Responsibilities  Document Control Control issuance, revision, retrieval, and archival of QC documents — SOPs, STPs, specifications, logbooks, worksheets, MOA — per controlled document register. Maintain document cell registers — issuance, retrieval, archival, change history. Coordinate and ensure training of QC personnel on revised SOPs / specifications / MOA before effective dates.  Data Review & Compliance Review and verify analytical data from instruments such as HPLC, UV-Vis spectrophotometer, pH meter, KF auto-titrator, and balances — for completeness, signatures, calculations, and ALCOA+ compliance. Ensure testing is performed as per approved specifications and SOPs; flag any deviation in execution to supervisor. Verify SOP implementation and compliance across QC sections through periodic walkthroughs and document checks. Monitor GMP / GLP compliance in QC departments and follow up for corrective actions on observed gaps.  Investigation Support Support investigation of OOS, OOT, and laboratory incidents — gather raw data, chromatograms, instrument logs, and analyst notes for investigation files. Support continuous improvement initiatives in documentation and quality systems — paperless lab, e-logbook, LIMS adoption.Qualification & ExperineceQualification B.Sc / M.Sc / B.Pharm Experience 1 – 3 years; (OSD experience preferred)

ResponsibilitiesPeople Capability Development - Attend all local and regional meetings and training programs and acquire and apply knowledge as disseminated through such programs. New Hire Induction - Impart field induction training to new joiners monitor progress and give feedback to superiors. Make product presentation and assist area manager in PCM’s whenever required. Assist CSM in collection and summarizing of SLP sales leadership in plan formats. Attendance and participation at local/regional meeting Attendance and participation in training programs/seminar Financial Sales Target Achievement - Achieve monthly, quarterly and annual sales targets as assigned by CSM/RBM Inventory Management - Forwarding of breakage & expiry of products within limits of authority. Customer Acquisition Budget Management - Decide and effectively utilize financial investment for doctors within the ethical guidelines of the group. Target achieved % Growth Process Efficient Day Planning - Plan day’s work with clear objectives for each call, perform pre and post call analysis and visits chemists for feedback. Market Intelligence - Keep track of movement of company products vis-à-vis competitor’s products and give regular feedback to superiors. Assist the CSM to identify appropriate target doctors. Report adverse events to Pharmacovigilance. Effective utilization of SFE tools OPTIMA and SLP guidelines for process excellence.Qualification & ExpeirneceAny Graduate, preferably B.Sc or B.Pharma Relevant Work Experience Minimum Years Of Experience 2+ years of relevant experience Preferred industry experience Pharmaceuticals, Consumer Health Care

ResponsibilitiesReceipt & Issue of RM/PM and Dispatch of FG Plan and execute activities related to receipt & Issue of raw and packing materials and Dispatch of Finished Goods as per SOP with optimum utilization of resources. Co-ordinate Co-ordinate with Finance, Quality, Supply chain, and Procurement and execute necessary steps involved in receipts viz, making of GRNs, Sampling, PO amendments & PO release, etc. Co-ordinate with the Engineering Dept. for Equipment maintenance & other related activities for a smooth-running warehouse. Warehouse Maintenance Implement global warehousing standards and ensure compliance for GMP and HSE requirements. Initiate engineering-related work orders in HANA and ensure all get done on time to time. Carry out day-to-day maintenance of GMP documents/logbooks and formats as applicable. Statutory Compliances Ensure compliance with statutory audit requirements and physical stock verification. Material Planning Maintain the material receipt area to achieve continuous flow of incoming materials. Track the receipts as per the delivery schedule provided by the Supply chain. Coordinate with the supplier and approve the delivery schedule. GMP requirements Carry out day-to-day cleaning and housekeeping activities as per the SOP. Other Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations. Carry out destruction of old Warehouse records as per SOP and perform fixed assets mgmt. Ensure entire activities related to scrap management and maintain the required document/logbooks.Qualification & ExperineceGraduate in Science / Commerce /Pharmacy and Diploma in Materials Management preferable. Experience 2 to 5 Years of relevant experience in the pharmaceutical warehouse

