Technical Writer

Lonza; Slough; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading life sciences company in Slough is seeking a dedicated Technical Writer to generate and revise GMP manufacturing documentation. The role involves collaboration with internal teams to ensure compliance and manage documentation quality. Ideal candidates have proven experience in GMP settings and strong communication skills. Join us to contribute to meaningful advancements in global health.

Qualifications

• Proven experience as a Technical Writer in GMP manufacturing.
• Ability to generate and revise detailed technical documentation.
• Knowledge of manufacturing regulations and standards.

Responsibilities

• Generate and revise GMP manufacturing documentation for technical accuracy.
• Provide technical support for process documentation.
• Maintain the Documentation Management System (DMS) as per procedures.
• Produce and process batch documentation for manufacturing.

Skills

Technical documentation generation

GMP compliance knowledge

Strong communication skills

Independent task management

Tools

Documentation Management System (DMS)

Job description

Technical Writer

Location: Slough

Are you ready to elevate your technical writing skills with a world-class company? Lonza AG is seeking a dedicated Technical Writer to join our Manufacturing team in the UK. This is an excellent opportunity to be part of a company that values innovation, collaboration, and the flawless execution of ideas that improve the world.

Key responsibilities:

• Generate and revise GMP manufacturing documentation for technical accuracy and compliance.
• Provide technical support for process documentation in collaboration with internal customers.
• Manage the creation and revision of GMP documents according to detailed procedures.
• Maintain the Documentation Management System (DMS) as per procedures.
• Produce and process batch documentation, ensuring timely review, approval, and availability for manufacturing.
• Monitor document creation progress and communicate with relevant parties to resolve issues.
• Manage quality records such as DCFs, Tasks, and CAPAs promptly.
• Contribute to the development and implementation of manufacturing procedures and work instructions.
• Support and train others during document revisions.
• Align with company policies, regulatory, and statutory requirements.

Key requirements:

• Proven experience as a Technical Writer in GMP manufacturing.
• Ability to generate and revise detailed technical documentation.
• Knowledge of DMS and documentation methodologies.
• Ability to manage multiple tasks independently.
• Strong communication skills for collaboration.
• Adherence to timelines and schedules.
• Experience with maintaining documentation quality records.
• Knowledge of manufacturing regulations and standards.
• Proactive, ambitious, and team-oriented attitude.

Join us in making a meaningful difference in the life sciences industry with your expertise and passion!

At Lonza, our products impact millions positively. We value ethics, respect, and environmental protection. We challenge and inspire our team to solve complex problems and develop innovative solutions, contributing to global health and well-being.