Prinova

Compliance

• Provide in depth review of regulatory matters for food, feed supplements activity in the EU, UK and outside the EU entities for Prinova Europe
• Provide training and troubleshooting
• Link with authorities, consultants and professional bodies on all regulatory matters
• Participate in company compliance initiatives
• Ensure regulatory compliance with food and feed safety, quality and defence as it relates to UK, EU and GFSI (BRC) requirements
• Monitor changes in legislation and regulatory requirements
• Support the development and implementation of regulatory strategies for existing and new ingredients/products in the UK and EU regions
• Provide regulatory review of product compliance
• Coordinate with authorities for all work required
• Support the design and maintenance of Prinova Specification
• Provide training for the quality and technical teams in Europe
• Actively support QA department tasks as required
• Provide support to the commercial and marketing team to verify regulatory compliance
• Assist in the management of crises and incidents

Regulatory Affairs Specialist

• Provide in depth review of regulatory matters for food, feed supplements activity in the EU, UK and outside the EU entities for Prinova Europe
• Provide training and troubleshooting
• Link with authorities, consultants and professional bodies on all regulatory matters
• Participate in company compliance initiatives
• Ensure regulatory compliance with food and feed safety, quality and defence as it relates to UK, EU and GFSI (BRC) requirements
• Monitor changes in legislation and regulatory requirements, proactively assessing the impact on business and updating the senior management team's compliance protocols as necessary
• Support the development and implementation of regulatory strategies for existing ingredients and new ingredients/products in the UK and EU regions ensuring compliance to but not limited to Allergens, REACH, Novel food, Packaging Food Contact Materials, Food Law and labelling, Feed laws and labelling, Residues and Contaminants, Natural and Botanical ingredients etc.
• Provide regulatory review of product compliance when an in-depth analysis/review is needed for the quality department
• Coordinate with authorities for all work required, such as authorisation and licenses
• Support the design and maintenance of Prinova Specification, ensure all information is correct and meets relevant EU regulation requirements
• Provide training for the quality and technical teams in Europe
• Actively support QA department tasks according to workload and priorities, as required
• Provide support to the commercial and marketing team to verify regulatory compliance
• Assisting, as required, in the management of crises and incidents as part of the management team

Software Engineer

• Complete customer product development & internal led innovation projects as assigned.
• Continuously build expertise on functional ingredients and nutrients - to be kept up to date on market trends.
• Be able to communicate professionally and effectively with our customers to assure robust scoping of all projects.
• Provide formulation and Nutrition support to all sections of the business and customers.
• Assure during the scoping process that our business truly understands the customer requirements and we can provide accurate indicative costs and approve/reject projects on this basis.
• Assure that in the scoping process we agree criteria in the scoping stage for product approval by the customer.
• Assure that all product development solutions are designed effectively to meet the customer requirements locked in the scoping stage which will include organoleptic, quality, legal & regulatory, stability and cost.
• Be able to design a product formulation from the customer idea whether that is a intermediate pre-mix, nutrition product (human or pet), RTD soft drink, or Dairy alternative product solution and implement it in the final manufacturing site (internal or external).
• Where applicable, complete sensory assessment prior to submission to the customer to assure that from an organoleptic perspective the products meet the agreed brief.
• Consider the role of the final packaging in the product shelf life based on industrial experience.
• Make informed decisions about the product shelf life based on the ingredient list, method of manufacture and final product packaging to be able to advise the customer as to an indicative product shelf life.
• Be able to advise customer on methodology to validate product shelf life.
• Assist in preparation and training provided to sales representatives and customers.
• Work alongside procurement and quality to identify and on board new raw material suppliers to meet customer needs as per the Prinova process. Ensure full approval is completed in a timely manner.
• Complete training for the broader team in product development.
• Scope and lead trials at our internal manufacturing facility and with third party manufacturers to support product development. (where required)
• Prepare for and attend first productions to assure that the manufacturing site is supported and any issues pertaining to the product can be dealt with effectively in a timely manner. (where required)
• Provide technical inputs for supplier raw material approval.

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Product Developer – Sports and Nutrition Supplements