QA Manager

Solvias seeks a QA Manager to oversee quality management software administration, lead cross-site projects, and ensure GMP compliance within an analytical-pharmaceutical setting.

This position focuses on the administration and enhancement of the company's quality management software while leading initiatives across different locations. The role ensures that digital systems support robust quality processes and regulatory standards.

Responsibilities

• Act as the system administrator for the quality management software platform.
• Provide user support and conduct training sessions for staff members.
• Refine and update internal processes, including the revision of standard operating procedures (SOPs) and related documentation.
• Standardize workflows to ensure consistency across operations.
• Lead various projects, often involving coordination between multiple sites.
• Deploy new modules and functionalities within the quality management software to enhance capabilities.

Requirements

• Educational background in analytical chemistry, biochemistry, or life sciences.
• Professional experience within the analytical-pharmaceutical sector, with prior quality assurance exposure preferred.
• Comprehensive understanding of GMP regulatory frameworks, including ICH, FDA, USP, and Ph. Eur. guidelines.
• Strong expertise in data integrity principles and risk assessment for computerized systems.
• Fluent command of the English language.

Nice to have

• Prior experience as a system administrator or advanced IT knowledge.
• Fluency in German.

About the company

Solvias fosters a collaborative environment where team members are encouraged to share their expertise and continuously develop their professional skills.

• Emphasis on teamwork and knowledge sharing among colleagues.
• Focus on personal and professional capability improvement.