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At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join us in our mission to use the power of leading-edge science to save and improve lives around the world.
Responsibilities
- Participate as a functional expert in the cross-functional team responsible for introducing products and materials at Carlow.
- Review documentation associated with new product and material introduction, such as Material Packs, QC Test Specifications, BOMs, Supplier Qualification and Oversight.
- Develop and monitor supplier performance metrics, participate in material review boards and quarterly reviews of key suppliers, and actively engage in cross-functional forums as needed.
- Maintain the approved supplier management list within the qualified Supplier Management system, ensuring correct setup of suppliers and materials used at Carlow.
Qualifications
- Currently pursuing a relevant degree qualification.
- Knowledge of regulatory/code requirements related to Irish, European, and International Codes, Standards, and Practices.
- Strong report, standards, and policy writing skills.
- Proficiency in Microsoft Office and job-related computer applications.
- Good collaboration skills and the ability to work effectively as part of a team to determine priorities.
- Demonstrated ability to work independently and take ownership of improvement initiatives with a moderate level of guidance.
- Proven ability to drive the completion of tasks.
- Strong decision-making capability with a sense of accountability and responsibility.
- Demonstrated problem-solving skills.
Required Skills
Analytical Problem Solving, Clinical Research, Data Analytics, Database Management, Data Entry, Data Visualization, Decision Making, Document Management, Financial Acumen, Health Economics, Microsoft Applications, Office Applications, Office Management, Problem Identification, Process Improvements, Project Management, Reporting and Analysis, Results-Oriented, Retention Strategies, Review Meetings, Standards Development, Supplier Auditing, Taking Initiative, Task Management.
Employee Status
Intern/Co-op (Fixed Term)
Relocation
No relocation
VISA Sponsorship
No
Travel Requirements
No Travel Required
Flexible Work Arrangements
Hybrid
Shift
Not Indicated
Valid Driving License
No
Hazardous Material(s)
N/A
Job Posting End Date
09/16/2026
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Sectors
Locations
Sectors
Locations
At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join us in our mission to use the power of leading-edge science to save and improve lives around the world.
Responsibilities
- Participate as a functional expert in the cross-functional team responsible for introducing products and materials at Carlow.
- Review documentation associated with new product and material introduction, such as Material Packs, QC Test Specifications, BOMs, Supplier Qualification and Oversight.
- Develop and monitor supplier performance metrics, participate in material review boards and quarterly reviews of key suppliers, and actively engage in cross-functional forums as needed.
- Maintain the approved supplier management list within the qualified Supplier Management system, ensuring correct setup of suppliers and materials used at Carlow.
Qualifications
- Currently pursuing a relevant degree qualification.
- Knowledge of regulatory/code requirements related to Irish, European, and International Codes, Standards, and Practices.
- Strong report, standards, and policy writing skills.
- Proficiency in Microsoft Office and job-related computer applications.
- Good collaboration skills and the ability to work effectively as part of a team to determine priorities.
- Demonstrated ability to work independently and take ownership of improvement initiatives with a moderate level of guidance.
- Proven ability to drive the completion of tasks.
- Strong decision-making capability with a sense of accountability and responsibility.
- Demonstrated problem-solving skills.
Required Skills
Analytical Problem Solving, Clinical Research, Data Analytics, Database Management, Data Entry, Data Visualization, Decision Making, Document Management, Financial Acumen, Health Economics, Microsoft Applications, Office Applications, Office Management, Problem Identification, Process Improvements, Project Management, Reporting and Analysis, Results-Oriented, Retention Strategies, Review Meetings, Standards Development, Supplier Auditing, Taking Initiative, Task Management.
Employee Status
Intern/Co-op (Fixed Term)
Relocation
No relocation
VISA Sponsorship
No
Travel Requirements
No Travel Required
Flexible Work Arrangements
Hybrid
Shift
Not Indicated
Valid Driving License
No
Hazardous Material(s)
N/A
Job Posting End Date
09/16/2026
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
