Start a career with purpose.
At GSK, we unite science, technology, and talent to get ahead of disease together. Our goal is to improve the lives of billions across the world. By bringing together outstanding people in an inclusive environment, we can make an impact on a global scale.
oferujemy
- Opportunity to participate in training and improve skills,
- Opportunities for development within the company structure,
- Work culture based on respect, honesty and focus on consumer needs,
- RandstadPlus – benefits system (sports card, private medical care, discounts on online shopping),
- Possibility of breaks in the internship due to holiday plans,
- Possibility of employment by GSK
zadania
Submissions Delivery Specialist, Publishing will be responsible for producing
submissions delivered to Regulatory Authorities worldwide in support of the
entire product lifecycle, ensuring that all submissions are produced as specified by GSK delivery teams (time and content) and are compliant with appropriate Regulator’s electronic submission standards.
Responsibilities:
• Assemble, link and publish submission packages that meet Regulatory
...
Authority technical standards and GSK requirements and schedules
• Advising and assisting authors with the preparation of submission content
and use of GSK document management systems and procedures
• Check compliance of others’ work with requirements and standards
• Maintaining knowledge of relevant Regulatory Authority rules and GSK
standards associated with submission format
• Interpreting and correcting technical validation errors, identifying and
resolving issues with source documents, working with authors and requestors as
necessary to rectify any problems that prevent completion of the publishing job
• Participate in implementation of publishing working practices and
procedures aimed at simplifying processes and increasing quality
• Regular interactions with publishing staff globallyoczekujemy
Basic qualifications:
• Bachelor’s or Master's degree in scientific or technical field
• Previous experience (in regulatory affairs, pharmaceutical industry, life
sciences research)
• Fluent in Polish and English (both spoken and written)
• Technical Proficiency – Strong knowledge of common computer
applications (e.g., MS Office, Adobe Reader) and, ideally, experience with
complex IT tools in large organizational settings
• Ability to quickly adopt and navigate to new tools and technologies
• Analytical thinker with problem solving skills
• Paying attention to detail and ability to follow detailed procedures
consistently
• Strong interpersonal, customer service skills with experience working in a
complex, global, cross functional organization
Preferred qualifications:
• Familiarity with Veeva Vault
• Data Analytics Proficiency in MS Excel
• Process Improvement Mindset – Strong critical thinking skills to enhance
efficiency
Agencja zatrudnienia – nr wpisu 47
ta oferta pracy przeznaczona jest dla osób powyżej 18 roku życia
