Electronic quality management system jobs

Product Assurance Complaint Analyst

HISTOSONICS INC · Posted Nov 11, 2026

HISTOSONICS INC · Posted Nov 11, 2026

Thermo Fisher Scientific · Posted Nov 10, 2026

Responsible for investigating, documenting, and resolving manufacturing deviations in a sterile pharmaceutical environment.

Author and support deviation investigations associated with sterile pharmaceutical manufacturing operations within Building 16
Develop clear, accurate, and comprehensive investigation reports that document the sequence of events, investigation findings, impact assessments, root cause analysis, corrective actions, and conclusions
Gather and evaluate information from manufacturing batch records, equipment logs, electronic systems, procedures, and other relevant documentation
Conduct interviews with manufacturing personnel and subject matter experts to establish factual event timelines and support investigation findings
Collaborate with cross-functional teams to identify potential contributing factors and determine appropriate investigation scope

Associate's degree in a scientific, technical, engineering, or related discipline with 1 year relevant experience
Bachelor's degree in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or a related field preferred
Nice to have: pharmaceutical
Nice to have: biotechnology
Nice to have: sterile manufacturing environments

Labcorp · Posted Nov 9, 2026

Oversee GMP equipment lifecycle and support quality compliance in a biopharmaceutical environment.

Oversee the full GMP equipment lifecycle, including onboarding, qualification, maintenance, calibration, and retirement.
Coordinate equipment activities with internal stakeholders, service providers, and approved vendors.
Serve as the equipment Subject Matter Expert (SME), providing technical support and resolving equipment-related issues.
Ensure equipment compliance with GMP regulations, internal procedures, and quality standards.
Own or support deviations, CAPAs, change controls, investigations, and audit responses related to equipment.

Bachelor's degree in a scientific, engineering, or related discipline
Nice to have: Experience supporting BioPharm, CMC, laboratory, or manufacturing operations
Nice to have: Knowledge of equipment qualification and validation (IQ/OQ/PQ)
Nice to have: Experience with electronic quality or maintenance management systems
Nice to have: Familiarity with System Lifecycle (SLC) processes