Instrument Lifecycle Specialist QC/Mfg; cGMP) On Site
Listed on 2026-10-08
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
Pfizer is seeking a System Specialist to support instrumentation lifecycle activities within cGMP Quality Control and Manufacturing at the Andover site. You will ensure instrument integrity, perform troubleshooting, and collaborate with QC Lab and Manufacturing teams to maintain compliant systems.
The role requires a bachelor's degree with 2+ years of experience in regulated hardware/software, strong documentation skills, and the ability to handle periodic off-hours support as needed.
We are seeking a motivated Instrument Lifecycle Specialist QC/Mfg (cGMP) On Site to join Scorpion Therapeutics in Andover, MA, United States.
The Instrument Lifecycle Specialist QC/Mfg (cGMP) On Site role at Scorpion Therapeutics is now open for applications in Andover, MA, United States.
Join us at Scorpion Therapeutics as our next Instrument Lifecycle Specialist QC/Mfg (cGMP) On Site in Andover, MA, United States.
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