Technical Writer Vacancy | Alvotech | Regulatory & Scientific Documentation

Apply now for Technical Writer role at Alvotech. Openings for science graduates with regulatory and scientific writing expertise. Deadline: Sept 25, 2025.

Alvotech, a global biopharmaceutical company specializing in biosimilars, is seeking a skilled Technical Writer to join its dynamic team in India. This is a full-time opportunity for science graduates with a passion for clear scientific communication and regulatory documentation. If you enjoy translating complex scientific data into structured, accurate, and regulatory-compliant content, this role is ideal for you.

Company Overview

Alvotech is dedicated to improving access to affordable biologic medicines through innovation in biosimilars. With state-of-the-art facilities, a global presence, and a strong commitment to integrity, diversity, and sustainability, Alvotech is one of the fastest-growing biopharmaceutical companies in the world. The company fosters a collaborative, inclusive culture where employees thrive while contributing to healthcare solutions that impact patients worldwide.

Job Role & Responsibilities

As a Technical Writer at Alvotech, you will:

• Prepare Regulatory and Technical Documentation: Draft briefing books for health authority interactions, Module 3 dossiers, quality assessments, risk ranking reports, and validation protocols.
• Collaborate Across Teams: Work with internal stakeholders such as Pharmaceutical Sciences, Program Management, Quality Control, Manufacturing, and Regulatory Affairs.
• Content Development & Editing: Research, structure, and revise documentation, ensuring clarity, compliance, and alignment with regulatory expectations.
• Engage Subject Matter Experts (SMEs): Source and synthesize technical information independently from SMEs.
• Template Management: Apply and maintain templates to ensure document consistency and efficiency.
• Dossier Translation: Convert source material into high-quality regulatory dossier content.

Eligibility / Qualifications

• Education: B.Sc. in a scientific discipline (Biotechnology preferred).
• Experience:
  • Proven experience in technical report writing.
  • Experience in regulatory document writing (Module 3) is highly desirable.
• Technical Skills:
  • Strong scientific background with data gathering, summarizing, and evaluation skills.
  • Proficiency in MS Word and Excel; knowledge of Prism (GraphPad) and JMP is an advantage.
• Additional Knowledge: Understanding of antibody/protein structure and protein manufacturing processes (cell line, upstream/downstream, drug product development, or protein analytics) is beneficial.
• Soft Skills: Excellent multitasking, ability to work independently and cross-functionally, flexible attitude, and strong communication skills.

Location & Deadline

• Location: India (Full-time position).
• Application Deadline: September 25, 2025.

Benefits & Perks

• Inspiring projects with global impact on patient access to biologics.
• International work culture fostering diversity, inclusion, and collaboration.
• Positive, flexible, and innovative work environment.
• Training opportunities and clear career progression.
• Work-life balance supported with home internet and home office equipment.
• Global exposure within a fast-growing biopharma company.

Application Process

Interested candidates can apply directly through the official career portal:
Apply Here

Why Join Alvotech?

• Work with a global leader in biosimilars and biopharma innovation.
• Be part of an international team driven by purpose and integrity.
• Access career development opportunities and continuous learning.
• Contribute to affordable and accessible biologic medicines that improve patient lives worldwide.

FAQs

1. What documents will a Technical Writer at Alvotech prepare?
Regulatory dossiers, briefing books, protocols, validation reports, and scientific assessments.

2. Who can apply for this role?
Graduates with a B.Sc. in Biotechnology or related sciences and proven technical writing experience.

3. Is prior experience in regulatory writing necessary?
Yes, prior experience in regulatory document writing, especially Module 3 dossiers, is preferred.

4. Where is the position based?
The position is based in India with full-time employment.

5. What is the deadline for applications?
The deadline is September 25, 2025.

Call to Action

Take your career to the next level with Alvotech. Apply now to become a Technical Writer and help deliver life-changing biosimilars to patients worldwide. Submit your application before the deadline to secure your opportunity!

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