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Quality Assurance Specialist (12 Month Fixed Term Contract)

Almac Group -
Dundalk, County Louth

Apply Now

Job details

Full-time
From €40,000 a year
6 days ago

Qualifications

Manufacturing

Full job description

Location: Dundalk

Hours: 37.5 Hours

Salary: Competitive

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB11707

*Please note that if you have alreday applied for this position in the past 12 months, you do not need to repply as your exisiting application will remain valid*

The Role

The Quality Assurance Specialist will play a crucial role in assessing and enhancing the Quality System to ensure Good Manufacturing Practice (GMP) compliance and the quality of pharmaceutical products. They will provide quality assurance support and advice to various operational departments, interacting with both internal and external customers to meet project timelines while maintaining high standards of product quality and compliance.

Key responsibilities include assisting in the implementation and continuous improvement of quality systems such as deviation and CAPA management, change controls, and risk assessments. The post holder will also serve as a point of contact for queries related to product compliance and quality.

Additionally, the post holder will be involved in monitoring and reviewing quality system elements, such as deviation reports, corrective and preventative actions, change controls, complaints, audits, and out-of-specification reports. They will review data related to secondary packaging activities and validation reports to ensure accuracy and compliance.

Key Requirements

Have eligibility to work in IE OR possess a valid work permit that will allow you to take up full time employment in IE
Degree (or equivalent) in a Life Science or closely related field
Minimum 3 years EU GMP experience working in a Quality role within the Pharmaceutical Industry
Comprehensive, working knowledge of the regulatory requirements for pharmaceutical products are essential, including familiarity with the principles of Good Manufacturing Practice, Pharmaceutical Quality Systems, Quality Risk Management and Pharmaceutical Product Lifecycles
Experience with New Product Introduction and/or experience in a client facing role is highly desirable

Further Information

The working pattern for this role is a flex pattern between the hours of 07:00 19:00 with core hours of 10:00 16:00.

You will also be eligible for hybrid working following the successful completion of probation. This role requires coverage beyond normal working hours on a regular basis and it is a condition of your employment that you are able to fulfil this requirement of the role.

Apply Now

Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.

Closing Date

We will no longer be accepting applications after 5pm on 30th July 2026.

RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.

Apply Now

Refine Your Search

secondary project jobs

Quality Assurance Specialist (12 Month Fixed Term Contract)

Mechanical Stress Engineer

Project Quantity Surveyor:Buildings

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Clinical Nurse Specialist Radiation Oncology - Limerick Cancer Centre

Principal Engineer - Data Centres (HV Substation Design) - ROI

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