Are you looking for a regulatory affairs role that will enhance your documentation knowledge and allow you to help shape systems strategy?  If so, this Regulatory Affairs Operations role could be an exciting opportunity to explore.

Regulatory Specialist supports operational activities related to maintenance of marketing authorisations (MAs) across assigned markets and/or submission types in European Partnership Markets, working in close collaboration with country leads, as well as global regulatory teams/centers and local 3rd party service providers, if applicable/directed.

This role will provide YOU the opportunity to lead key activities to progress YOUR career.  These responsibilities include some of the following:

• Supporting country leads in activities related to maintenance of marketing authorizations (MAs) for assigned markets and/or submission types across pharma and vaccines portfolio

• Providing inputs and support to planning and tracking of regulatory activities for defined markets/submission types

• Managing routine operational steps within Regulatory Information Management (RIM) systems related to the local activities within end-to-end regulatory processes, including data assessments

• Supporting country leads with operational activities related to responses to regulatory questions and commitments; providing direct inputs depending on complexity and scope

• Collaborating with global regulatory centers (GRC), if required, to support effective management of product registration documents and agency correspondence in RIM systems

• Collaborating with global regulatory teams/centers to ensure compliance of regulatory documentation for different submission types with countries’ requirements

• Supporting country leads with coordination of regulatory activities with external 3rd Party regulatory service providers

• May be supporting country leads with activities related to timely trigger of products artwork updates

• Building and maintaining effective relationships with internal and external stakeholders

Why you?

Qualifications:

• Master’s/ Bachelor's degree (in scientific discipline (life sciences / pharmacy / professions aligned to medicine)

• Approximately 2 years of relevant experience in regulatory affairs and pharmaceutical industry

• Understanding of the pharmaceutical industry, and regulatory processes related to license maintenance

• Awareness of the policies and regulatory climate in Europe.

• Experience gained across various submission types (CMC and/or labelling) is preferable.

• Experience of working effectively in a matrix organization and/or international environment is preferable

• Fluent English language skills (speaking and writing)

• Experience with Labelling will be an asset

Why GSK?

What we offer:

• Career with purpose - whatever it is you’re doing, you’ll be sharing our mission to improve the quality of human life, by enabling people to do more, feel better and live longer

• Non-wage benefits (medical care, life insurance, pension scheme, sports card, recreation allowance, social fund, preventive healthcare services)

• Hybrid working model

• Career at one of the leading global healthcare companies

• Supportive & friendly working environment

• Corporate culture, based on being Ambitious for patients, Accountable for Impact and Doing the right thing, which powers our purpose, drives delivery of our strategy and helps make GSK a place where people can thrive

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Inclusion and diversity at GSK are key for our success. Here, you will thrive through bringing your unique experiences to both our company and the recruitment process. We want you to be you, feel good and keep growing your career.
GSK is an Equal Opportunity and Affirmative Action Employer. Applicants will travel through a transparent recruitment journey that adheres to all required employment standards and regulations. Beyond this, we commit to our values of integrity and respect towards every applicant.
We want to hear from you and support with any adjustments that you may require during the recruitment process. Please get in touch with our Recruitment Team ([email protected]) to further discuss this today.
We will request equal opportunities information from you and whilst disclosure is optional, we encourage you to be open, enabling us to monitor the inclusivity of our recruitment practices for the benefit of everyone. Your data will remain confidential, is never shared with our Hiring Managers and never affects the status of your application. *Local restrictions/legal requirements

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Why GSK?

Uniting science, technology and talent to get ahead of disease together.

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 organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

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 place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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.

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