QC Equipment Lifecycle Specialist — Validation & Compliance

Spectraforce Technologies, Inc.

Harvard (MA)

On-site

USD 70,000 - 105,000

Full time

6 days ago

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Job summary

Spectraforce Technologies, Inc. in Devens, MA seeks a QC Equipment Lifecycle Specialist to support validation, calibration, and maintenance of QC laboratory equipment in a GMP setting. The role interfaces with QC SMEs, site engineering, facilities, and vendors for lifecycle activities and procedure updates.

The specialist will maintain records, assist investigations, and ensure data integrity and compliance across analytical and microbiology QC labs.

Qualifications

Experience in GMP environments with instrument qualification.
Ability to understand and apply global GMP requirements accurately.
Detail-oriented with strong problem solving.
Ability to work independently in a fast-paced team.
Strong written and verbal communication with cross-functional peers.
Working knowledge of biomolecular equipment is preferred.
2+ years of relevant regulated-ex environment experience.

Responsibilities

Collaborate with QC labs and other departments to validate, calibrate, maintain QC equipment.
Maintain equipment records per GMP procedures.
Keep electronic equipment database and logs up to date.
Assist management with investigations and deviations related to equipment.
Perform tasks to support QC laboratories as required.