Site Lead Auditor (Associate Director)

Msd Ireland

Carlow

Hybrid

EUR 90,000 - 120,000

Full time

16 hours ago

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Benefits offered by this job

Hybrid work model

Job summary

MSD Ireland in Carlow seeks a Site Lead Auditor to head the internal audit and inspection readiness programmes within a sterile fill-finish manufacturing facility. You will partner with functions to strengthen a compliant culture, ensure cGMP, and support reliable supply of medicines.

Responsibilities include delivering the site internal audit programme, leading inspection readiness, and communicating outcomes to stakeholders while driving CAPA and continuous improvement across the Quality

Qualifications

Bachelor’s degree or higher in a relevant scientific or engineering discipline.
Extensive GMP regulatory knowledge and auditing experience.
Proven ability to lead cross-functional audit programmes.
Strong analytical and problem-solving skills with stakeholder influence.

Responsibilities

Lead the site internal audit programme and risk-based oversight.
Direct the site inspection readiness programme and GMP inspections.
Provide Quality oversight for cGMP, contamination control, and regulatory compliance.
Develop and communicate audit metrics, CAPA tracking and effectiveness.
Engage with stakeholders to sustain a compliant culture and continuous improvement.

Skills

Audit Readiness

Audit Trails

Compliance Activities

Corrective Action Management

Decision Making

GMP

Manufacturing Audits

Metrics Development

Quality Improvement

Quality Management Systems

Quality Risk Management

Quality Standards

Regulatory Compliance

Regulatory Requirements

Education

Bachelor’s degree or higher in Chemistry, Biology, Microbiology, Engineering or another relevant discipline

Job description

Job Description

The Site Lead Auditor is a pivotal Quality leadership role within the companys quality organisation at the Carlow site, a sterile fill-finish manufacturing facility. You will lead the site internal audit and inspection readiness programmes, partnering across the organisation to build a strong, sustainable compliance culture. Through risk-based oversight, proactive regulatory intelligence and effective stakeholder engagement, you will help ensure cGMP compliance, patient safety and the reliable supply of medicines to our customers.

Key Responsibilities

Implementation and ongoing delivery of the site internal audit programme, aligned with site operational priorities.
Lead the site inspection readiness programme, embedding a culture of permanent inspection readiness.
Provide Quality oversight to ensure sterile fill-finish manufacturing processes comply with cGMP, contamination control expectations and applicable regulatory requirements.
Set clear compliance direction for the site by promoting adherence to divisional policies, guidelines and regulatory requirements.
Lead proactive assessment of site compliance against emerging regulations, industry expectations and regulatory trends.
Establish and maintain meaningful metrics for the site internal audit programme, ensuring timely communication, action tracking and follow-up.
Represent the site Quality Management System during Health Authority and internal GMP inspections.
Lead and perform facility, system and walkthrough audits, and manage the site internal audit schedule.
Maintain current technical, compliance, regulatory and auditing expertise to strengthen programme effectiveness and identify early compliance warning signals.
Communicate audit and inspection outcomes clearly to stakeholders and site leaders; critically assess root cause analyses and CAPA responses; monitor completion; and verify effectiveness to support sustainable remediation.
Support the preparation for and hosting of Health Authority inspections and divisional GMP audits.
Generate, analyse and report programme metrics and trends to demonstrate adherence, identify risk and drive ongoing effectiveness.

Bring energy, knowledge & innovation to carry out the following

The motivation and presence to be an inspiring contributor within a high-performing, collaborative team.
Strong communication, decision-making, influencing and project management skills.
Excellent problem-solving and critical-thinking capability, with the ability to connect technical and Quality System information and recognise potential compliance risks.
Knowledge, experience and leadership style to guide planning, strategy development and execution, supporting right-first-time performance and sustained compliance across the site’s sterile fill-finish operations.
A strong record of leadership and team contribution, with the judgement and accountability required for this highly responsible role.
Expert knowledge of cGMP and Quality System regulations relevant to the site.

Qualifications And Experience

Bachelor’s degree or higher in Chemistry, Biology, Microbiology, Engineering or another relevant discipline.
10+ years of experience in the pharmaceutical or biologics industry with a minimum of 4 years delivering site internal audit and inspection readiness programmes in a regulated environment.
Demonstrated GMP auditing experience within the pharmaceutical industry.
Proven ability to work cross-functionally, deliver against schedules and thrive in an interdependent work culture.
Strong organisational skills, with the ability to manage multiple priorities and exercise sound judgement on when to escape issues for resolution.

Our facility in Carlow site broke ground in 2008 and is a filling site for the launch and commercial supply of vaccines, biologics and small molecule drug product.Since its initial launch, the site has attracted significant internal investment and is now home to a number of state-of-the-art production facilities, laboratories and temperature-controlled warehousing units. The Carlow site is a significant employer in the South East region and attracts high performing talent through close collaborations with universities and colleges in the region

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 diverse, 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.

Required Skills

Audit Readiness, Audit Trails, Compliance Activities, Corrective Action Management, Decision Making, Good Manufacturing Practices (GMP), Manufacturing Audits, Metrics Development, Quality Improvement Programs, Quality Management Systems (QMS), Quality Risk Management, Quality Standards, Regulatory Compliance, Regulatory Requirements

Preferred Skills