ResponsibilitiesClinical responsibility:Performs triage on incoming patients to become part of the ER’s current loadOversees patient care, treatment, and recoveryParticipates in research efforts and clinical studiesMaintains clinical records in line with regulations and standardsClears patients for discharge or further procedures with specialistsConducts follow-up to monitor patient’s conditionResearchConduct medical research to aid in controlling and curing disease, to investigate new medications, and to develop and test new medical techniques.Be thesis guide for fellows, residents and PhD candidates.AdministrativeCoordinate and direct work of nurses, medical technicians and other health care providers.Inform students and staff of types and methods of critical care administration, signs of complications, and emergency methods to counteract reactions.Manage Critical Care services, coordinating them with other medical activities and formulating plans and procedures.TeachingMust take part in the ongoing teaching activities.Organize and attend workshops, seminars, conferences, CME’s at local, regional and national level.

ResponsibilitiesPlan and perform vendor qualification and audits for pre-clinical, clinical, and In-vitro studies service providersPost study audit (off-site and on-site) of Pre-clinical, Bioequivalence studies and Clinical studies.Maintain and update the Quality Management System for Global Clinical ManagementDevelop, review, and approve SOPs for pre-clinical, clinical, and QA processesExecute Clinical audit programs and support health authority inspectionsReview regulatory deficiencies and support cross-functional teams in preparing responsesAnalyse deviations, incidents, and root causes, implementing corrective and preventive actions for clinical studiesSelf-Inspection of Global Clinical Management teamThe ideal candidate will have a strong background in GCP, GLP, and quality management processes, with the ability to work efficiently in a fast-paced environment.Qualification & Experience   Master's degree in Pharmacy or Clinical research8-12 years of experience in clinical quality assurance or related fieldStrong proficiency GCP and GLPHands-on experience with bioanalytical analysisProven track record of working with large-scale data sets and data warehousingExcellent understanding of data governance principlesKnowledge of current Regulatory updates and InspectionsStrong analytical and problem-solving skillsAttention to detail and ability to work efficiently in a fast-paced environmentExcellent communication and collaboration skillsAbility to work independently and as part of a teamStrong organizational skills and ability to manage multiple projects simultaneously

Responsibilities Provide 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 & ExpeirenceAt 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. 

Responsibilities Monitor performance by close interaction with project leadership/functional leadership and ensure that ongoing/revised project documentation and correspondence is accurate and complete. May be responsible for own assignments as project team member. This may include but not limited to taking the role of a senior level contributor on a project team and ensuring high quality and timely delivery of own deliverables, generating study specific status reports for study teams, Sponsors and/or management, and attend project team meetings as required at the project level Provide consultation, facilitate metrics collection and develop action plans in conjunction with Management/Project Leadership/Leads to keep project on time and within budget. Manage and oversee team activities including appropriate resourcing of staff, staff assignments, quality control and efficiency of project deliverables Where assigned, produce accurate resourcing plans in conjunction with appropriate Project Team Members, including but not limited to facilitating appropriate resource identification and assignment, and monitoring resource needs throughout the project as needed.Qualification & ExperienceEducated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or relevant clinical other equivalent experience.

Responsibilities Determine plan of action for incoming calls; Collect, process, and track incoming adverse and serious adverse events; Write safety narratives; Report on various safety data; and Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.Qualification & ExperienceBachelor of Science in Nursing (BSN) or higher (MSc Nursing preferred) Clinical experience in a hospital or healthcare setting Proficient knowledge of Microsoft® Office; Broad knowledge of medical terminology; and Strong organizational and communication skills.

Responsibilities Assist in the preparation of Core Lab Data Management documents; Perform validation on data transfers and edit programs; Maintain data cleanup via edits, data review and data changes; and Send data transfers externally.Qualification & ExperienceBachelor's degree in life science/ pharmacy/ health related field with strong attention to detail and working knowledge of Excel and Word; and 1-2 years of experience in a pharmaceutical or CRO setting preferred.

