ResponsibilitiesTo provide nursing care as per guidelines of the consultant and departmental standardsExperienceWork Experience7 - 12 YearsQualificationBSC/ GNM/PBBSC/ MSc

ResponsibilitiesObtain and document patient assessment incorporating all available data and information. Plan and document a nursing care plan using the nursing process and set priorities of care. Deliver care using the nursing process; delegate and supervise care delivered by junior staff nurses. Evaluate each shift's nursing interventions and document; revise care plans as required. Participate in Nursing Quality Assurance programs. Identify unsafe care practices and contribute to corrective action. Take over from previous shift nurse and check bedside checklist items. Render nursing care to assigned group of patients (bed making, sponging, mouth care, back care, etc.). Observe and report symptoms and condition of patients to the doctor as and when necessary. Record TPR, BP; administer medications; note reactions; set up treatment trays.ExperienceWork Experience1–5 Years

ResponsibilitiesCompleting the joining formalities like arranging shoes, uniforms, lockers etc for the new recruits in the department Vaccination of newly joined candidates in Pediatric OPD Distribution of the permanent IDs of newly joined candidates. Preparation of Induction Schedule Booking of the classrooms on 7th Floor Coordination with Speakers (Lecturers) Execution of the Programme Designing of Training Module e.g. Lecture Method, Discussion, Practical Session, Equipment orientation, Hospital orientation etc. Post Induction Test on topics covered in the Induction Programme Analysis of evaluation of the test results. Feedback session from the participants regarding the content of the Programme, speakers, need for improvement in any areas, suggestions etc. Inform the unit in charges of the staff about the improvement required.Experience5 - 12 YearsQualificationBSC/ GNM/PBBSC/ MSc

ResponsibilitiesQuality management of deviation and complaint records and their related CAPAs Assessment and management of change controls Edition of QA Agreements with Zentiva third parties and subcontractors Collection and evaluation of PQRs and stability data Compliance evaluation of Third Parties and products Maintenance of product database Collection and review of CoA/CoC QA support of product launches and transfers GMP, GDP, MDR, HACCP, Food Supplements and Cosmetics regulations and legislations Auditing Prepare audit and audit plans Conduct and participate to external audits Evaluation of audit reports Participate to internal audits and inspections KPI monitoring and reportingQualification & ExpeirenceUniversity degree in Pharmacy, Chemistry, Biology, or relevant Life Science Minimum of 5 years in a similar role or equivalent experiences in a GMP related environment Thorough knowledge of GMP requirements as well as knowledge of ICH and pharmaceutical regulatory requirements Management of subcontractors is an advantage Proven track record of project management skills Strong communication skills and negotiation strength

ResponsibilitiesPerforming and organizing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals. Performing and organizing analysis of market complaints, Stability, process validation, Cleaning Validation samples of Pharmaceuticals. Good Laboratory Practice Performing and organizing calibration / maintenance of lab. Equipment and assisting for the qualification of laboratory equipment. Reviewing pharmacopeias for specification preparation. Preparing SOPs, Formats, Specification, Analytical Test Record and other documents. Managing reference standards, working standards, Laboratory chemicals & reagents. Managing instrument laboratory with reference to spares, maintenance etc. Managing Control Samples and related record. Approval / Rejection of Raw Materials, Packaging materials, in process materials, Bulk Finished products and bulk medical device. Investigating out of specification results, retesting and review the analysis records. Maintaining & reviewing laboratory raw data and log book related to testing activity. Responsible for reviewing the chromatographic data.Qualification & ExpeirencePost Graduate in Science (Organic or Analytical Chemistry) or B.Pharm/M.Pharm 5-7 years in chemical & instrumental testing laboratory with exposure to GMP, GLP

ResponsibilitiesImplementation of Zentiva Global Quality & Regulatory policies & guidelines, review and approval of GxP Documents e.g. Quality Manual, SOPs, Process Validation reports, Master Batch Records, Finished Product specifications, Master Documents, etc. Submission to regulatory authorities associated with various regulatory requirements, authoring / or coordinating RA activities for new registrations / licenses, post approval changes, renewals, GMP Certification applications, annual reports and line extensions to meet requirements.Coordinating and contributing to responses to Agency queries and performing quality review of regulatory submissions.Coordination for cGMP Training activity including training of identified people.Review and approval of Artwork / Labelling.Qualification & ExpeirencePostgraduate in Pharmacy Experience 10 years in Pharma industry with awareness of Quality management systems, Analytical testing, Method Development/Validation, Manufacturing activities, Process validation, Qualification, Regulatory requirements.

ResponsibilitiesEnvironment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualification & ExperienceQualification: M.Sc (Microbiology) / B.Pharm Experience: 6-9years EM monitoring in aseptic process area including Grade A,B,C and D

ResponsibilitiesEnvironment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualification & ExperienceQualification: M.Sc (Microbiology) / B.Pharm Experience: 3-4 years EM monitoring in aseptic process area including Grade A,B,C and D

ResponsibilitiesConduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental conditions Communicate findings and recommendations to stakeholders and management Participate in environmental remediation and restoration projects Ensure compliance with environmental regulations and standards Growth promotion test, Media preparation, Autoclave operation, Cleaning and disinfectant preparation. Calibration of instruments.Qualification & ExperienceQualification: M.Sc (Microbiology) Experience: 2-7 years Person having work experience in GLP section in Microbiology section.

Qualification & ExperienceMBBS, MD/DNB, DM Experience: Minimum 3 years and above post DM