Job Description 105,000 people reimagining medicine for more than 750 million people globally. That is also the number of people you may impact as our new internal consultant Your responsibilities include but not limited to: - As the Team Lead – Cross Border, Patient Group & Head Quarter Transparency Reporting, you will have to - Lead an operational team to contribute to the planning and execution of country specific service adoption plans including a report production planning, process adoption, quality reviews, communications and reporting readiness - Develop specialist knowledge on all reportable EFPIA Cross Border spend data and work with compliance, business and divisional leads to provide consultative support to local affiliates - Contribute to the design and implementation of EFPIA Cross Border processes and practices and resolve any gaps with existing or new / improved business processes including working with the Pharma AG and US transparency teams to improve the end-to-end p

Expected QualificationB E B Tech Instrumentation Electronics or Diploma in Instrumentation Electronics from reputed university collegeExpected Work Experience Minimum 5 Years to 10 Years of relevant experience in with Large scale organization Preferred industry Pharmaceutical API Formulation Chemical and AgrochemicalExpected CompetenciesInstrumentationConstruction Management Familiar Standards CGMP USFDA ASME ANSI SMACNA ISO Key Responsibilities Erection Installation and commissioning Of Instrument Systems Checking of Instrument Installation as Per P I Drawing Calibration of instruments Like PT FT TT DPT Control Valves etc Commissioning and Erection Experience in Pharmacy plants utility plants boiler systems Handson Experience Loop Checking and Functional Testing of All Instruments Line Up and Error Correction the Actuators Control Valves and Field Instruments Commissioning assistance of SWAS Panel SCADA system Servicing and Calibration of Pneumatic and Electronics Positioned and Contr

Job Description 28,000 associates of more than 100 nationalities deliver high quality and affordable medicine on time, every time, safely and efficiently. Job Purpose: Provide Quality Service in compliance with cGMP regulatory requirements and the Novartis Pharma Quality Manual and Policies by implementing processes, systems and tools that realize the Quality Operations services across Novartis divisions. Your responsibilities include, but not limited to - Perform and deliver Quality Operations services in support of product quality compliance and regulatory workflows. - Hold accounts in workflow applications (like SAP, Dragon, SUBWAY, TEDI etc.) to ensure appropriate execution of service deliverables. - Escalate service related GxP and non-GxP issues and ensure timely investigation and compliance with local and global operating procedures. - Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed product quality standards and service level

Quality Auditor GLP Quality Assurance Quality Auditor GLP Job Title Quality Auditor GLP Desired Qualification Experience A minimum of postgraduate in Science Pharmacy with at least two years experience Job Profile Should be working as GLP auditor in a preclinical CRO inhouse facility of a pharmaceutical Chemical Agrochemical Should have a though understanding of principles of OECD USFDA EPA GLP and requirements of NGCMA The candidate should have thorough understanding of OECD testing guidelines followed in testing of chemicals Proficiency in spoken and writing English with good communication skills would be desirable Location VLS Division Support Services Department Quality Assurance Show moreShow less The original job offer can be found in Kit Job: www.kitjob.in/job/17786915/ihj78-quality-auditor-bibinagar/

Quality Auditor GLP Quality Assurance Quality Auditor GLP Job Title Quality Auditor GLP Desired Qualification Experience A minimum of postgraduate in Science Pharmacy with at least two years experience Job Profile Should be working as GLP auditor in a preclinical CRO inhouse facility of a pharmaceutical Chemical Agrochemical Should have a though understanding of principles of OECD USFDA EPA GLP and requirements of NGCMA The candidate should have thorough understanding of OECD testing guidelines followed in testing of chemicals Proficiency in spoken and writing English with good communication skills would be desirable Location VLS Division Support Services Department Quality Assurance Show moreShow less The original job offer can be found in Kit Job: www.kitjob.in/job/17786915/ihj78-quality-auditor-bibinagar/

Quality Auditor GLP Quality Assurance Quality Auditor GLP Job Title Quality Auditor GLP Desired Qualification Experience A minimum of postgraduate in Science Pharmacy with at least two years experience Job Profile Should be working as GLP auditor in a preclinical CRO inhouse facility of a pharmaceutical Chemical Agrochemical Should have a though understanding of principles of OECD USFDA EPA GLP and requirements of NGCMA The candidate should have thorough understanding of OECD testing guidelines followed in testing of chemicals Proficiency in spoken and writing English with good communication skills would be desirable Location VLS Division Support Services Department Quality Assurance Show moreShow less The original job offer can be found in Kit Job: www.kitjob.in/job/17786915/ihj78-quality-auditor-bibinagar/

Quality Auditor GLP Quality Assurance Quality Auditor GLP Job Title Quality Auditor GLP Desired Qualification Experience A minimum of postgraduate in Science Pharmacy with at least two years experience Job Profile Should be working as GLP auditor in a preclinical CRO inhouse facility of a pharmaceutical Chemical Agrochemical Should have a though understanding of principles of OECD USFDA EPA GLP and requirements of NGCMA The candidate should have thorough understanding of OECD testing guidelines followed in testing of chemicals Proficiency in spoken and writing English with good communication skills would be desirable Location VLS Division Support Services Department Quality Assurance Show moreShow less The original job offer can be found in Kit Job: www.kitjob.in/job/17786915/ihj78-quality-auditor-bibinagar/

