Vaccine Manufacturing Site Leader

About Phibro Animal Health Corporation

This globally operating organization is built on a rich history of animal health and nutrition. We offer medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition that cater to the needs of livestock producers, farmers, veterinarians, and consumers. Our vision is to be a trusted partner in helping them maintain and enhance the health of their animals.

We strive to achieve operational excellence by fostering a culture of collaboration and continuous improvement. This drives us to innovate and develop solutions for various markets. As a diversified company, we operate in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for different industries.

Our workforce is our greatest asset, comprising over 2,300 employees worldwide who are dedicated to providing top-notch solutions. At Phibro, we aim to develop a diverse team that fosters an environment where individuals feel supported in sharing their creativity and skills. This enables them to grow professionally and reach their full potential.

We welcome applicants from diverse backgrounds who may not meet all qualifications but believe they can contribute to our success. If you're interested in joining our team, we encourage you to apply.

The Site Director plays a pivotal role in our Management team based out of Sligo, Ireland. This key position oversees the operation, governance, and strategic development of the vaccine manufacturing site.

Leadership and Management:

Provide effective leadership and direction to the manufacturing site, encompassing production, quality, engineering, EHS, technical services, supply chain, and site administration. Foster a culture of excellence, collaboration, and continuous improvement.

Health and Safety:

Ensure a safe working environment for all employees by implementing and maintaining health and safety policies and procedures.

Operational Oversight:

Guarantee the smooth and efficient operation of all manufacturing processes, including production, quality control, and maintenance.

Regulatory Compliance:

Ensure the site maintains full compliance with HPRA, EMA, and other relevant global regulatory standards. Serve as the senior point of contact for regulatory inspections and audits.

Quality Assurance:

Oversight the implementation and adherence to quality assurance programs, ensuring the highest standards of product quality and safety.

Operational Excellence:

Drive continuous improvement, lean manufacturing initiatives, and operational efficiency to achieve safety, quality, cost, and delivery targets.

Stakeholder Engagement:

Liaise with internal and external stakeholders, reporting KPIs and metrics to corporate stakeholders.

Strategic Planning:

Develop and implement long-term strategic plans for site expansion, capability development, and new product introductions.

Talent Development:

Lead, mentor, and develop a high-performing leadership team and workforce. Champion a strong safety and quality culture.

Financial Management:

Develop and manage the site budget, ensuring cost-effective operations and adherence to financial targets.

Risk Management:

Identify and mitigate risks related to business continuity, compliance, and supply chain disruptions.

Education:

Masters Degree (Level 9 Irish National Framework of Qualifications) in a relevant field such as Pharmaceutical Science, Biotechnology, or Engineering.

Experience:

Minimum 15 years of experience in a manufacturing environment, with at least 5 years in a senior leadership role within the pharmaceutical or biotechnology industry.

A proven track record of managing large teams and complex operations.

In-depth knowledge of EU GMP and other relevant standards.

Strong financial acumen and experience with budget management.

Excellent knowledge of the Irish regulatory environment – GMP, EHS, Legal, Corporate Governance, Financial, Customs.

Excellent leadership, communication, and stakeholder management skills.

Demonstrated understanding of GMP, aseptic processing, cold chain logistics, and biologics manufacturing technologies.

Ability to develop and implement strategic plans and drive organizational change.

Strong problem-solving and decision-making abilities.

Experience working in a matrixed, multinational environment.

Track record of fostering a high-performance and quality-focused culture.

We offer a competitive benefits package designed to support the well-being of our employees and their families. For more information, please visit our website.

We are an Equal Opportunity Employer committed to diversity and inclusion. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status, or any other protected characteristics.

Ireland - Sligo

Monday - Friday (40 hours)