Drive quality assurance as a Quality Management System Coordinator with a focus on SOPs and document control. This hybrid full-time role provides vital support to regulatory compliance and internal training initiatives.
In this permanent full-time position, you'll manage the drafting and maintenance of SOPs in alignment with regulatory and internal guidelines. You'll coordinate training for Production and Quality staff while participating in continuous improvement initiatives. This role offers a collaborative environment with a Monday to Friday schedule from 8:00 am to 4:30 pm, adaptable to your needs.
Key Responsibilities:
• Draft and maintain documentation per approved templates
• Support GMP documentation-related improvements
• Assist with Quality Assurance audits and initiatives
• Manage efficiency in document reviews and approvals
• Adhere to established SOPs and Good Pharmacovigilance Practices
Requirements:
• Minimum 2 years of document control experie...