CPL

IT Application Support

View CPL profile
Location
Tipperary, Co. Tipperary
Location type
At the office
Employment type
Full time
Job type
Permanent
Salary
Negotiable
Apply now
Apply now

Key Responsibilities
1. Application Support & Maintenance
o Monitor and maintain pharmaceutical applications to ensure optimal
performance and availability.
o Perform regular system health checks and proactive maintenance.
o Apply patches, updates, and upgrades to applications as needed.
2. Hardware and Software Maintenance:
o Install, configure, and maintain computer systems, printers, and other peripherals.
3. Help Desk Support:
o Respond to user inquiries and provide technical support via phone, email, or inperson.
o Troubleshoot application errors and work with development teams to
implement fixes.
o Diagnose and resolve hardware, software, and network issues promptly.
o Provide timely and clear communication to end-users regarding the status of their
requests.
o Log and track support requests using a ticketing system.
o Document incidents, problems, and resolutions for future reference.
4. System Administration:
o Administer and maintain enterprise-level systems and applications.
o Implement and manage Active Directory, user accounts, and group policies.
o Perform regular system backups and ensure disaster recovery procedures are in
place.
o Support with provision and review where applicable of Audit Trails for system
owners to review.
5. User Assistance & Training
o Provide technical support and training to end-users on application
functionalities and best practices.
o Develop user guides, training materials, and documentation to assist users.
6. Collaboration & Communication
o Work closely with cross-functional teams including IT, development, QA, and
vendors to resolve application issues.
o Communicate effectively with stakeholders to keep them informed of issue
status and resolutions.
7. Compliance & Security
o Ensure applications comply with regulatory requirements and industry
standards (e.g., FDA, GMP, SOX).
o Implement and maintain security protocols to protect sensitive data.
8. Performance Optimization
o Analyze application performance and implement improvements to enhance
efficiency and user experience.
o Conduct regular reviews and assessments to identify areas for optimization.
9. Project Involvement
o Participate in application-related projects, including new implementations,
upgrades, and migrations.
o Assist in requirement gathering, testing, and deployment phases.
10. Electronic System Implementation:
o Project Manage the delivery of electronic systems, inc requirements gathering,
scheduling, budgeting.
o Develop and execute validation protocols (IQ, OQ, PQ) for GxP systems to ensure
compliance with regulatory requirements.
11. Reporting & Documentation
o Generate and analyze reports on application performance and usage.
o Maintain detailed and accurate documentation of support activities,
configurations, and processes.
12. Audit Support:
a) Prepare for and participate in regulatory inspections and audits.
b) Address findings and implement corrective and preventive actions (CAPAs) as
needed.
Qualifications
• Education: Bachelor’s degree in Computer Science, Information Technology, or related
field.
• Experience:
o Minimum of 3-5 years of experience in application support, preferably in the
pharmaceutical or healthcare industry.
o Experience with pharmaceutical applications such as LIMS, ERP, CRM, or
specific pharma software.
• Technical Skills:
o Proficiency in SQL, database management, and scripting languages.
o Familiarity with application servers, web servers, and middleware technologies.
o Knowledge of pharmaceutical regulatory requirements and validation
processes.
• Soft Skills:
o Strong problem-solving and analytical skills.
o Excellent communication and interpersonal skills.
o Ability to work independently and as part of a team.
• Certifications (Preferred): ITIL, CompTIA A+, or other relevant certifications.

#LI-VH2

Important Dates
Posted on
03 July, 2024
Reference number
JO-2407-537300

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