and/or document anonymization strongly preferred. Excellent project management skills to organize work and handle multiple projects at the same time. 

Responsibilities Financial Analytics & Forecasting Design, develop, and deploy advanced machine learning models to forecast key business KPIs including expense allocation and cash flow management. Build automated business process optimization model and reporting systems using AI. Design variance analysis frameworks to identify key drivers of financial performance. Conduct scenario analysis and sensitivity modelling for strategic initiatives. Present findings and recommendations to senior leadership and stakeholders. Establish data quality standards and governance frameworks for financial analytics.Qualification & ExperienceBachelor's degree in Computer Science, Information Technology, or related technical field (required). Nice to Have Experience with healthcare industry-specific challenges with FP&A domain Knowledge . Experience with financial systems (SAP, Oracle, workday, or similar). Hands-on expertise in building autonomous AI agents and implementing the Model Context Protocol (MCP) for seamless data-tool integration.

Responsibilities Preparation of various master documents required for the submission batch execution and supports the product development by preparation of documents like master production records, Master Packing records and various reports like Exhibit Batch Summary Reports, Hold Study reports, Photo stability Reports, Transportation worthiness study report, Bulk product Stability Reports, SOPs and other miscellaneous reports. Responsible for Maintenance & updating of proper inventory of all the change parts and accessories for the equipments and Instruments. Indenting the punches, dies & machine change parts for the development and submission batches. Issuance of Logbooks for the new equipments, instruments, punches and dies. Preparation of Purchase indents in SAP for the procurement of raw and packing materials. Supporting the other sub-ordinates in learning of the equipments, system and process. Perform all work in accordance with established regulatory, compliance and safety requirements. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned related to Docuemntation & change controlQualification & ExperienceUniversity / College degree in Chemistry, Pharmaceutical Technology, or related science preferable B. Pharm/ M Pharm (Pharmaceutics) Knowledge, Skills and Abilities Should have good communication knowledge of English (Speaking, Reading and Writing). Should have skills in Microsoft Word, Excel and working knowledge in SAP. Knowledge of the Pharmaceutical manufacturing Process and cGMP is desirable. Should have the attitude of performing the allotted activities in compliance with all the established procedure with an aim to develop Quality Pharmaceuticals. Should take ownership for quality in the job, support our corporate values of Collaboration, Courage, Perseverance, and Passion. Experience Should have minimum 5 years experience in Technical Writing in the pharmaceutical industry/ GMP environment and overall 8-10 years working knowledge of Formulation Development, Manufacturing process in pharmaceutical industry.

Responsibilities Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report.  To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc.  Ensuring data integrity policy, GDP and its effectiveness up to compliance  To maintain the stability chamber and tracker.  To maintain the stability chamber and tracker.  To ensure charging and withdrawal of stability samples as per approved protocols.Qualification & ExperienceEducation :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.