Find Laboratory Jobs in County Mayo

Scientist I
AbbVie —Westport, County Mayo
- Full-time
- Writing skills
- Master's degree
- Bachelor's degree
Sample Pull QA Technician ( 12 month FTC)
AbbVie —Westport, County Mayo
- Full-time
- Microsoft Word
- Word processing
- No degree
QC Analyst - 12 month FTC
AbbVie —Westport, County Mayo
- Full-time
- Analysis skills
- Communication skills
- Time management
1h
Scientist II
AbbVie —Westport, County Mayo
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Downstream Process Scientist
Vantive —Castlebar, County Mayo
- Master's degree
- Bachelor's degree
- Organisational skills
7d
Analytical Technology Specialist
AbbVie —Westport, County Mayo
- Full-time
- Management
- Master's degree
- Bachelor's degree
Quality Operational Excellence Engineer
Vantive —Castlebar, County Mayo
- Engineering
- Analysis skills
- Bachelor's degree
Senior Supplier Quality Engineer (Temp)
Hollister ULC —Ballina, County Mayo
- Engineering
- ERP systems
- Microsoft Office

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Sample Pull QA Technician ( 12 month FTC)
AbbVie —Westport, County Mayo
Computer skills proficiency including word processing, spreadsheets, instrumentation related and AbbVie network systems.

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Scientist I

AbbVie -
Westport, County Mayo

Apply Now

Job details

Full-time

Qualifications

Writing skills
Master's degree
Bachelor's degree
Communication skills

Full job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Fixed-Term Contract | 1 Year

About the Role

We are currently seeking a Scientist I to join our talented and ambitious analytical team on a 1-year fixed term contract. This is an exciting opportunity to contribute to a collaborative, science-led environment where you will support routine analytical testing and play a key role in the development, validation, and continuous improvement of analytical methods.

In this role, you will perform routine testing using ELISA, HPLC, Karl Fischer, and other compendial methods while contributing to the delivery of high-quality data in support of project and operational needs.

Key Responsibilities

Perform routine testing using ELISA, HPLC, Karl Fischer, and other compendial analytical methods.
Participate in the development, optimization, and validation of analytical methods in line with project requirements, regulatory standards, and company procedures.
Accurately document, review, and interpret experimental results and observations.
Troubleshoot and resolve technical issues related to analytical instrumentation and methodologies.
Maintain laboratory equipment, manage reagents and consumables, and help ensure a safe and well-organized laboratory environment.
Collaborate effectively with team members to support efficient workflow and timely project completion.
Communicate clearly and professionally with colleagues and management regarding project status, results, and any technical issues.
Understand and adhere to corporate standards, including Good Manufacturing Practice (GMP), code of conduct, safety requirements, and appropriate handling of materials such as controlled drug compounds, as applicable.

Qualifications

Required

Bachelor’s degree, or equivalent education, with typically 3 years of relevant experience; or
Master’s degree, or equivalent education, with typically 1 year of relevant experience.

Required Skills and Experience

Demonstrated ability to perform quantitative ELISA assays.
Demonstrated ability to perform HPLC and/or compendial assays.
Ability to learn, understand, and master new experimental techniques.
Strong ability to multitask and work to timelines.
Demonstrated scientific writing skills.
Strong verbal communication skills.

Additional Information

We are looking for someone who is proactive, collaborative, and eager to contribute to a high-performing analytical team. The ideal candidate will be comfortable working in a regulated laboratory environment and motivated to deliver quality results.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Apply Now

Refine Your Search

laboratory jobs in county mayo

Scientist I

Sample Pull QA Technician ( 12 month FTC)

QC Analyst - 12 month FTC

Scientist II

Downstream Process Scientist

Analytical Technology Specialist

Quality Operational Excellence Engineer

Senior Supplier Quality Engineer (Temp)

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