Job Description 28,000 associates of more than 100 nationalities deliver high quality and affordable medicine on time, every time, safely and efficiently. Job Purpose: Provide Quality Service in compliance with cGMP regulatory requirements and the Novartis Pharma Quality Manual and Policies by implementing processes, systems and tools that realize the Quality Operations services across Novartis divisions. Your responsibilities include, but not limited to - Perform and deliver Quality Operations services in support of product quality compliance and regulatory workflows. - Hold accounts in workflow applications (like SAP, Dragon, SUBWAY, TEDI etc.) to ensure appropriate execution of service deliverables. - Escalate service related GxP and non-GxP issues and ensure timely investigation and compliance with local and global operating procedures. - Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed product quality standards and service level

Job Description 20 years of untapped data waiting to be explored. The digital revolution is changing everything, especially in pharmaceuticals, and Novartis has embraced a results-oriented strategy to drive a company-wide digital transformation. With this mission, we are setting up a Data as a Service team at Novartis Hyderabad, which would work with the Chief Digital Office, Novartis Business units and industry leading technology partners, to drive the execution of Novartis’ data strategy, turning its rich data resources into real strategic assets to drive meaningful insights across the organization. This ambition is one of key pillars in the broader digital transformation happening at Novartis to be a ‘medicines and data science company. Major Accountabilities/Responsibilities Your responsibilities include, but not limited to: - Enables onboarding of data assets to the FAIRification process by working with relevant stakeholder, systems to identify data and metadata - Help creation of

Lead a team of 2-3 technicians provide management and scientific support to train lab members and promote their career development Develop efficient interactions with stakeholders within and outside in-vivo team, Provide scientific expertise, establish and monitor external scientific collaborations, monitor & provide critical assessment of SHIPL products. Planning and co-ordination for testing of in-process, in-vivo, final blend and finished product of Shan5 and Shan 6 vaccines. Review of validation protocols and co-ordination in v alidation studies. and qualification of in-vivo In-house Reference Standards. Planning and co-ordination for testing of stability samples asper TAT timeline. Handling of QMS activities related to in-vivo tests and its timely closure. Ensuring animal uses as per approved IAEC protocols and its update. Awareness about IP, BP, US pharmacopeias and WHO TRS guidelines. Actively participant for 3Rs programme as defined by pharmacopeias. Effectively work and commu

Job Description 365 days a year, our global manufacturing and supply network works to ensure our patients have the treatments they need to live longer, healthier lives. Position Purpose: Use the GxP experience and the well-established knowledge of Quality Management System and the relevant International Legislation to come up to the operational business in compliance with cGMP regulatory requirements and the company Pharma Quality Manual and Policies. Support PLS delivery by implementing processes, systems and tools that realize the Quality Operations services across Novartis divisions. Support the successful implementation of the NBS vision and strategy and the Novartis Quality strategy within PLS-M&SO; organization. Your responsibilities: Your responsibilities include, but are not limited to: - Perform Product Quality service operations like technical complaints, technical deviations, product change requests, product release, supplier qualification, product quality review, artworks

Job Description 105,000 people reimagining medicine for more than 750 million people globally. A global role leading all aspects of design, development and implementation of Pharma commercial and medical services and business solutions for Novartis’ internal shared services organization called NBS CONEXTS. The Senior Global Program Lead is responsible for the development of the services, solutions and target operating models within NBS CONEXTS. This encompasses the both evolution of existing and identification of new services and business solutions. The role leads the shaping and deployment of all support elements required to deliver and operationalize the services, such as identification of resource requirements, development of the business case, location strategy, process definition and management, customer engagement and stakeholder management. The role would suit someone who has developed advisory business services or someone who has delivered medical, commercial or other business

Novartis India \- Bibinagar, Telangana \- handling of chemicals, potentially dangerous materials and equipment. Broad theoretical and scientific knowledge in the relevant area \(e.g. manufacturing, analytical, pharmaceutical\) \- Skilled scientist with expertise on quantification of impurities and impurity profiling of unknown impurities in the drug product by using LCMS/LCMS/MS and GCMS, HRMS and the data interpretation.\-Experience on dealing OOS/OOE and deviations involving above mentioned analytical techniques \- Proficient with laboratory.

Job Description 105,000 people reimagining medicine for more than 750 million people globally. A global role leading all aspects of design, development and implementation of Pharma commercial and medical services and business solutions for Novartis’ internal shared services organization called NBS CONEXTS. The Senior Global Program Lead is responsible for the development of the services, solutions and target operating models within NBS CONEXTS. This encompasses the both evolution of existing and identification of new services and business solutions. The role leads the shaping and deployment of all support elements required to deliver and operationalize the services, such as identification of resource requirements, development of the business case, location strategy, process definition and management, customer engagement and stakeholder management. The role would suit someone who has developed advisory business services or someone who has delivered medical, commercial or other business

Job Description Ensure preparation, validation, dispatch and submission of compliant and high quality initial, 2nd wave and maintenance Regulatory filings according to submission plans. Update respective Regulatory systems for Registration Management, Publishing and Document Management. Support the Global Regulatory teams during the product development phase and provide input as appropriate. Follow Regulatory procedures and timelines Minimum Requirements University or College Degree in any field or life science with relevant industry experience or comparable degree Good communication in English (oral and written). - At a minimum 2 years’ experience in the Pharmaceutical area, specifically in Regulatory Operations - Experience in the Regulatory submission publishing, area is preferred - Knowledge of Regulatory guidelines for the areas mentioned above - Organizational awareness and experience working cross-functionally and in global teams is a plus - Ability to work under pressure, demon

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