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Blue Pebbles

Quality & Regulatory Coordinator (Pharma/Food)

Vacancy Title: Quality & Regulatory Coordinator (Pharma/Food)
Contract Type: Permanent
Location: Leicester
Industry:
Salary: Competitve starting salary
Start Date: 2024-01-30
REF: J923557
Contact Name: Hannah Williams
Contact Email: Hannah.Williams@russell-taylor.co.uk
Vacancy Published: about 1 month ago

Vacancy Description

Role: -Quality & Regulatory Coordinator (Pharma/Food)
Salary: - Competitive starting salary
Location: -Leicestershire

Russell Taylor Group have a fantastic opportunity for an individual with a couple of years' experience within the Quality and Regulatory field to join Supplement SME Manufacturer in the Leicestershire area.
For this role, our client is looking for someone who is ready to roll their sleeves' up and get stuck straight into the role and is willing to be ready for a challenge. This role is within the Quality and Regulatory team, so does require experience within these functions, ideally within a GMP or HACCP regulated environment. It is a small team, so you have lots of exposure and learning development opportunities.
Our client is looking to move fast with this position and will be looking to interview asap, so if you are interested, please apply within.

Responsibilities
• Ensure that the company meets regulatory and quality assurance guidance and legislation for Food Law and medicinal products.
• Maintain the quality management system
• Registration of products for export markets.
• Involved in the registration of organic, vegan, and kosher products.
• Update and maintain product specifications
• Approve raw material specifications
• Be involved in the approval of suppliers
• Be involved in implementing Forms, SOPs, and Appendices into the quality management system.
• Review SOPS
• Manage change control system and ensure that any changes are logged.
• Raising deviations and non-conformances and identifying root cause and implement corrective actions.
• Consult with suppliers on non-conformities and deviations.
• Raise any out of specification or deviations with Line Manager.
• Help with any supply chain issues to help support batch release.
• Raise CAPAs as required and implement assigned actions.
• Conduct validation activities as required, including writing up protocols when required.
• Assist with internal audits.
• Suggest improvements to increase efficiency and compliance.
• Conduct batch document review.
• Regular walkabouts of facilities

The Person
• Educated to degree level within the scientific field
• Previous industry experience within quality and regulatory within either of the Pharmaceutical or Food Manufacturing environment.
• Experience of GMP or HACCP
• Forward thinker with ability to roll up your sleeves' and get stuck in.
• Ability to work within a team, but also independently.
• Keen to learn, highly driven and committed.
• Ability to learn quickly in a fast-paced environment










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