Manpower Life Sciences for TETHIS SPA
We are looking for a skilled scientific technical writer to join Tethis’ Quality and Regulatory Affairs office to contribute to creating and maintaining technical documentation and internal procedures.
Key Responsibilities:
- Gather and select information from internal and external sources
- Discuss with all internal personnel to assess relevant information and process structures
- Draft and proofread new technical documentation and update existing one, under the supervision of Area Management
- Write documentation in a user-oriented language style and graphics
- Create clear, synthetic, and complete documentation
Ideal Candidate Profile:
- Technical-scientific bachelor's degree
- Good writing skills
- Proficient Italian and English knowledge, both written and oral
- Proficient use of Microsoft Office Suite
- Preferably, courses on ISO 13485 standard and IVDR technical documentation drafting
Preferred Experience:
- 1-3 years’ experience in drafting technical manuals, technical files documentation, and quality procedures
- Working in highly regulated industries (IVD or MD preferred)
Key Skills:
- Logical thinking
- Accuracy
- Collaborative approach
Flexibility and adaptability
- Ability to understand other processes and people's needs
- Ability to communicate with people with different mindsets
- Self-training ability
Location: Milan
Contract: Permanent Position, CCNL Chimico Farmaceutico, remote work flexibility according to company policies after at least a 6-months coaching period.