Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, How Youll Spend Your Day In-depth knowledge of pharmaceutical quality and quality systems, with broad experience and exposure to best practices Knowledge of cGxP requirements, Quality related IT applications, and computer system validation and deployment Demonstrated experience with managing complex activities Must have international experience and experience working with large cross-functional teams Technical knowledge and expertise with Quality Management computer systems including Electronic Document Management Systems (EDMS)and Quality Management Systems (QMS) and processes (such as deviations, CAPA, laboratory investigations, complaints, trends, change control, document management, notification to health authorities, notification to Management, ), Skilled with Excel, Word, PowerPoint, MS Project and SharePoint Demonstrates resourcefulness and initiative and creates an appropriate level of urgency to meet objectives and deadlines Fluent in English Verbal and written communication excellence required Veeva Quality system knowledge a plus Your Experience And Qualifications Bachelors in Science is required and advanced degree preferred in science/regulatory/computer science/management field Minimum of 5-7 years in pharmaceutical or related industry is required Already Working @TEVA If you are a current Teva employee, please apply using the internal career site available on "Employee Central" By doing so, your application will be treated with priority You will also be able to see opportunities that are open exclusively to Teva employees Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well If you have trouble accessing your EC account, please contact your local HR/IT partner, Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,
Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, How Youll Spend Your Day Review and approval of method validation protocols and reports Review and approval of method transfer protocols and reports Review and approval of development study protocols and reports Review and approval of equipment/instrument calibration and maintenance records Review and approval of equipment/instrument validation/qualification documentation Review and approval of software validation/qualification documentation Review and approval of cleaning validation/verification documentation Review and approval of change controls related to SOPs, test methods, specification documents, forms, master batch records, and master packaging records Review and approval of test methods, specification documents, SOPs, master batch records, and master packaging records Review and approval of executed batch records and executed packaging records Review and approval of laboratory test data for raw materials, components, intermediates, and finished products Review and approval of stability data and stability summary reports Review and approval of environmental monitoring data/reports and associated documentation QA release of raw materials, components, and finished product batches Creation of new or revision of existing SOPs Support regulatory, external, and Teva global audits Support the Inspection Readiness Program Complete training assignments timely by the due date Assist with document number issuance for controlled documents Attend assigned meetings and provide updates as needed Assist with compiling site metrics, KPIs, and trend reporting Review of environmental monitoring charts and associated documentation Conduct corporate standards gap assessments Support the Vendor Approval Program (review of vendor documentation, QTAs, ) Train and maintain proficiency with computerized systems (Glorya, Veeva, Studium, IT systems, ) Perform other activities as assigned by the manager Your Experience And Qualifications Required undergraduate BA/BS degree in Life Sciences or related field A minimum of 3-5 Yrs of experience in Pharmaceutical QA GMP environment Equivalent combination of education and/or relevant work experience will be considered Already Working @TEVA If you are a current Teva employee, please apply using the internal career site available on "Employee Central" By doing so, your application will be treated with priority You will also be able to see opportunities that are open exclusively to Teva employees Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well If you have trouble accessing your EC account, please contact your local HR/IT partner, Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,
Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, How Youll Spend Your Day Preparation of data migration documents Perform source to target data mapping which requires detailed review of Analytical methods, Product Specifications, SOPs, monographs for conducting gap analysis Execute data migration design, configuration and validation activities Perform data configuration in LIMS software Laboratory information management system Proficiency in MS Excel is required, Must be detail oriented, fast learner, Good communication skills, Strong computer skills, preferred fluency in international language and ability to work effectively with international teams, Your Experience And Qualifications Sc Preferred: knowledge of LIMS software, Knowledge of SQL/Oracle/SAP Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,
Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, The opportunity Providing regulatory support for European and International Markets RA, How Youll Spend Your Day Completion of designated projects and tasks supporting European Market RA and International Market RA, according to internal Work Instructions, with guidance and direction by the manager and more senior colleagues, Maintaining related documentation and regulatory IT systems, in line with internal procedures, Timely task completion in line with Work Instructions, with accurate tracker updates and adherence to compliance standards, Communication with Teva units across Europe and International Markets, with 3rd Parties and with related Health Authorities, Fulfilling other allocated department duties and ad-hoc tasks as directed by senior regulatory affairs staff, Completion of trainings assigned in Teva internal learning management system within defined timeframes, Attending team meetings and providing regular updates on the assigned activities and tasks to the manager and/or to senior regulatory affairs staff, Maintaining and developing awareness of the current/pending regulatory legislation and guidelines, Qualification Your experience and qualifications Masters in Pharmacy or Masters in Science/Life Sciences College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts, Experience 2-3 years of experience in the Pharmaceutical Industry, ideally within Regulatory Affairs but R&D, Development or QA would be considered, Experience of regulatory documentation within Europe and/or International Markets, Knowledge Work experience involving core regulatory concepts and procedures, Ability to use existing internal procedures to solve routine or standard problems, Proficient in regulatory IT systems to support compliance and documentation processes, Working knowledge of Office-365 applications and Veeva Vault systems, Strong focus on Compliance and regulatory standards, Basic knowledge of project management principles and tools, Strong organizational skills to meet self, team and company goals, Ability to identify a problem or need for decision that exceeds the competence of the individual, French and/or German language proficiency will be an added advantage, Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience, Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws,