Regulatory Specialist

3 weeks ago


Liverpool, United Kingdom Avient Full time

**The Role**

**Accountabilities**
- Europe
- USA (FDA)
- Asia
- Mercosur
- Classification and labelling
- REACh
- BPD
- Global chemical inventories
- Overseeing document generation for customers:

- MSDS
- Declarations of compliance with food contact legislation, heavy metals legislation, absence of specific hazardous chemicals.
- Dealing with non-routine complex customer enquiries, customer questionnaires, migration data requests, legislative explanations. Escalating issues to Regulatory Manager as required in a timely manner and seeking assistance if required.
- Reviewing the impact on finished goods compliance status when there are changes in the status of raw materials, coordinating discussions with relevant parties to collectively decide an appropriate path forward (e.g. reformulation, communicate change to customers etc.).
- Reviewing new chemistry types for compliance with the legislations listed above.
- Supporting REACH registration of chemicals and development of strategies for REACH registration (i.e. cost/benefit analysis and data gap analysis).
- Provide project support as required related to data management for existing materials (i.e. migration data collation, toxicological data collation).
- Provide project support as required to support the business in adhering to new chemicals legislation (i.e. GHS, new chemical inventory notification requirements).
- Providing adequate regulatory support and resource to selected strategic business projects delegated by Regulatory Manager, including collation of technical and regulatory data to support business activities as required.
- Reviewing and approving COSHH assessments. Supporting Regulatory Coordinator with COSHH assessments for any new trial materials.
- Act as main point of contact with brand owners for new product approvals, manage approvals processes, responding to queries and following up as necessary.

**Responsibilities**
- Assisting in addressing legislative developments and supporting the Regulatory Manager as required.
- Liaising with third party laboratories to coordinate purity testing and migration studies and other evaluations as needed.
- Compiling technical reports for both internal and external use related to:

- Technical effects of materials
- Regulatory status (Chemical inventories and Food Contact)
- Migration from polymer substrates
- Toxicological and exposure data
- Purity data
- Managing data in SAP EHS module and supporting regulatory coordinator with generation of MSDS’.
- Managing communications with internal and external customers regarding the regulatory status of finished products.
- Producing documentation as required answering customer enquiries.
- Other duties as assigned or needed.

**Competencies, Qualification & Experience Required**

Competencies

Customer Focus

Action Orientated

Instills Trust

Demonstrates Self Awareness

Collaborates

Communicates Effectively

Being Resilient

Situational Adaptability

Qualifications & Experience Required
- Degree in a scientific discipline, with a strong background in Food Contact legislation (EU PIM 10/2011, FDA 21 CFR).
- Knowledge of GHS and classification and labelling would also be an advantage.
- A good understanding of analytical chemistry techniques and also a basic understanding of key toxicological principles is also required.
- Previous experience where effective multi-tasking is required.



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