SCIENTIFIC TECHNICAL WRITER

TN Italy; Milano; Ibrido; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading company in the life sciences sector is seeking a skilled scientific technical writer to join their Quality and Regulatory Affairs office. The role involves creating and maintaining technical documentation, requiring strong writing skills and a technical-scientific background. The ideal candidate will have experience in regulated industries and be proficient in both Italian and English. Flexibility for remote work is offered after an initial coaching period.

Competenze

• 1-3 years’ experience in drafting technical manuals and quality procedures.
• Experience in highly regulated industries (IVD or MD preferred).

Mansioni

• Gather and select information from internal and external sources.
• Draft and proofread new technical documentation.
• Create clear and complete documentation.

Conoscenze

Writing

Logical thinking

Accuracy

Collaboration

Flexibility

Formazione

Technical-scientific bachelor's degree

Strumenti

Microsoft Office Suite

Descrizione del lavoro

Collaborative approach

Flexibility and adaptability

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:

1. Gather and select information from internal and external sources
2. Discuss with all internal personnel to assess relevant information and process structures
3. Draft and proofread new technical documentation and update existing ones, under the supervision of Area Management
4. Write documentation in a user-oriented language style and graphics
5. Create clear, synthetic, and complete documentation

Ideal Candidate Profile:

1. Technical-scientific bachelor's degree
2. Good writing skills
3. Proficient in Italian and English, both written and oral
4. Proficient use of Microsoft Office Suite
5. Preferably, courses on ISO 13485 standard and IVDR technical documentation drafting

Preferred Experience:

1. 1-3 years’ experience in drafting technical manuals, technical files documentation, and quality procedures
2. Experience working in highly regulated industries (IVD or MD preferred)

Key Skills:

1. Logical thinking
2. Accuracy
3. Collaborative approach
4. Flexibility and adaptability
5. Ability to understand other processes and people's needs
6. Ability to communicate with people with different mindsets
7. Self-training ability

Location: Milan

Contract: Permanent Position, CCNL Chimico Farmaceutico, remote work flexibility according to company policies after at least a 6-month coaching period.