Find Quality improvement specialist Jobs in County Mayo

Analytical Technology Specialist
AbbVie —Westport, County Mayo
- Full-time
- Management
- Master's degree
- Bachelor's degree
Stability Specialist
Vantive —Castlebar, County Mayo
- Doctoral degree
- Word processing
- Master's degree
Trade and Compliance Customs specialist
Vantive —Castlebar, County Mayo
- Microsoft Excel
- Analysis skills
Manufacturing Applications Developer & Database Specialist (EBR / MES)
Computeq —Castlebar, County Mayo
- €36,600–€55,156 a year
- Full-time
- Microsoft Access
- Oracle
- English
Quick apply
7d
Aseptic Specialist
AbbVie —Westport, County Mayo
- Full-time
- Engineering
- Manufacturing
- Communication skills
Manufacturing Specialist - 1st Shift
AbbVie —Westport, County Mayo
- Full-time
- Engineering
- Analysis skills
- Presentation skills
19h
Therapy Specialist, PD, Ireland
Vantive —Castlebar, County Mayo
- Nursing
- Clinic
- Leadership
Locum Consultant Physician in Geriatric Medicine
Woodston Personnel Ltd. —County Mayo
- On call
- Leadership
- Communication skills
- Teaching
Quick apply
6d
Maintenance Technician (Fitter) – Nights
AbbVie —Westport, County Mayo
- Overtime
- Maintenance
- Organisational skills
- Welding
Maintenance Fitter (Weekend Shift)
AbbVie —Westport, County Mayo
- Overtime
- Maintenance
- Welding
- Manufacturing
14d

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Stability Specialist
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Analytical Technology Specialist

AbbVie -
Westport, County Mayo

Apply Now

Job details

Full-time

Qualifications

Management
Procurement
Master's degree
Bachelor's degree
Technical writing
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

Job Summary:

Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline. Commercial drug product testing, ad-hoc investigation & development testing. Execute/assist on new method transfers and validations. Laboratory duties including critical reagent screening/qualifications, laboratory housekeeping, review of paperwork and procedural updates, support product release, drive completion of defined projects.

Key Responsibilities:

Completely follow established experimental protocols RFT and assess results
Recognize and report experimental variances
Learn, understand and effectively implement new experimental protocols and/or techniques
Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents
Perform routine tasks competently and independently generating reliable and consistent results
Analyse and critique results through assay performance monitoring and trending flagging issues and OFI with Management and Scientists
Demonstrate technical proficiency in their field, skill in multiple techniques and suggest protocol improvements within the Quality framework
Troubleshoot experiments and instrumentation, support Root Cause Analysis investigations, Impact projects through lab-based activities
Support team and work well with others, prepare solutions required for group testing
Enter laboratory results on Sample Management Systems
Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, GxP compliance and Data Integrity

Qualifications

Bachelor’s Degree, or equivalent education, with typically 12 months experience or Master’s Degree or equivalent education.
Bioassay/Cell culture/ELISA experience, theoretical and practical knowledge to carry out job function.
Ability to work independently with focus on Right First Time (RFT)
GXP Experience
Experience in procurement and/or shipping and/or sample management
Basic statistical knowledge is advantageous
Proven problem-solving ability
Clear communication skills and technical writing
Willingness to up-skill and collaborate
Ability to support priority projects to meet timelines

Additional Information

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

quality improvement specialist jobs in county mayo

Analytical Technology Specialist

Stability Specialist

Trade and Compliance Customs specialist

Manufacturing Applications Developer & Database Specialist (EBR / MES)

Aseptic Specialist

Manufacturing Specialist - 1st Shift

Therapy Specialist, PD, Ireland

Locum Consultant Physician in Geriatric Medicine

Maintenance Technician (Fitter) – Nights

Maintenance Fitter (Weekend Shift)

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