QC Equipment Specialist: Calibration, Troubleshooting & GMP

Actalent; Norwood (MA); Presencial; USD 47.000 - 50.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical

Dental & vision

Critical Illness

401(k)

Life Insurance

Short & long-term disability

HSA

Transit benefits

Employee Assistance Program

Paid time off

Descripción de la vacante

Actalent is seeking a QC Equipment Support professional for Norwood, MA. This contract role focuses on investigating equipment failures, maintaining calibration, and supporting quality systems records including deviations and CAPAs.

On-site responsibilities include assisting with non-invasive UHPLC repairs and coordinating with Facilities, Metrology, and QC to minimize downtime. The ideal candidate has a Bachelor's in sciences with 2–5 years of industry experience and 5 years of BS or 2+ GMP QC

Formación

• Bachelor's degree required; 2-5 years of industry experience preferred.
• 5 years with BS or 2+ GMP QC lab experience required; ability to learn GxP.

Responsabilidades

• Support team to investigate and resolve issues related to equipment failures, system deficiencies, deviations, and equipment troubleshooting.
• Support authoring quality systems records such as deviations, change controls, CAPAs, OOTs (Out of Tolerance) as required.
• Assist with on-site QC Equipment team activities and inventory management for equipment consumables and accessories.
• Coordinate and schedule calibration/maintenance with Facilities, Metrology, and QC to minimize downtime.
• Review preventative maintenance reports, calibration certifications, CMMS records, and perform system inventory audits.

Conocimientos

Lab equipment

IQ/OQ

Quality control

Metrology

Validation testing

CAPA

HPLC

Calibration

Chemistry

CMMS

Troubleshooting

Equipment troubleshooting

Educación

Bachelor's degree in sciences

Descripción del empleo

Actalent is seeking a QC Equipment Support professional for Norwood, MA. This contract role focuses on investigating equipment failures, maintaining calibration, and supporting quality systems records including deviations and CAPAs.

On-site responsibilities include assisting with non-invasive UHPLC repairs and coordinating with Facilities, Metrology, and QC to minimize downtime. The ideal candidate has a Bachelor's in sciences with 2–5 years of industry experience and 5 years of BS or 2+ GMP QC