Key Skills
Job Description
About the role
Are you passionate about quality, compliance and continuous improvement? At Niacet, a Kerry Company, we are looking for a QA Specialist to play a key role in maintaining and enhancing our Quality Management Systems within a dynamic manufacturing environment serving the food and pharmaceutical industries.
The QA Specialist is responsible for the maintenance, continuous improvement and day-to-day execution of site quality systems and controlled documentation processes. The role supports certification compliance, audit readiness, customer documentation requests and the effective follow-up of quality system activities within an international manufacturing environment, ensuring the highest standards of quality, safety and compliance are consistently achieved.Located in Niacet B.V, Tiel and reporting to the Quality Manager.
As a QA Specialist, you will support the effective management of quality systems, controlled documentation, certification requirements and customer quality requests. Working closely with teams across Quality, QC, Production, ESHQ, Sales and Customer Service, you will help ensure our processes remain compliant, audit-ready and aligned with both customer expectations and regulatory standards.
This is an excellent opportunity for a detail-oriented professional who enjoys collaborating across departments, driving quality excellence and contributing to the production of products that support both food safety and healthcare worldwide.
About Kerry
Kerry is the world's leading taste and nutrition partner for the food, beverage, and pharmaceutical industries. Every day, we work behind the scenes with our customers to solve some of the world's most complex food challenges through our wide range of ingredients, technologies, and expertise. We do everything with passion and continuously innovate to create a future of healthier, tastier, and more sustainable food without compromise. Our ambition is to be our customers' most valued partner, create a world of sustainable nutrition, and reach more than two billion consumers with sustainable nutrition solutions by 2030.
Niacet, a Kerry company, produces organic salts that are primarily used in the food industry and in the manufacture of various medicines. Our organic salts are used, for example, to extend the shelf life of bread and meat, protect against bacteria such as salmonella, and enhance flavour. In addition, our organic salts are used by the world's largest producers of insulin and kidney dialysis fluids. As a result, our products play an important role not only in healthy nutrition but also in healthcare.
Niacet places great importance on the wellbeing of its employees and is also committed to making a positive contribution to the local community. By sponsoring a variety of activities in Tiel related to sports and culture, Niacet strives to support and strengthen the community in a meaningful way.
What will you be doing?
- Maintain and continuously improve the site Quality Management System, including procedures, work instructions, forms, records and supporting quality documentation.
- Support compliance with applicable food, feed and pharmaceutical quality standards and regulations, including FSSC 22000, GMP+, ISO 9001, GMP and relevant FDA requirements.
- Coordinate document control activities, including the creation, review, approval, revision, periodic review and archiving of controlled documents.
- Manage and respond to customer quality documentation requests, questionnaires, declarations, certificates, specifications and other quality-related information.
- Support the preparation, execution and follow-up of internal, customer, supplier, certification and regulatory audits.
- Coordinate and support quality system processes, including deviations, non-conformances, CAPA, change control, risk assessments and effectiveness reviews.
- Collect, review and maintain quality records and supporting evidence to ensure ongoing audit readiness, certification compliance and customer assurance.
- Support supplier and external service provider quality documentation activities, including quality agreements, certifications and questionnaires.
- Prepare quality reports, KPI inputs, trend analyses and management review data to support informed decision-making and continuous improvement.
- Assist in the delivery of training related to quality systems, GMP awareness, documentation requirements and certification standards.
- Monitor updates to relevant regulations, standards, customer requirements and internal procedures, supporting their implementation within the Quality Management System.
- Collaborate closely with Quality Control, Production, ESHQ, Sales, Customer Service and other stakeholders to ensure effective communication, timely responses and successful delivery of quality system priorities and customer requirements.
- Identify opportunities for process improvement and support initiatives that enhance quality performance, compliance and operational efficiency.
What do you need to be successful?
- Experience in Quality Assurance, quality systems or document control within a regulated manufacturing environment.
- Experience in the food, feed, pharmaceutical, chemical or ingredients industry is preferred.
- Knowledge of quality standards such as FSSC 22000, GMP+, ISO 9001 and GMP.
- Experience supporting audits, CAPA, change control, deviations and non-conformance processes.
- Strong organisational skills with a structured and detail-oriented approach.
- Excellent communication skills in Dutch and English.
- Ability to work effectively with cross-functional teams and external stakeholders.
- HBO+ level or degree in Food Science, Chemistry, Pharmaceutical Sciences, Quality Management or a related discipline.
- Proficient in managing quality documentation, reports and compliance records.
Core Responsibilities
The QA Specialist is responsible for maintaining and improving site quality systems, controlled documentation, and ensuring compliance with food and pharmaceutical regulations. They will coordinate audit readiness, manage customer quality requests, and collaborate across departments to drive quality excellence.
Requirements
Candidates should have experience in quality assurance or document control within a regulated manufacturing environment, preferably in the food or pharmaceutical industry. An HBO+ level degree in a relevant scientific or quality management discipline is required, along with proficiency in quality standards like ISO 9001 and GMP.
About Kerry Group
Industry: Food and Beverage Services
Company size: 10,001+ employees
Every day, millions of people across the world consume foods and beverages containing our taste and nutrition solutions. Our portfolio spans food, beverage, biotechnology, pharma, and proactive health. We are committed to making the world of food and beverage better for everyone, and dedicated to our Purpose, Inspiring Food, Nourishing Life. We are a company rich in heritage and resources. Over the past five decades, our focus on changing lifestyles, the globalisation of food tastes and ever-evolving consumer needs has brought us to a market-leading global position. Today, we are firmly established as a world leader in the food, beverage and pharma industries, with 19,000+ staff, 119 manufacturing facilities, and 60+ technology and innovation centres globally. We are proud to provide our customers – some of the world’s best-known food, beverage and pharma brands – with the expertise, insights and know-how they need to deliver products that people enjoy and feel better about consuming. Learn more about us on www.kerry.com