Responsibilities Reporting to Zentiva Italy Quality & Compliance Manager, the Quality Operations Specialist will take lead responsibility for Product Quality Reviews (PQR) review completion for the cases in which Zentiva Portugal is marketing authorization holder (MAH). Responsible to meet the established schedule in completing the reviews of PQRs. For each evaluated PQR the Quality Operations Specialist will ensure that the traceability of the evaluation (report) is always available (document crated, approved/signed and properly archived) according to Zentiva Italy procedures. Responsible for flagging /escalating to the Zentiva Italy Quality & Compliance Manager any delays on time. Prepares trends analysis and KPI on PQR review process. Responsible for ensuring the maintenance of a up to date document for tracking of PQRs review operations and will support Zentiva Italy Quality & Compliance Manager in the preparation of periodic reporting of the PQRs review. The tracking document shall permit to Zentiva Italy to identify PQRs evaluated as “to be improved” or which are not meeting the requested quality standards. Responsible for calculating PQRs review KPIs on monthly basis. Responsible for the extraction and data compilation of analytical, manufacturing (including deviations, complaints, and change requests) from appropriate IT tools (Quality Forward, Share/DrugTrack, eDMS) and regulatory data (HA commitments, variations).Qualification & ExpeirenceGraduated / post-graduate in Pharmacy/Medicine or Chemistry/Biotechnology 3 to 6 years minimum experience in Quality or Regulatory Affairs Experience obtained in pharmaceutical manufacturing sites (+3 years). Knowledge of stability regulations and its application to the industry Skilled in the usage of IT tools (for example: Quality Forward, Share/DrugTrack, eDMS), SAP.

Responsibilities Reporting to Zentiva Italy Quality & Compliance Manager, the Quality Operations Specialist will take lead responsibility for Product Quality Reviews (PQR) review completion for the cases in which Zentiva Portugal is marketing authorization holder (MAH). Responsible to meet the established schedule in completing the reviews of PQRs. For each evaluated PQR the Quality Operations Specialist will ensure that the traceability of the evaluation (report) is always available (document crated, approved/signed and properly archived) according to Zentiva Italy procedures. Responsible for flagging /escalating to the Zentiva Italy Quality & Compliance Manager any delays on time. Prepares trends analysis and KPI on PQR review process. Responsible for ensuring the maintenance of a up to date document for tracking of PQRs review operations and will support Zentiva Italy Quality & Compliance Manager in the preparation of periodic reporting of the PQRs review. The tracking document shall permit to Zentiva Italy to identify PQRs evaluated as “to be improved” or which are not meeting the requested quality standards. Responsible for calculating PQRs review KPIs on monthly basis. Responsible for the extraction and data compilation of analytical, manufacturing (including deviations, complaints, and change requests) from appropriate IT tools (Quality Forward, Share/DrugTrack, eDMS) and regulatory data (HA commitments, variations).Qualification & ExpeirenceGraduated / post-graduate in Pharmacy/Medicine or Chemistry/Biotechnology 3 to 6 years minimum experience in Quality or Regulatory Affairs Experience obtained in pharmaceutical manufacturing sites (+3 years). Knowledge of stability regulations and its application to the industry Skilled in the usage of IT tools (for example: Quality Forward, Share/DrugTrack, eDMS), SAP.

Qualification & Experience Qualification: B.Sc / DMLT  Experience: Minimum 5 years  Gender: Female / Male 

Qualification & Experience    Qualification: DM / DNB    Experience: Minimum 2 years     Gender: Male / Female  

Qualification & ExperienceDepartment: BIOMEDICAL Designation: TRAINEE/APPRENTICE Qualification: DIPLOMA IN MEDICAL ELECTRONICS /B.TECH/B.E WITH RELEVANT EXP IN ANY REPUTED HOSPITAL

Qualification & ExperienceDepartment: OT Designation: PHARMACIST Qualification: B. PHARMA WITH RELEVANT EXP. OF 2-5 YRS. IN AN NABH HOSPITAL.

Qualification & Experience     Experience Required : 10 year       Qualification Required : Diploma/BSC Radiology