Find Quality control associate Jobs in County Dublin

Senior Associate, Global Risk Management Programs
Azurity Pharmaceuticals - US —Dublin, County Dublin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
10h
ERP Technical Delivery Manager
PM Group —Dublin, County Dublin
- Oracle
- Computer Science
- ERP systems
Senior Human Resources Associate
International Organization for Migration —Dublin, County Dublin
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Spanish
10d
Associate Mechanical Engineer
EDC Engineering Design Consultants LTD. —Dublin, County Dublin
- €60,000–€80,000 a year
- Overtime
- Hybrid work
- Engineering
- Microsoft Office
- Master's degree
- Annual leave
- Work from home
Quick apply
14d
Internal Audit Associate Director
Davy —Dublin, County Dublin
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Analysis skills
- Employee assistance program
Quick apply
4d
Basic grade Cardiac Physiologist Permanent
Tallaght University Hospital —Tallaght, County Dublin
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
- Sick pay
4d
Associate Director - Enterprise Risk Management
Waystone —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Office
- Finance
- Analysis skills
Quick apply
External Manufacturing Technical Lead – Large Molecule Drug Substance
MSD —Leopardstown, County Dublin
- Full-time
- Hybrid work
- Engineering
- English
- Analysis skills
2h
Tax Risk & Controversy Senior Associate
PwC —Dublin, County Dublin
- Full-time
Senior Process Engineer
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Data analysis skills
- Bachelor's degree
Assistant Manager - Dundrum Town Centre, Hollister
A&F Hollister Ireland Limited —Dublin, County Dublin
- €38,000 a year
- Full-time
- Sales
- English
- Supervising experience
- Store discount
- Annual leave
Senior Associate - Fund Accounting
StepStone Group —Dublin, County Dublin
- Microsoft Excel
- Customer service
- Microsoft Office
Director of Food & Beverage
Marriott International, Inc —Dublin, County Dublin
- Full-time
- Culinary experience
- Restaurant management
- Hotel
Senior Process Engineer - Packaging
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Data analysis skills
- Bachelor's degree
Key Lead - Dundrum Town Centre, Hollister
A&F Hollister Ireland Limited —Dublin, County Dublin
- €16.50 an hour
- Part-time
- Management
- Sales
- Supervising experience
- Store discount
Asset & Wealth Management, Business Controls, Associate, Dublin
Goldman Sachs —Dublin, County Dublin
- Full-time
- Finance
- Organisational skills
- In-person
- Employee assistance program
Global Financial Crimes Manager
Bank of America —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Employee assistance program
9h
Associate Director, Biostatistics
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Master's degree
Senior Internal Auditor, Technology - Dublin or Amsterdam
CRH Group Services Ltd. —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Computer Science
- Analysis skills
Quick apply
Accountant FTC
PwC —Dublin, County Dublin
- Full-time
- Finance
- Analysis skills
- Bachelor's degree

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Senior Associate, Global Risk Management Programs

Azurity Pharmaceuticals - US
Dublin, County Dublin

Apply Now

Job details

10 hours ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
English
Microsoft Office
Master's degree
Bachelor's degree
Communication skills
Adobe Acrobat

Full job description

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

Brief team/department description:

The Medical Affairs Group at Azurity is hiring a highly motivated Drug Safety Associate to join the team. This individual will report to the Vice President, Global Drug Safety and will support Pharmacovigilance activities across the organization. This individual will leverage existing industry knowledge, organizational and communication skills to support ongoing drug safety initiatives while maintaining compliance.

Principle Responsibilities:

Support implementation, execution, and maintenance of global risk management programs, including REMS (US), RMPs/PPP (EU), and other region-specific risk minimization activities.
Assist in development and maintenance of procedures, training materials, and operational workflows supporting pharmacovigilance and risk management programs. · Monitor program effectiveness by tracking key metrics, patient education activities, and healthcare provider compliance controls.
Support management of program deviations, CAPAs, and inspection readiness activities to ensure regulatory compliance.
Coordinate with internal teams and external vendors to support administration of risk management programs and patient support services.
Assist in preparation for health authority inspections, audits, and responses related to risk management activities.
Support development, review, and maintenance of Risk Management Plans (RMPs) in alignment with global regulatory requirements and evolving safety data.
Coordinate cross-functional input from safety, regulatory, and medical teams to support risk assessment and risk minimization activities.
Track regulatory commitments, milestones, and deliverables associated with RMPs and risk management programs.
Collaborate with signal detection and aggregate reporting teams to support incorporation of emerging safety data into RMP updates.
Assist in preparation of regulatory submissions and responses related to pharmacovigilance and risk management commitments.
Support pharmacovigilance planning and execution for product launches, including tracking timelines, deliverables, and cross-functional dependencies.
Assist in ensuring PV system readiness across all lifecycle phases (Build, Submission, and Post-Launch).
Identify and escalate potential risks that may impact compliance or regulatory timelines.
Coordinate responses to safety-related inquiries from internal stakeholders and regulatory authorities.
Maintain project plans and trackers to support PV programs, ensuring accurate tracking of milestones, deliverables, and dependencies.
Provide routine updates on timelines, risks, and progress to internal stakeholders.
Collaborate cross-functionally to ensure alignment on priorities, timelines, and deliverables across PV programs.
Participate in cross-functional meetings and governance forums supporting pharmacovigilance initiatives.
Support continuous improvement initiatives by identifying process gaps and contributing to development of standardized tools and workflows.
Assist in documenting and implementing process improvements to enhance compliance, efficiency, and consistency across PV operations.

Qualifications and Education Requirements

Bachelor’s or master’s degree in life science or healthcare-related field OR equivalent combination of education and experience (i.e., an information science degree with at least 3 years of relevant working knowledge of supporting drug and patient safety)
At least 3 years of experience reviewing individual case reports, aggregate reports and literature for adverse event reporting
Strong analytic ability to analyze and summarize the main points of case reports, studies, and/or specific topics
Possesses experience with literature and safety databases
Problem-solving skills, especially with respect to enforcing safety rules and global procedures as described in SOPs, Operational Manuals, and Guidance Documents
Excellent written/oral communication skills are essential including fluency in English
Proactive behavior and ability to keep timelines in a fast-paced environment
Ability to develop cooperative working relationships with all levels of staff
Conversant in medical terminology; familiarity with MedDRA coding
Maintains comprehensive proficiency with Adobe Acrobat and Microsoft Office (e.g., Word, Excel, and PowerPoint) and associated modules
Possess a working knowledge and an understanding of global health authority regulations
Ability to work independently and as part of a team in a fast-paced environment.

#LI-Hybrid

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Refine Your Search

quality control associate jobs in county dublin

Senior Associate, Global Risk Management Programs

ERP Technical Delivery Manager

Senior Human Resources Associate

Associate Mechanical Engineer

Internal Audit Associate Director

Basic grade Cardiac Physiologist Permanent

Associate Director - Enterprise Risk Management

External Manufacturing Technical Lead – Large Molecule Drug Substance

Tax Risk & Controversy Senior Associate

Senior Process Engineer

Assistant Manager - Dundrum Town Centre, Hollister

Senior Associate - Fund Accounting

Director of Food & Beverage

Senior Process Engineer - Packaging

Key Lead - Dundrum Town Centre, Hollister

Asset & Wealth Management, Business Controls, Associate, Dublin

Global Financial Crimes Manager

Associate Director, Biostatistics

Senior Internal Auditor, Technology - Dublin or Amsterdam

Accountant FTC

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