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We are seeking an experienced Validation Specialist to support validation activities within a state-of-the-art aseptic manufacturing facility. This role will focus on ensuring GMP compliance across critical manufacturing systems, equipment, facilities, and processes involved in sterile drug product manufacturing.The successful candidate will work ...
We are seeking an experienced Validation Specialist to support validation activities within a state-of-the-art aseptic manufacturing facility. This role will focus on ensuring GMP compliance across critical manufacturing systems, equipment, facilities, and processes involved in sterile drug product manufacturing.The successful candidate will work c...
We are seeking an experienced Validation Specialist to support validation activities within a state-of-the-art aseptic manufacturing facility. This role will focus on ensuring GMP compliance across critical manufacturing systems, equipment, facilities, and processes involved in sterile drug product manufacturing.The successful candidate will work c...
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Completes transducer repairs according to work instructions and quality procedures, including working with repair team to perform all repairs against due dates and lab metricsMaintains probe files and accurately documents probe repair process including, but not limited to, recording interim quality checks and/or any issues with repairReports proble...
Perform incoming inspection of TEE probes to assess mechanical, electrical, and imaging defectsConduct functional testing using OEM or third-party test equipment to isolate root cause (array faults, cable/strain relief damage, bending section issues, leakage current failures)Document defect findings and correlate with intake photos/notes to support...
Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...