Are you a seasoned SOP writer with a knack for navigating the intricacies of Good Manufacturing Practices (GMP) and commercial product standards? If so, we have an exciting opportunity for you!

We are on the lookout for a highly skilled Interim SOP Writer to join a dynamic team on a fully remote basis for a minimum 3-month contract. As an SOP Writer, you will play a crucial role in ensuring their processes align with regulatory requirements, uphold product quality, and respond effectively to recalls and complaints.

Key Responsibilities:

• Develop and refine Standard Operating Procedures (SOPs) in compliance with GMP standards and industry best practices.
• Collaborate with cross-functional teams to gather input and insights for SOP development and updates.
• Conduct thorough research and analysis to ensure SOPs reflect current regulations and guidelines.
• Utilise your expertise in product quality to enhance SOPs and drive continuous improvement initiatives.
• Assist in the development of protocols and procedures for handling product recalls and customer complaints.
• Maintain accurate documentation and version control for all SOPs and related materials.

Requirements:

• Proven experience as an SOP writer in a GMP-regulated environment, within the pharmaceutical or biotech industry.
• Deep understanding of GMP regulations and their application to commercial product manufacturing.
• Strong knowledge of product quality standards, including experience with quality control processes and methodologies.
• Familiarity with product recall procedures and customer complaint management.
• Self-motivated and capable of working independently in a remote environment..

If you’re ready to take on a challenging and rewarding role as an Interim SOP Writer, apply now and help uphold the highest standards of quality and compliance in our operations!

Please apply directly or call for more information.