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QA Executive Level II - Job Opportunity at Viatris (Mylan Teoranta)

Inverin, Ireland
Full-time
Mid-level
Posted: February 5, 2025
On-site
EUR 45,000 - 65,000 per year based on Irish pharmaceutical industry standards and role requirements

Benefits

Competitive salary with performance bonus scheme
Comprehensive health insurance coverage
Strong pension plan
Career development and progression programs
Work-life balance initiatives

Key Responsibilities

Lead quality assurance batch record review for finished pharmaceutical products
Manage incident reporting and CAPA systems
Oversee technical quality review for product artwork and packaging
Direct quality oversight of packaging operations
Coordinate customer quality complaints and medical device vigilance
Generate quality metrics and annual product quality reviews
Maintain inspection programs and quality training initiatives

Requirements

Education

Bachelor's degree in Science related discipline

Experience

2-4 years relevant pharmaceutical experience with 1 year in Quality Assurance

Required Skills

Knowledge of quality system aspects (Deviation management, CAPA, complaint handling, auditing, change management, supplier qualification, batch release) Experience with Trackwise or similar electronic document management systems (preferred) Excellent communication skills Strong organizational and time management abilities Proficiency in Microsoft Office suite Experience in sterile manufacturing (preferred)
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on quality assurance in pharmaceutical manufacturing due to stringent regulatory requirements and complex supply chains Growing adoption of electronic quality management systems and digital documentation processes Rising importance of medical device vigilance and post-market surveillance Emphasis on end-to-end quality oversight from raw materials to finished products

Role Significance

Typically part of a 5-10 person quality assurance team in medium to large pharmaceutical manufacturing facility
Mid-level management role with significant responsibility for quality compliance and product release decisions

Key Projects

Implementation and optimization of quality management systems Regulatory compliance initiatives and audit preparation Process improvement and deviation reduction programs Training program development and delivery

Success Factors

Strong technical understanding of pharmaceutical manufacturing processes Ability to balance quality requirements with operational efficiency Excellence in documentation and attention to detail Strong interpersonal skills for cross-functional collaboration

Market Demand

High demand position due to expanding pharmaceutical manufacturing presence in Ireland and increasing quality compliance requirements

Important Skills

Critical Skills

Quality system management expertise due to regulatory focus Technical document review capabilities for product release Communication skills for cross-functional collaboration Data analysis for quality metrics and trending

Beneficial Skills

Experience with electronic quality management systems Knowledge of GDP and GMP regulations Project management capabilities Risk assessment and mitigation skills

Unique Aspects

Role combines traditional QA responsibilities with modern quality management systems
Position offers exposure to both sterile and non-sterile manufacturing processes
Opportunity to work in a global pharmaceutical organization with significant growth potential

Career Growth

2-4 years in current role before progression, depending on performance and organizational growth

Potential Next Roles

Senior QA Manager Quality Systems Manager Validation Manager Quality Operations Director

Company Overview

Viatris (Mylan Teoranta)

Global pharmaceutical company formed through the merger of Mylan and Upjohn, focusing on both generic and branded medications

Major player in global generic pharmaceutical manufacturing with significant presence in specialty medications
Strategic manufacturing location in Ireland serving European and global markets
Professional environment with strong emphasis on compliance, quality, and continuous improvement
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