QC Systems & Equipment Specialist
Quality Control | GMP Environment | Life Sciences
In order to make an application, simply read through the following job description and make sure to attach relevant documents.
We are currently seeking a QC Systems & Equipment Specialist to support Quality Control laboratory equipment and associated electronic systems across their full lifecycle within a regulated GMP environment.
This role plays a key part in ensuring QC systems and software used to support the manufacture, packaging, testing, storage, and distribution of marketed pharmaceutical products remain compliant with current GMP and corporate quality expectations.
Key Responsibilities
- Support the lifecycle management of QC laboratory equipment and electronic systems, including ongoing technical developments and third‑party contractor activities
- Ensure QC systems and software operate in compliance with cGMP, GxP, and internal SOP requirements
- Contribute to the writing, review, and approval of quality policies, procedures, and system documentation
- Support and deliver qualification and validation activities for QC equipment, processes, and electronic systems in line with GMP and GAMP guidelines
- Lead the maintenance and continuous improvement of Qualification and Validation procedures, ensuring alignment with current regulatory expectations
- Support the procurement of new laboratory equipment and software, including forecasting for replacements and upgrades
- Coordinate and lead equipment servicing, maintenance, and repair activities
- Provide training and technical support to QC team members on specialist equipment and systems
- Manage user access, change control, and system data configuration to ensure continuous availability and functionality of QC systems
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Key Skills & Experience
- Experience supporting QC laboratory equipment and electronic systems within a regulated environment
- Strong understanding of GMP, GxP, and validation principles
- Familiarity with qualification, validation, and system lifecycle management
- Experience working cross‑functionally with QC, QA, engineering, and third‑party service providers
- Strong documentation skills with the ability to work to inspection‑ready standards
- Proactive, organised, and able to manage multiple priorities in a regulated setting