Compliance Specialist

Description

Job Description

Compliance Specialist

Petersfield

Days 8.15am – 4.30pm Mon day – Friday

Description

My client is currently recruiting for a Compliance Specialist within the Quality Department to join an experienced and committed team. A global manufacture of makeup, fragrance and skin care.

The successful candidate will be responsible for implementing policies, procedures and standards at a site to ensure compliance with regulatory and corporate requirements. This includes management of GMP document control systems, development of annual product review reports, administration of the compliant program, supporting site audits and development & delivery of GMP trainings.

Requirements

Experience in a regulated industry is required, cosmetic or pharmaceutical experience a plus. Experience with improving Quality Systems required Experience with authorizing and maintaining procedures and work instructions is required Knowledge of compliance, related to all applicable Quality Systems Standards national and international, is required Creative individual with excellent trouble shooting skills Strong oral and written communication skills with ability to appropriately communicate information to cross functional stakeholders Ability to work in a team setting and independently under minimal supervision Ability to work in fast paced environment supporting the quality assurance/quality control departments Proficiency in Microsoft Office Suite, Electronic QMS, e–training systems and SAP systems is preferred Key Roles & Responsibilities

Implement and ensure adherence to policies, procedures and standards site wide Maintain knowledge and understanding of applicable GMP regulations, regulatory agency guidelines, industry association guidelines, Corporate requirements and best practices Conduct Internal audits ensuring actions are documented, addressed and tracked appropriately GMP Audits Hygiene audits QMS internal audits 3rd Party audit management / follow up and corrective action plans Veeva Quality One (EQMS) Quality role – reviews / approvals for CAPA, Deviations / INC / INV & Change controls Veeva Quality One (EQMS) site representation with Global team / SME

OpenText (Document management system) review / approval / system Admin

General QMS oversight driving continuous improvement across all departments against defined KPIs Identify other areas for CI utilising audit results / trends and observations Quality risk assessment programme implementation Validation protocols Quality role – review / approval Global Compliance team liaison / site representation Annual Product Reviews

Characteristics of a successful candidate:

Experience in a regulated industry is required, cosmetic and pharmaceutical experience a plus

Experience with improving Quality Systems and process design is required

Experience with authorizing and maintaining procedures and work instructions is required

Knowledge of compliance, related to all applicable Quality Systems Standards national and international, is required

Ability to build and deliver training modules

Creative individual with excellent trouble shooting skills

Strong oral and written communication skills with ability to appropriately communicate information to cross functional stakeholders

Ability to work in a team setting and independently under minimal supervision

Ability to work in fast paced environment supporting the quality assurance/quality control departments

Proficiency in Microsoft Office Suite, Electronic QMS, e–training systems and SAP systems is preferred

Ad ID: 5418393053