Job responsibilities:
- upgrading existing registration documentation for veterinary pharmaceutical products,
- processing registration documentation related to requests for text changes and extension of registration authorization,
- preparing registration documentation for expert review by state authorities,
- collaboration with expert reviewers,
- creating texts for product information summaries, package inserts, and packaging,
- preparing materials on issues related to pharmaceutical product registration,
- collaboration with EU regulatory authorities in procedural matters.
We require:
- degree in: veterinary medicine, general medicine, pharmaceutical sciences, biology, biochemistry, microbiology, or chemistry,
- knowledge of applicable regulations,
- strong computer skills,
- responsibility and precision, ability to work in teams,
- organizational skills.
An advantage (not required):
- experience with registration documentation in the veterinary pharmaceutical field, including related legislation,
- communicative proficiency in English.
We offer:
- opportunities for further education and professional growth,
- training with significant self-study component,
- backing of a dynamically developing company operating on markets worldwide,
- space for those who want to accomplish something,
- interesting, creative, and responsible work,
- development of practical skills and professional expertise,
- mobile phone, possibility of partial home office, and additional employee benefits (meal vouchers, gift vouchers, monthly attendance bonus).
Required education: university / higher education.
Required language: English (intermediate).
Salary: from 30,000 Kč/month. In case of candidate's experience with registration documentation in the veterinary pharmaceutical field, including related legislation, we offer up to 50,000 Kč/month.
Benefits: meal vouchers, gift vouchers, monthly attendance bonus.
Type of employment: full-time / part-time position.
Length of employment: fixed-term contract.Job responsibilities:
- upgrading existing registration documentation for veterinary pharmaceutical products,
- processing registration documentation related to requests for text changes and extension of registration authorization,
- preparing registration documentation for expert review by state authorities,
- collaboration with expert reviewers,
- creating texts for product information summaries, package inserts, and packaging,
- preparing materials on issues related to pharmaceutical product registration,
- collaboration with EU regulatory authorities in procedural matters.
We require:
-…