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Shift QA Specialist

GE HEALTHCARE -
Cork, County Cork

Apply Now

Job details

Qualifications

Engineering
English

Full job description

Job Description Summary

As a Shift QA Specialist at GE HealthCare, you will play a key role in ensuring the highest quality and compliance standards across our manufacturing operations. Working closely with Operations, QC, and cross-functional teams, you will drive quality excellence, support batch release activities, proactively identify and resolve quality issues, and help ensure our life-saving products are delivered safely and compliantly to patients around the world.

GE HealthCare's Pharmaceutical Diagnostics (PDx) segment develops and manufactures contrast media and radiopharmaceutical imaging agents used across X-ray/CT, MRI, ultrasound, SPECT and PET. PDx products support diagnostic pathways in neurology, cardiology and oncology, are used by healthcare professionals in more than 130 countries, and support approximately 140 million patient procedures each year - equivalent to four procedures every second.

Job Description

Responsibilities

Ensure compliance with GMP, GE Healthcare Corporate Standards, Quality Management System (QMS), site policies/procedures, regulatory requirements and industry standards
Represent Quality at Tier 1&2 meetings (Operations and QC) providing updates and communicating any concerns, escalations and ensuring any quality compliance related actions are tracked at the Tiers.
Support spot checks on GMP/ GDP review into documentation through GEMBA check/ review/ advise to standards highlighting focus areas such as cleaning standards, PIR, documentation completion etc
Complete batch record reviews for QA as required
Provide governance oversight for the housekeeping GEMBA process and walkthroughs in QC and Operations driving compliance to processes and procedures ensuring focus on cGxP mindset. Coordinate walks with QC and operations and support functions. Document, communicate and track completion of action items, trend and escalate. Holding area owner accountable and responsible for raising SR’s and completion of tasks.
Ownership for Instruction Monitoring process governing monthly meetings to review monthly data and any trending of issues to ensure operations actions are assigned.
Provide support for escalations as QA primary point of contact in operations in general troubleshooting and problem solving, providing technical direction and guidance to support overall business needs, which may result in Deviation/ Investigation support, escalation and containment
Lead & support cross functional/continuous improvement teams as required to provide consultative and collaborative support on quality related issues
Lead & support investigation root cause and resolution ensuring appropriate CAPA actions implemented to prevent recurrence where relevant
Review, author, manage change, authorise relevant documentation types to include, but not limited to; SOPs, investigations, commitments (Regulatory Agency, investigation, audit, etc.), change controls, forms, logbooks, validation and batch release documentation
Provide Quality support for shutdown actions and activities to ensure areas shutdown and start back up compliantly
Lead & support management of relevant metrics/forums to ensure ownership and delivery of, and compliance with, key site metrics
Maintain up-to-date knowledge of pharmaceutical legislation and industry best practice.

Qualifications and experience

3rd level qualification in Science / Engineering discipline or equivalent knowledge or experience
Significant experience within a GMP / QA environment in a pharmaceutical company or similar regulated environment
Eligible to act as a Qualified Person in line with local and EU directives.

Desired Skills

Ability to create and maintain effective interpersonal relationships with all levels of personnel within all cross functional departments in the organization
Excellent communication, negotiation and risk-based decision-making skills, promoting openness, dialogue and collaboration
Results oriented with a strong ability to effectively troubleshoot, and problem solve issues
Promote a continuous improvement culture.

Eligibility requirements

A good level of English and a valid work permit

Inclusion & Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities.

Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.

#LI-BG1

Additional Information

Relocation Assistance Provided: No

Apply Now

Refine Your Search

manufacturing specialist jobs in county cork

Shift QA Specialist

Senior Operations Planning Specialist

Sr. Associate Quality Systems Specialist

Site Safety Specialist

Senior Specialist - Industry 4.0 & Manufacturing Data

HSE Specialist

Quality Assurance Specialist

Material Science Technical Specialist-Hybrid

Talent Acquisition Specialist

Process Safety Expert

Laboratory Systems Integration Specialist

Fabrication Draftsperson

R&D Project Manager

Principal Industrial Designer

IT Validation Specialist

Eirdata Electrical Site Lead

Environmental Health and Safety Specialist – Cork

2027 Tax Graduate Programme - Cork

Rigid Lorry / Truck Driver Carrigaline & Water Street Branch

Global Operational Technology Engineer

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