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Project Manager (Construction)

Lead Group Ireland
Cork, County Cork

Quick apply

Job details

Permanent | Full-time
6 hours ago

Benefits

Company car

Qualifications

Engineering
Quality management
Microsoft Office
Project management
Bachelor's degree
Organisational skills
Quality systems
Document management systems
Leadership
Communication skills

Full job description

We are seeking a motivated and detail-oriented Quality Engineer to join our team in Cork. This site-based role is located within a large GMP-regulated manufacturing facility and is ideally suited to a quality professional with around 2 years of experience supporting validation activities, protocol execution, and quality documentation within the pharmaceutical, biotechnology, medical device, or broader life sciences sector

The successful candidate will play a key role in ensuring compliance with quality and regulatory requirements, supporting validation programmes, and driving continuous improvement initiatives across manufacturing and quality operation

Key Responsibilities

Support the development, execution, review, and approval of validation and qualification documentation, including IQ, OQ, PQ, and associated protocols and reports.
Ensure validation activities are completed in accordance with GMP requirements, site procedures, and regulatory expectations.
Assist with the management and maintenance of quality documentation, including change controls, deviations, CAPAs, and risk assessments.
Participate in root cause investigations and support the implementation of effective corrective and preventive actions.
Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, Quality Assurance, and Regulatory Affairs to maintain compliance and product quality.
Support equipment and process validation activities as required.
Assist with internal and external audits and ensure timely resolution of audit observations.
Contribute to quality metrics, continuous improvement projects, and operational excellence initiatives.

Requirements

Bachelor's degree in Engineering, Life Sciences, Quality, or a related discipline.
Minimum of 2 years' experience in a Quality, Validation, or Compliance role within a GMP-regulated pharmaceutical, biotechnology, medical device, or life sciences environment.
Practical experience working with validation protocols, qualification documentation, and GMP documentation practices.
Strong understanding of GMP requirements and quality systems.
Experience supporting investigations, deviations, CAPAs, and change control processes.
Excellent attention to detail, documentation, communication, and organisational skills.
Ability to work effectively within a cross-functional team environment.

Desirable Experience

Experience supporting equipment or process validation activities.
Familiarity with risk management methodologies and validation lifecycle principles.
Knowledge of electronic quality management systems (eQMS) and document management systems.
Experience participating in audits and regulatory inspections.

Benefits:

Company car

Work Location: In person

Quick apply

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