Qualification & Experience Eligibility: Students pursuing a degree in Dietetics & Nutrition Limited Seats Available: Selection on a first-come, first-served basis

Qualification & Experience Required an Experienced MBBS Senior Resident for the Department of Cardiology, Plastic Surgery, Radiology & Obs Gynae.Qualifications MBBS, MD / MS

Qualification & Experience Eligiblity : MBBS Experience : 0-5 yrsresponsibilities of RMO includes Supervision of in-patient and out-patient care, Emergency response, Supervising junior doctors and nurses, Providing seamless coordination, etc.

Qualification & ExperienceQualification MS / MD / DNB in OBG Experience 2 - 5 years

ResponsibilitiesHandle inbound and outbound calls, document them, and perform follow-up calls as per client requirements and SOPs. Ensure compliance with Vizen Lifesciences and client quality requirements. Send completed documents for QC in hourly reports. Follow telephone etiquette in the MICC process. Refer to safety reference and client-provided documents while handling calls. Manage test calls, faxes, voicemails, and emails. Categorize call information into product complaints, AE/SAE, medical queries, and product quality complaints. Forward AE/SAE information to the pharmacovigilance department and product complaints to the QA department as required. Contact manufacturing units or clients regarding medical inquiries with unavailable information. Adhere to administrative, technical, and physical safeguards to protect all data, ensuring confidentiality, integrity, and availability. Handle respective trackers and perform reconciliation. Ensure adherence to client-specific SOPs for all activities. Attend training and client meetings as needed. Provide feedback and training to team members. Archive pharmacovigilance documents.Qualification & ExpeirenceBachelor's or Master's degree in Pharmacy or Nursing. Experience required: 0 to 15 years of relevant experience in Medical Information Call Center (MICC) Team Leads and ,Quality Reviewer positions require additional leadership or quality review experience

Responsibilities Triage incoming reports for completeness, legibility and validity  Bookin and Data entry of case reports into safety database  Request follow-up and perform query management  Coding of data in the safety database  Writing case narrative.  Perform Literature searches  Participate in client meetings as required  Preparation for, participation in, and follow-up on audits and inspectionsQualification & ExpeirenceQualification: B.Pharm/M.Pharm/Pharm D Experience: 1– 3 years

Responsibilities Draft PADER aggregate reports as per the aggregate reporting schedule. Prepare line listings and tabulations for inclusion in the PADER report. Develop and maintain the PADER report calendar and schedule. Coordinate and resolve queries with cross-functional teams before finalizing line listings, addressing any issues identified in draft cases. Communicate with cross-functional teams to obtain required inputs and resolve queries efficiently. Archive all PADER-related information in the designated shared drive. Submit PADER documents and reports within specified timelines, ensuring compliance with internal and regulatory submission requirements. Prepare and review SOPs and work instructions in alignment with ICH-GCP, GVP modules, and FDA guidelines. Provide training to junior associates on PADER report preparation and processes. Support client audits and regulatory authority inspections as needed. Qualification & Experience4–6 years of experience in aggregate report preparation for quality control roles. 3–4 years of experience in aggregate report drafting roles. Educational Qualifications M.Pharm or Pharm.D candidates are preferred.

ResponsibilitiesReview external GMP batch documentation from CDMO partners for completeness, accuracy, and compliance with approved manufacturing and regulatory requirements. Evaluate analytical data, Certificates of Analysis (CoA), and laboratory documentation to ensure data integrity and GMP compliance. Support Quality oversight of external manufacturing activities, including preparation for batch disposition. Identify documentation inconsistencies, deviations, and potential compliance risks, ensuring timely escalation to Quality stakeholders. Collaborate with internal teams (QA, QC, Supply Chain) and external CDMO partners to resolve documentation queries and ensure alignment. Generate and maintain Key Quality Indicators (KQIs) to monitor external manufacturing quality performance. Ensure adherence to Lonza Quality Standards, data integrity principles, and global/local GMP regulations. Qualification & ExpeirenceBachelor’s degree in Chemistry, Biotechnology, Pharmaceutical Sciences, or related field. Experience in GMP-regulated pharmaceutical, biopharmaceutical, or CDMO environments is advantageous. Understanding of GMP documentation, batch records, and data integrity requirements.

Responsibilities Global Service Oversight: Manage workload, priorities, and resource planning across a global service model.  Document Lifecycle Management: Oversee end-to-end document lifecycle processes (creation, review, approval, effective, archival) ensuring timely and compliant execution.  Compliance: Ensure adherence to GxP requirements and Good Documentation Practices (GDP/ALCOA+).  System Administration: Ensure effective operation of the eDMS (e.g., Veeva), including workflows, templates, and metadata structures.  Performance Monitoring: Define and monitor KPIs (cycle times, right-first-time, data accuracy), analyze trends, and drive improvements based on insights.  Reporting: Provide regular reporting to leadership on system performance and compliance metrics.  Training & Capability Building: Ensure team and users are trained on eDMS processes and GDP requirements. Build team capability to deliver services across global stakeholders and time zones.  User Support: Oversee the global DMS user support request process (F11 requests) and provide guidance to document authors and users.  Continuous Improvement: Identify and lead implementation of process improvements and system enhancements to increase efficiency and compliance.  Global Super User Role: Act as global administrator of the eDMS, managing ownership of documents, workflows, and metadata.  Approval Gatekeeper: Act as the final approver for global documentation during approval workflows, ensuring compliance with administrative rules.  Cross-Functional Collaboration: Manage review and approval workflows across QA, Manufacturing, QC, Engineering, and Regulatory Affairs.  System Transition Support: Support cleanup activities and preparation for new eDMS implementations.  Other Duties: Perform additional tasks as required to support global quality systems. Qualification & Expeirence Bachelor’s degree or higher in Chemistry, Biochemistry, or Pharmacy. Experience & Skills  Experience with Quality System Management in GMP-regulated environments.  Background in (Bio)pharmaceuticals or similar highly regulated industry.  Self-starter with solution-driven mindset.  Strong communication and influencing skills in international environments.  Project management experience is a plus.  Green Belt certification is a plus. 

Responsibilities Manage end-to-end supplier quality processes including Vendor Change Notifications, Supplier Quality Agreements, supplier complaints, and Vendor Supply Chain Integrity activities to ensure timely and compliant execution.  Review, assess, and process supplier quality records and supply chain documentation to support material, service, and equipment qualification across the Lonza network.  Apply analytical and technical judgment to evaluate supplier requests, identify quality and operational risks, and determine appropriate actions to maintain compliance and supply continuity.  Coordinate cross-functional impact assessments with stakeholders including MSAT, QC, Manufacturing, Planning, and Procurement to ensure risks and required actions are effectively managed.  Maintain compliant supplier documentation, data integrity, and traceability within SAP, TrackWise, Document Management Systems and other enterprise quality systems.  Monitor supplier quality KPIs, support inspections and audits, and drive timely implementation of global supplier quality actions and process improvements.  Serve as a key point of contact for supplier quality processes by providing guidance, ensuring effective stakeholder communication, and supporting a culture of quality, collaboration, and continuous improvement. Qualification & Expeirence University degree in Biochemistry, Chemistry, Pharmacy, Microbiology, Biotechnology, or a related scientific discipline.  2–5 years of experience in Supplier Quality, Quality Assurance or Supplier Qualification within a regulated pharmaceutical, biotech, or life sciences environment.  Good understanding of cGMP, FDA, and supplier quality requirements related to VCNs, QAAs, supplier complaints, and supplier qualification processes.  Hands-on experience with enterprise quality systems and tools such as SAP, TrackWise, and Document Management Systems.