Base: 95.000 pln to 152.000 pln annually; bonus/eq...
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Coordination of translation activities
Quality check of labeling documents
Compliance maintenance of labeling documents
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Johnson & Johnson is seeking an RA Professional Labeling for a one-year contract in Warsaw, Poland. The role involves coordinating translation activities of labeling documents and ensuring compliance with regulations while working within a collaborative, multicultural environment.
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Job Summary
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases with smarter and less invasive treatments.
The RA Professional Labeling EMEA role involves coordinating translation activities, quality checks, and maintaining compliance of labeling documents in cooperation with multiple stakeholders.
The company provides an inclusive work environment respecting diversity and offers reasonable accommodations for individuals with disabilities.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking an RA Professional Labeling for a one-year contract in Warsaw, Poland. The role involves coordinating translation activities of labeling documents and ensuring compliance with regulations while working within a collaborative, multicultural environment.
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Salary
Base: 95.000 PLN to 152.000 PLN annually; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
Coordination of translation activities
Quality check of labeling documents
Compliance maintenance of labeling documents
Communication with internal and external stakeholders
Implementation of standardization and new processes
Development of MEWA labeling documents
Knowledge of regional and global submission requirements
Nice-to-have
Experience in multi-cultural virtual environment
Knowledge of quality and supply chain impact
Intercultural sensitivity
Process optimization skills
Awareness of scientific principles (CMC, clinical, non-clinical)
Key Requirements
Bachelor's degree in scientific or equivalent field
Master’s degree preferred
Regulatory experience in drug development or marketed products
Detailed knowledge of local regulations and guidance
Fluent business and technical English communication
Ability to quickly acquire country-specific knowledge