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 & 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

ResponsibilitiesTo conduct analysis of IP/FP/Stability/PV samples as allotted by the Group leader.Responsible for SAP activities and ROA preparation.Reviewing analytical records and raw data against Specification and STP.To ensure that the documentation done is online and error free.To ensure the correctness of the document before submitting it for the review of Group Leader.To ensure that only calibrated instruments/ equipment are used for analysis.To ensure that only valid reference standards are used for analysis.To ensure that the SOP / STP / reference standards are placed at their designated place after completion of the analysis.To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP.To ensure that the instruments / equipment are cleaned before & after analysis.To ensure that all Safety precautions and procedures are followed while conducting analysis.To report discrepancies in procedures / products to the group leader in time.To report Incidents / OOS / OOT in time to the Group leader.Any other responsibility assigned by Group Leader.Responsible for Lab Safety and follow the JSA.Ensure to use the proper PPE at workplace.To charge and withdrawal the stability sample as per interval. Stability study creation in SAP. Review the stability protocol.Ensuring timely completion of all the training assigned to selfQualification & ExperienceEducational qualification: B. Pharma/B.Sc/M.ScMinimum work experience: 2 to 5 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry

ResponsibilitiesResponsible for creating and managing project documentation, including change control documents, raw material specification, forms, protocols, reports, and other documents as assigned to support AR&D needs.Co-ordinate with QA for Change request for all project related activities.Co-ordinate with QA department to make specification/test methods effectiveness.Responsible for coordinating with the Purchasing Department as required for API related documents to support project needs. Responsible for assisting with the DMF review.Responsible for assisting in communication of general AR&D requirements to other departments.Responsible for supporting or assisting with the stability protocol preparation.Responsible to co-ordinate with regulatory department for any analytical documents requirements.Responsible for operating in accordance with the company’s Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.Other related responsibilities as assigned by R&D management.Major DutiesCreation of specifications for raw materials and supplies for R&D projects, and collection of documents required to support raw material assessmentsCreation of method validation/verification/transfer Protocols/reports, analytical test procedure, summaries, and other related documentation.Review and assess DMF to support API related analytical documents for development projectsWork with offsite groups to assist with the transfer of information to the Aveva site in support of R&D ProjectsAssist with the document review, preparation of project requirement, data compilation to support project requirements under supervisor guidance.Carry out change control process for any document preparation in trackwise system.Work with AR&D leads to satisfy project requirements. Qualification & ExperienceEducationBachelor’s degree (B.S.) in chemistry or related fieldMaster’s degree (M.S.)Knowledge, Skills and AbilitiesStrong organizational and communication skills, ability to work effectively with internal and external team members and work effectively as a team memberAbility to track project tasks and deliverablesStrong writing skills and ability to write clear, concise, documents of a technical natureGeneral knowledge of the pharmaceutical work environment, such as GMP and safety practicesComputer skills including MS Word, Excel, Powerpoint, and other relevant software programsAnalytical chemistry and common instrumentationGeneral understanding of HPLC, GC, Drug Release, UV, IR, Titration.ExperienceAt least eight (8) years experience in pharmaceutical laboratory (B.S)At least five (5) to seven (7) years experience (M.S.)

ResponsibilitiesResponsible for managing the hospital pharmacy, including dispensing medications, maintaining drug inventory, and ensuring accurate prescription fulfillment. Ensures compliance with regulatory standards and hospital policies, monitors drug storage conditions, and oversees proper labeling and documentation.Collaborates with doctors, nurses, and other medical staff to provide safe and effective medication management, counsel patients on proper drug use, and support clinical decisions for optimal patient care.Qualification & ExperienceExperience: 2-4 years Qualification: B.Pharm (Bachelor of Pharmacy), D. Pharm

