Digital Quality Engineer

Own the lifecycle management validation and sustained operation of digital quality systems and related capabilities. Serve as the Quality subject-matter expert and system owner for digital quality technologies ensuring solutions are compliant fit for purpose inspection-ready and aligned with cGMP data integrity and electronic records/electronic signatures requirements.

Responsibilities

• Lead Quality ownership of digital quality systems including implementation enhancement lifecycle management and operational support for quality-related capabilities. 

• Act as the Quality system subject-matter expert translating business cGMP data integrity and electronic records/electronic signatures requirements into clear system requirements and operational controls. 

• Partner with Quality Manufacturing IT Engineering Validation and other stakeholders to define configure test deploy and sustain compliant digital solutions. 

• Own or coordinate Quality input to software and computer system validation activities including risk assessments requirements test strategy test execution traceability defect resolution and validation deliverables as applicable. 

• Ensure systems and associated processes support accurate complete consistent contemporaneous and attributable electronic data and records throughout the data lifecycle. 

• Lead Quality review and approval of system changes releases access controls and periodic assessments through established change-control and quality-system processes. 

• Support investigation and resolution of system-related deviations incidents data-integrity events and CAPAs; assess product-quality and compliance impact and drive timely effective actions. 

• Develop and maintain procedures work instructions training materials and role-based training to promote compliant and effective use of digital quality systems. 

• Monitor system performance user feedback and emerging compliance needs; identify and implement continuous improvements in partnership with functional stakeholders. 

• Maintain inspection readiness by providing system expertise validation evidence traceability and clear responses to internal audits regulatory inspections and health-authority inquiries. 

Qualifications :

• Bachelors degree in engineering computer science life sciences or a related technical discipline; advanced degree preferred. 

• 5 years of relevant experience in pharmaceutical biotechnology or other regulated manufacturing environments including Quality Manufacturing digital systems or validation. 

• Experience with quality management systems electronic records systems manufacturing or laboratory systems or comparable GxP digital platforms strongly preferred. 

• Experience with software or computer system validation including risk-based validation requirements testing traceability and validation documentation preferred; ability to be accountable for validation activities as needed. 

• Excellent written and verbal communication skills with the ability to develop clear procedures training and inspection-ready documentation. 

• Ability to work independently prioritize effectively in a dynamic project environment and influence stakeholders without direct authority. 

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future. 
• We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of  any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

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Work :

No

Employment Type :

Full-time