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Looking to use your technical expertise to ensure QC equipment and systems remain inspection‑ready and future‑proof?

̽»¨ºÏ¼¯ is seeking a Senior QC Equipment Technical Specialist to support the lifecycle management of Quality Control equipment and electronic systems within a laboratory environment. This role involves ensuring compliance with current Good Manufacturing Practices and supporting technical developments, procurement, validation, and training activities.

Responsibilities:

• Manage and maintain QC laboratory systems and software to ensure compliance with cGMP and internal procedures.
• Lead qualification and validation processes for QC equipment and systems in line with industry standards.
• Support procurement and forecasting for new or replacement lab equipment and software.
• Develop and maintain procedures for system backup, archiving, and data retrieval.
• Troubleshoot and resolve technical issues, escalating as needed.
• Coordinate system updates and upgrades with external providers and internal IT teams.
• Provide training and guidance to QC team members on specialist equipment usage.
• Lead method transfer projects with third-party contract laboratories.
• Prepare and update Standard Operating Procedures (SOPs) and training materials.
• Generate reports and Key Performance Indicators (KPIs) related to system administration activities.
• Identify and implement continuous improvement opportunities for more efficient and compliant operations.
• Respond to global regulatory queries regarding equipment and methods.

Key Skills and Requirements:

• Strong knowledge of pharmaceutical QC equipment, electronic systems, and validation processes.
• Familiarity with Computer System Validation (CSV), GAMP guidelines, and data integrity principles.
• Proficiency in analytical software and electronic quality systems.
• Ability to interpret complex data and present findings clearly.
• Excellent communication and project management skills.
• Competence in Microsoft Office tools (Word, Excel, PowerPoint).
• Thorough understanding of GMP guidelines and regulations.
• Problem-solving, decision-making, and time management capabilities.
• Attention to detail and ability to work collaboratively within a team.

If you are having difficulty in applying or if you have any questions, please contact Molly Colclough at m.colclough@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

̽»¨ºÏ¼¯ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽»¨ºÏ¼¯ is acting as an Employment Agency in relation to this vacancy.

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