ResponsibilitiesAssist in the execution of formulation and process technology transfers from R&D to manufacturing sites (in-house and CMO).Conduct scale-up and exhibit batches under supervision, ensuring proper documentation and parameter tracking.Support in the preparation and review of Batch Manufacturing Records (BMRs) and validation protocols/reports.Coordinate with R&D, QA, QC, Regulatory Affairs, and Manufacturing teams for effective knowledge transfer and execution.Participate in process investigations, troubleshooting, and deviation handling during trial and validation batches.Assist in equipment selection and capacity assessment based on product-specific requirements.Ensure document readiness for regulatory submissions, respond to technical queries, and support audit preparation.Support internal and external/vendor audits by providing required documentation and technical inputs.Contribute to continuous improvement initiatives and support knowledge-sharing activities within the MSTG team.Prepare data summaries, technical reports, and presentations as per project or management requirements.Maintain accurate records, follow applicable SOPs, and ensure strict GMP compliance in all operations. Qualification & ExperienceB.Pharm / M.Pharm in Pharmaceutics or Pharmaceutical Technology.2–5 years of experience in formulation development, MS&T, or technology transfer.Exposure to solid orals, liquids, or softgel capsule dosage forms.Understanding of scale-up principles, equipment functionality, and validation practices.Familiar with regulatory expectations (USFDA, EU, etc.) and cGMP standards.Good communication, documentation, and teamwork skills.Willingness to travel to manufacturing sites as per project requirements.

ResponsibilitiesResponsible review of exhibit batch manufacturing records and exhibit batch packing records before execution of the batch.Responsible for review of process validation protocol and reports, hold time protocol and reports.Responsible for review of executed media fill records for regulatory submissions.Responsible for review and submission of executed exhibit batch manufacturing records and batch packing records.Responsible for review and submission of process validation reports and hold time reports.Responsible for review and submission of intended batch manufacturing records.Responsible for review and submission of product related equipment’s qualification documents.Responsible for review of QMS documents like Change control, deviation and CAPA. Qualification & ExperienceM.Pharmacy or Any Postgraduate.

ResponsibilitiesResponsible for review of process validation protocol and reports, hold time protocol and reports.Responsible for review of executed media fill records for regulatory submissions.Responsible for review and submission of executed exhibit batch manufacturing records and batch packing records.Responsible for review and submission of process validation reports and hold time reports.Responsible for review and submission of intended batch manufacturing records.Responsible for review and submission of product related equipment’s qualification documents.Responsible for review of QMS documents like Change control, deviation and CAPA. Qualification & ExperienceM. Pharmacy or Any Postgraduate.

ResponsibilitiesAssist physicians during patient consultations and clinical proceduresReview patient medical history, medications, and treatment plansProvide medication counseling and drug information to patientsMonitor patient progress and report updates to physiciansCoordinate with nursing, laboratory, and pharmacy departmentsMaintain accurate patient records and clinical documentationSupport prescription review and medication safety practicesAssist in patient education regarding treatment and medication adherenceParticipate in ward rounds and clinical case discussionsEnsure compliance with hospital protocols and healthcare regulationsQualification & ExperienceDoctor of Pharmacy (Pharm D) qualification from a recognized institution0–3 years of experience in hospital or clinical practice preferredStrong knowledge of pharmacology and clinical practicesGood communication and interpersonal skillsAbility to work collaboratiaxvely in a healthcare teamBasic computer knowledge and medical documentation skillsKnowledge of hospital information systems is an added advantage

ResponsibilitiesResponsible for managing the hospital pharmacy, including dispensing medications, maintaining drug inventory, and ensuring accurate prescription fulfillment. Ensures compliance with regulatory standards and hospital policies, monitors drug storage conditions, and oversees proper labeling and documentation. Collaborates with doctors, nurses, and other medical staff to provide safe and effective medication management, counsel patients on proper drug use, and support clinical decisions for optimal patient care.Qualification & ExpeirenceB.Pharm (Bachelor of Pharmacy), D. Pharm2-4 years experience