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Regulatory Affairs Specialist

Regulatory Affairs Specialist
Empresa:

Glaxosmithkline



Função de trabalho:

Jurídico

Detalhes da Vaga

Site Name: LisbonPosted Date: Apr 9 2024We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSKJob PurposeObtaining marketing authorization approval and lifecycle management of products under its responsibility ensuring compliance with national/European legislation and internal SOPs/WoWsBack-up of local responsible for Artwork Management using Harmony & GLAMS systems: coordination of packaging materials, new product introduction (NPI, new presentation pack, new indication, new line extension) with the objective of assuring its continuos update, in compliance with the legislation and local procedures to maintain continuous supply.In this role, you will...Management of submission and follow-up of MAA requests, variations, renewals and MAH transfers until regulatory approval with National Authority for products under its responsibilityShare with local stakeholders' regulatory timelines on new products/line extensions in pipeline/product already approved, including relevant regulatory information regarding competitors and submission and management of abbreviated risk minimization measures with local Authority (when applicable)Support and coordination with local Co-Promoted 3rd party ensuring regulatory compliance and ensure updating of Regulatory Information Management System/KPI input when required.Back-up of local responsible for Artwork Management: responsible for the preparation and sending of the due documentation for the NPI, New Packs, Line Extensions, updates of current MA for the creation of new packaging components for marketed products. Coordination of the new artwork proofs between Regional Service Center or local Agency and the local RA team and Supply Chain, to comply with the regulatory requirements (local and GSK) for their implementationReview and approval of packaging materials to confirm they are in compliance with the current legislation/internal SOPs & WoWsManagement of payment of regulatory fees to National Authority. Management and coordination of CPP requests and Participation on the training plan for new RA TraineesWhy you?Basic RequirementsWe are looking for professionals with these required skills to achieve our goals:Minimum Level of Education: Degree/Master's degreeArea of Specialisation: Pharmaceutical SciencesExperience in Regulatory Affairs AreaHigh level of EnglishPreferred Requirements:Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:Ability to work in a teamSense of responsibilityGood knowledge of information technology as userJob Posting End Date: 22/04/2024Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.Why Us?GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.#J-18808-Ljbffr


Fonte: Whatjobs_Ppc

Função de trabalho:

Requisitos

Regulatory Affairs Specialist
Empresa:

Glaxosmithkline



Função de trabalho:

Jurídico

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