23h ago
New

Senior Specialist, Quality

Irl - Louth County - Dundalksenior
Manufacturing & ProductionQuality Manager
0 views0 saves0 applied

Quick Summary

Overview

Job Description About the Role and Site Join a state-of-the-art vaccines manufacturing facility in Dundalk and play a critical role in ensuring the highest standards of quality, compliance,

Technical Tools
Manufacturing & ProductionQuality Manager

About the Role

~1 min read

Join a state-of-the-art vaccines manufacturing facility in Dundalk and play a critical role in ensuring the highest standards of quality, compliance, and operational excellence across both Drug Substance and Drug Product manufacturing operations.


As a Senior Specialist within Quality Assurance Operations, you will provide independent quality oversight, partnering closely with Manufacturing, Quality Control, Engineering, Technical Operations, Supply Chain, and Quality Systems teams. This highly visible role supports commercial manufacturing, technology transfer, investigations, and continuous improvement activities while helping to maintain a culture of quality and inspection readiness.


This is an excellent opportunity for a quality professional looking to broaden their impact in a fast-paced manufacturing environment while working across multiple operational functions.



  • Provide quality oversight and support for Drug Substance and Drug Product manufacturing operations.
  • Review and approve GMP documentation, batch records, protocols, reports, and manufacturing records.
  • Support batch disposition activities and quality decision-making processes.
  • Lead and support investigations, deviations, corrective and preventive actions, change controls, and risk assessments.
  • Partner with manufacturing and technical teams to support technology transfer, process validation, and commercial manufacturing activities.
  • Drive inspection readiness and support internal audits and regulatory inspections.
  • Monitor quality performance metrics, identify trends, and implement continuous improvement initiatives.
  • Provide GMP guidance and quality expertise across manufacturing and support functions.
  • Support site and global quality projects, change initiatives, and compliance programmes.
  • Champion a culture of quality, compliance, accountability, and operational excellence.


Required

  • Bachelor’s degree in a scientific or engineering field (such as Biotechnology, Microbiology, Pharmacy, or a related Life Sciences discipline).
  • Minimum of 5 years of relevant experience in a regulated Good Manufacturing Practice (GMP) environment, such as pharmaceutical, biotechnology, or biologics manufacturing.
  • In-depth knowledge of GMP requirements, Quality Systems (e.g., deviations, CAPA, change control), and global regulatory expectations.
  • Proven ability to lead and support quality activities, including investigations, batch disposition, and inspection readiness programmes.

Preferred

  • Strong collaborative and influencing skills, with the ability to partner effectively with cross-functional teams and stakeholders.
  • Proven experience with Quality Management Systems, including participation in the implementation and deployment of QMS.
  • Demonstrated leadership capabilities with excellent problem-solving, risk-based decision-making, and oral and written communication skills.
  • Experience supporting technology transfers, process validation, and continuous improvement initiatives.
  • Expertise in bioprocessing, aseptic manufacturing, or commercial manufacturing support.
  • Passion for fostering a culture of quality, compliance, and operational excellence.

Additional location(s) Compensation Information:

cGMP Regulations, Change Management, Deviation Management, Pharmaceutical Quality Assurance, Quality Management Standards, Quality Standards, Risk Management, Strategic Planning

Nice to Have

~1 min read

Current Employees apply HERE

Current Contingent Workers apply HERE

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs. 


As an equal opportunity employer, we are proud to be a company that embraces the value of bringing inclusive, talented, and committed people together. 


Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process. 


We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world. 


Please feel free to speak to us about what flexibility means to you during your application. 


Invent solutions to meet unmet healthcare needs, please apply today

Regular

No relocation

No

Requirements

~1 min read
No Travel Required

Not Applicable

Not Indicated

No

N/A

11/7/2026

Location & Eligibility

Where is the job
Irl - Louth County - Dundalk
On-site at the office
Who can apply
Same as job location

About this job

Posted
Today
Employer
has 2,170 open jobs on Jobera in 4 countries.

Listing Details

Posted
October 27, 2026
First seen
October 27, 2026
Last seen
October 27, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
51%
Scored at
October 27, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust
Newsletter

Stay ahead of the market

Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.

A
B
C
D
Join 12,000+ marketers

No spam. Unsubscribe at any time.

Senior Specialist, Quality