Senior Equipment Qualification Specialist
2 weeks ago
The ideal candidate for this role will be responsible for managing the qualification, calibration, and routine maintenance of laboratory systems in a cGMP Quality Control environment. The successful individual will oversee tracking and management of activities through CMMS Maximo, author and approve validation life cycle documents for computer-related systems, ensure data integrity compliance, and execute approved protocols.
">- Bachelor's degree in a Science related field is required.
- Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation and data integrity assessments.
- Detailed knowledge of the methodology, instrumentation, and analytical techniques used for biopharmaceutical testing.
- Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record integrity.
- Demonstrated success in managing an equipment qualification or maintenance program advantageous.
Joining our organization as a Senior QC Associate will provide you with a unique opportunity to work in a fast-paced, dynamic environment where you can grow your career. You will have the chance to collaborate with talented professionals from various backgrounds and gain valuable experience in laboratory equipment validation and maintenance.
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