ResponsibilitiesCath Lab Case Support: Prepare devices and perform valve crimping strictly in accordance with IFU guidelines; maintain sterile technique; and support procedural workflow as per physician and hospital protocols Customer Coordination: Address basic product and workflow-related queries; coordinate case scheduling and logistics with hospital staff and internal teams CT/Data Collection: Coordinate, collect, and securely manage CT scans and key planning data; ensure proper documentation and handover for case planning Supply & Payment Follow-ups: Liaise with hospital purchase and supply teams to ensure stock availability, track deliveries/GRN, and follow up on payment status; promptly escalate issues when required Product Awareness (Compliant / Non-Promotional): Facilitate product familiarization and support related logistics in alignment with company policies and regulatory guidelines Reporting & Documentation: Maintain accurate case logs, inventory usage records, and visit reports; complete all mandatory training and certifications within defined timelines Travel: Provide support across assigned regions and, when required, travel across India at short notice, including for urgent case supportQualification & Experience Bachelor’s degree in Pharmacy, biomedical engineering, Life Sciences or related field Advanced degree such as Master’s or MBA preferred

ResponsibilitiesLead and develop team of 7 Senior Associates across Clinical Customer Service, Logistics Vendor Management and Development Supply Chain Technologies. Define goals, manage performance, and support career development. Ensure appropriate staffing, cross-training, and succession planning. Foster a culture of accountability, compliance, and customer focus Drive adoption of new technologies and AI to increase team productivity and enhance performance Clinical Supply Chain Execution OversightEnsure efficient and compliant execution of assigned clinical supply chain processes with patient-centric mindset Closely coordinate issue triage and workload prioritization with global peers Monitor KPIs and overall team performance and drive corrective actions and learning when needed Provide guidance on complex operational matters. Ensure adherence to GMP, GDP, and regulatory requirements.Performance & Process ManagementEnsure procedures are current, compliant and inspection-ready Drive root cause analysis and continuous improvement. Represent the team during audits and inspections.Cross-Functional & Global CollaborationPartner with Global Clinical Supply Chain, Clinical Study Teams, Quality, Finance, and DTI. Translate global priorities into actionable local plans.Qualification & ExperienceBachelor’s Degree and 8+ years of supply chain, logistics, planning, or operations experience

Responsibilities Ensure all engineering activities are executed in compliance with cGMP, GEP, and site SOPs.  Ensure compliance with Quality Management Systems (QMS) and applicable regulatory guidelines.  Handle all quality documents related to engineering such as Change Controls, Deviations, CAPA, and Quality Risk Management.  Review and update the respective planner and ensure compliance of activity on time.  Prepare and revise SOPs for plant machinery, utilities, HVAC, and water systems.  Support preventive maintenance execution as per the defined PM schedule and SOPs.  Assist engineers in installation and commissioning of new equipment.  Ensure effectiveness of training through review, feedback, and improvement initiatives.  Draft and update Job Descriptions for department personnel based on roles and responsibilities. Act as the Training Coordinator for the Maintenance Department.  Update classroom/adhoc training records in training software.  Generate re-training requirements for SOP changes or compliance gaps.  Prepare, review, and revise training matrices as per SOP changes or department needs.  Identify and update training needs (TNI) and ensure compliance with training requirements.  Manage user creation/inactivation and credential sharing in AIMS software or equivalent systems.  Ensure new joiners are trained according to function mapping and training plan.  Upload training materials (new/revised SOP copies) and track completion.  Attend scheduled trainings and ensure personal and departmental training compliance.

Responsibilities Manage, control, and maintain all Quality Assurance (QA) documents, records, and logs in compliance with GMP requirements.  Ensure timely issuance, retrieval, archival, and destruction of controlled documents according to approved procedures.  Maintain document revision history and ensure only current, approved versions are available for use.  Coordinate document review, approval, and distribution processes with QA, Production, QC, and other departments.  Monitor compliance with document control procedures and support internal audits and regulatory inspections.  Maintain electronic and physical document management systems, ensuring data integrity and confidentiality.  Track periodic review schedules for Standard Operating Procedures (SOPs), specifications, forms, and quality manuals.  Support change control activities by updating and distributing revised documents as per approved changes.  Prepare document control metrics, reports, and status updates for management review. Qualification & ExperienceB. Pharm B. Pharm - Required M. Pharm M. Pharm - Preferred Experience: 2 years or more in 2 - 5 Years