OverviewSite Name: Italy - Siena; Belgium - Wavre; Poznan Grunwaldzka; UK – London – New Oxford Street.Posted Date: Oct 23 2025Job DescriptionWe 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 Life at GSK page.Locations: Siena, Italy / GSK HQ, UK / Wavre, Belgium / Poznan, PolandScopeResponsible for the CMC regulatory activities in the late phase development and/or commercial lifecycle management of GSK products.Responsibilities:Responsible for the global CMC regulatory activities for assigned projects and responds readily to changing events and priorities.Responsible for CMC strategy development, with managerial support, for CMC submission documents to support marketed product lifecycle management activities in accordance with applicable regulatory and scientific standards.Interpret regulations, guidelines, procedures and policies relating to manufacture and control of medicinal products to advise teams and expedite submissions.Ensure all appropriate CMC regulatory aspects for product release are in place to ensure continuity of market supply and that lifecycle submissions meet regional requirements.Work in cross-functional matrix project teams with regulatory, development, quality and manufacturing to define proper regulatory CMC filing strategy.Maintain high quality standards and pursue continuous improvement and innovation in response to evolving regulatory environments.Share regulatory compliance best practices within CMC Regulatory teams and other impacted functions.Engage in CMC Subject Matter Expert activities internally to increase compliance, harmonisation and efficiency.Deliver CMC regulatory strategy to support major inspections with managerial support.Why you?Basic Qualifications:Bachelor or Master Degree in life sciences or related scientific discipline.Regulatory Affairs Certification (RAPS).CMC regulatory affairs or product development experience with involvement in regulatory submission preparation in late phase development and/or marketed product lifecycle submissions.Knowledge of drug development, manufacturing processes and supply chain; may have a specialized area of expertise.Knowledge of worldwide CMC regulatory requirements and a track record of delivering compliant dossiers, particularly for marketed products.Fluent English, written and spoken.Preferred QualificationsNote: The following skills are preferred but not required. If not available, please still apply.Time management and ability to plan, prioritize and coordinate multiple tasks to meet deadlines.Growth in global regulatory affairs and understanding evolving trends and policies across regulatory functions.Experience influencing and negotiating with company personnel and regulatory agencies.Strong interpersonal, presentation and communication skills with internal networks.Potentially identified as CMC Regulatory expert in a specific subject area.Proactive in suggesting process improvements; ability to develop and implement regulatory strategies and assess impact on project strategy.Experience handling global CMC issues through change and improvement.Developing experience in major post-approval filing activities.What we offerPermanent contract in an inclusive environmentSmart Working up to 50% for eligible rolesPerformance RewardFlexible BenefitsCompany Healthcare PlanIntegrative pension fundEmployee Assistance ProgrammePrevention services and vaccination clinicTax assistanceLocal nursery agreementPostal service, laundry, shoe repair and tailoringOn Site GymOn Site canteens and coffee cornersFree company bikes and shuttleClosing DateClosing Date for Applications – 5th of NovemberRelocation note: Please note relocation support cannot be provided; therefore, only candidates already based in the indicated country can be considered.Application InstructionsPlease take a copy of the Job Description, as it will not be available post closure of the advert. When applying, describe how you meet the competencies for this role in your cover letter or CV. The information provided will be used to assess your application.#LI-HybridNote: Some standard company information and external links were removed to comply with formatting guidelines.
#J-18808-Ljbffr