Find senior product qa Jobs in sligo, so

Specialist, QA Compliance
AbbVie —Sligo, County Sligo
- Full-time
- Hybrid work
- Engineering
- Communication skills
Senior Product QA Manager
AbbVie —Sligo, County Sligo
- Full-time
- Master's degree
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- Communication skills
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AbbVie —Sligo, County Sligo
- Full-time
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Manager, Quality Control
AbbVie —Sligo, County Sligo
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
Quality Assurance Manager - Medical Devices
AbbVie —Sligo, County Sligo
- Full-time
- Hybrid work
- Engineering
- Master's degree
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Specialist, QA Compliance

AbbVie -
Sligo, County Sligo

Apply Now

Job details

Full-time

Qualifications

Engineering
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

In AbbVie Ballytivnan, we are recruiting for a QA Compliance Specialist to join our team. This position will report into the Quality Systems Manager. The QA Compliance Specialist is responsible for documenting and establishing a quality system which ensures full compliance with all regulatory and AbbVie requirements.

The QA Compliance Specialist will have responsibility to assess and report on the effectiveness of the quality system to senior management.

What you will do:

Coordinating the quality system, ensuring full compliance by all personnel with its requirements.
Coordination of Product Quality Reviews activities.
Management of all Technical Agreements from initiation, review, approval and storage.
Coordination and Management of all Track and Trend activities to support Manufacturing and QC. Driving a QRM approach to all activities on site.
Coordination and facilitation of all Site RCS and FMEA activities.
Auditing the quality system per the documented internal audit schedule.
Assisting in the documentation, investigation of and coordinating customer complaints/exceptions by ensuring implementation of effective corrective / preventive action where necessary.
Ensuring that products manufactured at Abbvie Biologics Ballytivnan meet requirements of end users, of regulatory authorities and of the company.
Measuring performance of the quality system and reporting on this at the management review meeting and during quality performance meetings.
Coordinating change management, change control and Change planning activities. Monitoring quality performance and advising management personnel on major quality issues.
Liaison with AbbVie Global Quality Assurance, FDA, HPRA and other regulatory bodies. Regulatory review.
Initiation and Completion of Quality related investigations and verification of the effectiveness of CAPA’s as required.
Establishing Corrective / Preventive Action system and procedures.
Management of the Supplier program including the ASL, Performance metrics and Audit Schedules.
Creation and approval of commodity specifications as required.
Performance of Vendor audits as required Supporting all aspects of inspection readiness including preparation activities, logistic activities, and generation of follow up responses and management of proof books.

Qualifications

What you will need:

A third level qualification in a science, quality or engineering discipline
Minimum 3 years’ Experience in a similar role in a Pharmaceutical or Sterile Manufacturing environment
A strong knowledge of regulatory requirements is required.
Excellent written and verbal communication skills with a strong attention to detail.

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

senior product qa jobs in sligo, so

Specialist, QA Compliance

Senior Product QA Manager

Senior NPI Compliance Specialist

Manager, Quality Control

Quality Assurance Manager - Medical Devices

Head of Engineering

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