Senior Regulatory Specialist - Global Labelling
GlaxoSmithKline plc
Poznan Grunwaldzka
5 d. temu

GSK currently has opportunities in its Global Regulatory Affairs (GRA) - Labelling department, within research and development.

These roles are perfectly suited for enthusiastic regulatory professionals with experience or an interest in managing patient and prescriber information and who would like to pursue a career in a global pharmaceutical company.

Our Labelling team supports a product during development and throughout its lifecycle, and we are the coordinating authors of Company Core Datasheets for GSK pharmaceutical products.

This position includes working with colleagues in Local Operating Companies worldwide in order to deliver in a timely manner high quality documents required for local submissions.

Ensuring that all appropriate local requirements aspects are in place, to maintain clarity and quality of Local Labelling Submissions.

You may liaise with colleagues in clinical, safety and other regulatory functions to ensure that the Prescribing Information, Patient Leaflets and Packaging Components accurately state the Company's medical and scientific position regarding the safe and effective use of a GSK product.

Your Responsibilities :

  • Providing Local Operating Companies with required documents for national labelling submissions
  • Participating in the development of the Company Core Datasheet (Global Product Information) for new medicines or product line extensions.
  • Maintenance of country / regional labelling in compliance with GlaxoSmithKline labelling processes and external requirements for local markets e.
  • g. Europe (for Centralized, Mutual Recognition and Decentralized procedure submissions), US and International countries.

  • Managing core and local prescribing / patient information throughout the product lifecycle.
  • Working with colleagues in GSK Local Operating Companies in markets worldwide to ensure the company core datasheet is accurately reflected in local prescribing / patient information.
  • Basic requirements :

  • Relevant experience (in pharmaceutical industry, life sciences research, regulatory or medical affairs, clinical research, pharmacovigilance or alternatively therapeutic area experience from research).
  • Successfully performed within a regulated or quality-critical environment (such as pharmaceutical industry research or regulatory).
  • Attention to detail, excellent organization and time management skills.
  • Excellent written and verbal communication skills and ability to present information in a clear and concise manner.
  • Ability to think flexibly to meet constantly shifting priorities and timelines and to independently provide solutions to issues.
  • Understanding of the pharmaceutical industry, drug development environment, and regulatory processes.
  • Understanding of product information / labelling (e.g. direct or indirect management of labelling documents and submissions).
  • Experience with PIL and SPC procedures will be a strong asset.
  • Fluent communication in Polish and English.
  • We offer :

  • We offer the opportunity to gain experience in well-known company, to cooperate with international environment where you can have an access to cutting-
  • edge technology and work in friendly atmosphere.

  • We provide an attractive remuneration package and benefits (e.g. private medical healthcare, life insurance, sports card, pension plan, flexible working hours, home office), as well as the prospects of a comprehensive professional development.
  • GSK corporate culture is based on our values : patient focus, integrity, respect and transparency.
  • If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK HR 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 / Agencies

    GSK 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.

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