Regulatory Affairs Pro – VMS/Food Supplements (9‑Month)

Alliance Pharma PLC

Chippenham

Híbrido

GBP 32.000 - 46.000

Jornada completa

Hace 11 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

25 days annual leave
Pension scheme
Life assurance
Private medical insurance
Employee Assistance Programme
Global recognition programme

Descripción de la vacante

Alliance Pharma PLC in Chippenham, Wiltshire, offers a hybrid Regulatory Affairs Associate role (VMS/Food Supplements) for a 9-month maternity cover starting November 26. The post supports maintenance and development of an EMEA portfolio across VMS, cosmetics and medical devices.

The role requires a proactive regulatory professional with a strong VMS background, familiarity with UK/EU regulations, regulatory databases and QMS processes.

Formación

  • Degree in Life Sciences or related field.
  • Experience in Regulatory Affairs for VMS/Food Supplements.
  • Knowledge of UK/EU food supplement legislation and labeling.

Responsabilidades

  • Provide regulatory support for new product development and launches.
  • Prepare and review regulatory docs; ensure submissions to regulatory databases are compliant.
  • Support maintenance of EMEA food supplement portfolio; advise on cosmetics and medical devices.
  • Contribute to QMS activities: SOPs, audits, CAPAs and compliance initiatives.
  • Monitor regulatory developments and communicate impacts to the business.

Conocimientos

Attention to detail
Communication skills
Organisational skills
Stakeholder management
Regulatory know-how
Cross-functional

Educación

BSc/MSc Life Sciences

Herramientas

Regulatory databases

Descripción del empleo

Alliance Pharma PLC in Chippenham, Wiltshire, offers a hybrid Regulatory Affairs Associate role (VMS/Food Supplements) for a 9-month maternity cover starting November 26. The post supports maintenance and development of an EMEA portfolio across VMS, cosmetics and medical devices.

The role requires a proactive regulatory professional with a strong VMS background, familiarity with UK/EU regulations, regulatory databases and QMS processes.

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