Qualification & Experience           Department : Psychiatry          Qualification : UG - MBBS, PG - Psychiatry             Experience : Fresher           

Qualification & Experience      Department : Orthopaedics        Qualification : UG - MBBS, PG - OrthopaedicsExeperience : one year completion of Senior Resident 

Qualification & ExperienceMBBS, MD, DNB (General Medicine) Experience: Minimum 3 years and above

Qualification & ExperienceMBBS, MD, DNB (Gastroenterology) Experience: Minimum 3 years and above

Qualification & ExperienceMBBS, MD, DNB (Radiology) Fresher / Experienced

Qualification & ExperienceBUMS/BAMS/BHMS/MBBS Experience: 2-5 years

ResponsibilitiesThe Associate Manager will develop with support and supervision, relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content. Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content. Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.).  Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content. Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content.  Track the progress of projects and resolve any issues/problems with guidance from manager.  Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry.    Qualification & ExperienceAdvanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD) 2+ years experience in pharmaceutical medicine, including medical affairs, medical compliance. Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc.  Strong interpersonal skills to quickly build rapport and credibility with colleagues and key external stakeholders cross culturally/regionally.  Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.  Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings  Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development  

ResponsibilitiesOverall responsibilities for quality assurance compliance at the Zydus Hospira Oncology Private Limited (ZHOPL) site and Pfizer Quality at & ensure sustainable GMP compliance for Pfizer Products manufactured at ZHOPL site as per Quality agreement.Batch record review and release authorization compliance functions:Responsible for review and authorize the packed batch lot(s) for distribution in respective market from ZHOPL.To be part of SQRT as needed for any Batch related issue discussion.Regulatory impact assessment for all types of change related to Pfizer productsResponsible for Review and approval of Change controls at ZHOPL as per the Pfizer requirements.Responsible for performing the SCNM (Site Compliance Network Member) activities at ZHOPL and create the PAC and PCF in the PDM systems.Responsible for the review and approval of submission package as per procedure REG-459.Review BoH Queries & response and compendial/scientific data changesResponsible for review and approval for NPL assessment and dossier handover to ZHOPLComplaint Management for Pfizer ProductTo coordinate and ensure that ZHOPL comply with the requirements for managing complaint.To review and approve the ZHOPL complaint investigation reports and upload investigation reports in the Pfizer electronic complaint database.Support for activities including co-ordination committee meeting and share the applicable information/ distribution details to site & & Pfizer market action leader function during market action and mock recall activity.Quality Management System (QMS) compliance functions: Responsible for Review and approval of Investigations (QARs) initiated at ZHOPL. To be part of SQRT and involve in the Investigations. Provide support for Supplier management. To provide Quality support for review of documents for new product launches and Tech transfers as needed Responsible for reviewing and approval of Process validation related performed at ZHOPL.Other: To support any additional and urgent activity in absence of primary responsible person as assigned by the Manager. Responsible to support with the AQRT /ESQRT process as and when required. To provide Quality support for new product launches and Tech transfer as and when neededPfizer Revolution Global SOPs management activities: Responsible for role of LPO for processes for Pfizer, Accountable for local process performance. Several LPOs could be assign to each L2 process, depending on local process requirements.Any other responsibilities assigned by the Manager.Qualification & ExperienceB. Pharm/ M. Pharm / M.Sc.10+ years of pharmaceutical industrial experience.Exceptional organizational and project management skillsDemonstrated strength in analytical skills and meticulous attention to detailA solid understanding of the regulatory and audit frameworks pertinent to biopharmaceutical operationsProficiency in taking decisive action based on quality and compliance metrics and trendsCapable of managing multiple complex projects with a strong sense of business acumenExcellent interpersonal effectiveness, coupled with superior written and verbal communication skills

ResponsibilitiesOverall responsibilities for quality assurance compliance at the Zydus Hospira Oncology Private Limited (ZHOPL) site and Pfizer Quality & ensure sustainable GMP compliance for Pfizer Products manufactured at ZHOPL site as per Quality agreement.Batch record review and release authorization compliance functions:Responsible for review and authorize the packed batch lot(s) for distribution in respective market from ZHOPL.To be part of SQRT as needed for any Batch related issue discussion.Regulatory impact assessment for all types of change related to Pfizer productsResponsible for Review and approval of Change controls at ZHOPL as per the Pfizer requirements.Responsible for performing the SCNM (Site Compliance Network Member) activities at ZHOPL and create the PAC and PCF in the PDM systems.Responsible for the review and approval of submission package as per procedure REG-459.Review BoH Queries & response and compendial/scientific data changesResponsible for review and approval for NPL assessment and dossier handover to ZHOPL  Qualification & ExperienceB. Pharm/ M. Pharm / M.Sc. with minimum 6+ years of experienceStrong understanding of Quality System functions, manufacturing and packaging processes, validations, batch documents , customer complaints, investigations, Training management, change controls, document Management.Ability to apply mathematical concepts, particularly statistics and probability, to Quality Engineering tasksExcellent technical writing, communication, and presentation skillsProficiency in Microsoft Office, Microsoft Project, and Statistical SoftwareExperience in preparing and participating in audits and inspections

ResponsibilitiesAdhere and comply with Organization Regulations and Administrative Policies.Adhere and comply with policies and procedure related to patient care, infection control, patient safety and accreditation standard.Care DeliveryDemonstrate clinical competence in all aspects of patient care.Evaluate the quality and appropriateness of care and assess the impact of nursing intervention as appropriate.Assessment and reassessment of pain and management of painEnsure compliance with all policy and procedure for medication management.Explain plan of care to patient and family.Document all patients records as per policies and standards.Educate patient and family as requiredEnsure the involvement of the patient, family and significant others in the patient's care.Quality ManagementMonitor clinical and other established performance indicators to ensure ongoing quality Improvement.Follow international patient safety goals.Report all near miss, sentinel events and any other incidents.Always maintain privacy and confidentiality of patient information and records.Comply with all quality standards as decided by organization for patient safety and quality of careTraining and DevelopmentParticipate and contribute in scheduled in service training programs like ACLS, BLS, PALS, NALS (If applicable), CNEs, conferences etc.,Functional Area ResponsibilityKnowledge on the blood drawing protocols and collection of reports.Alert the on-call physician/surgeon/ consultant in case of any deteriorating sings or abnormal lab results (Panic Value).Demonstrate knowledge on nursing care plan and its documentation.Ability to facilitate patient education.Knowledge on betadine/chlorhexidine (antiseptic)scrub bath prior to surgery.Administration of intra venous, intra muscular, intra dermal and subcutaneous injection.Perform steam inhalation, nebulisation and restrain policy.Assist / perform tracheostomy care and suctioning procedure.Ability to operate a Defibrillator.Ability to explain the discharge criteria as per policy.Management of blood and body fluids, HAZMAT spills.Handle central venous catheters and peripheral line.Knowledge on Anticoagulants and Urinary catheter care.Qualification & ExperienceEducation: Diploma / Bachelor’s degree in nursingRegistration: Valid registration in the state Nursing Council from where B.Sc. Nursing / GNM was completed.Experience: Freshers / candidates with 1 or 2 years of experience