Job Summary:
We are seeking a highly skilled Quality Control Associate to join our team. In this role, you will be responsible for planning, executing and documenting the qualification, calibration and routine maintenance of laboratory systems in our cGMP Quality Control laboratory facilities.
Main Responsibilities:
* Manage and coordinate schedules of Calibration Technicians ensuring that all maintenance and calibration activities are tracked and managed through the Computerised Maintenance Management System (CMMS).
* Author Validation Life Cycle documents for computer related systems including Data Integrity testing and business administration of Laboratory Computer Related systems.
* Commission new laboratory equipment and facilities developing lab equipment specifications.
* Write equipment validation protocols and associated summary reports.
* Conduct periodic reviews of instrument validation as part of validation life cycle.
* Act as subject matter expert on instrument validation regulations and procedures.
* Serve as point of contact with laboratory equipment vendors and engineers.
* Coordinate equipment repairs and maintenance with vendors/contractors and carry out equipment maintenance as required.
* Write/equipment operating procedures and manuals.
* Design and conduct training for QC staff and other department staff as applicable.
* Project manage Change controls and adhere to Change Control metrics.
We offer a range of benefits, including:
* A competitive salary package
* Ongoing professional development opportunities
* A dynamic and supportive work environment
Please note that this is a full-time position, working Monday to Friday with occasional overtime.
If you have a passion for quality control and a drive to succeed, we encourage you to apply for this exciting opportunity!