Senior Scientific Writer at AtomVie

Elevate your career as a Senior Scientific Writer with Atom Vie, focusing on process development in the pharmaceutical sector. This role demands experience in technical documentation and collaboration across diverse teams.

The Scientific and Technical Writer position at Atom Vie requires advanced-level skills in writing and managing GMP documentation. With a minimum of 3 years in a pharmaceutical GMP environment, you must engage with process chemists, scientists, and manufacturing operators on vital documentation. Your attention to detail and scientific judgment will be crucial as you navigate documentation for clinical supply programs and radiopharmaceutical manufacturing.

Key Responsibilities:

• Author and manage SOPs, master batch records, and CAPAs

• Ensure GMP compliance in all documentation activities

• Coordinate document development with cross-functional stakeholders

• Prepare internal and client-facing documentation summaries

• Support equipment validation documentation and related tasks

Requirements:

• Master’s degree in Chemistry or Chemical Engineering

• 3+ years of experience in pharmaceutical GMP

• Proven scientific writing expertise and communication skills

• Understanding of GMP regulations and practices

• Ability to work independently in a cross-functional team

Leverage your scientific writing skills to support Atom Vie’s innovative processes in a collaborative work environment.
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