Qualified Person - Skipton, United Kingdom - Dechra Pharmaceuticals PLC

Dechra Pharmaceuticals PLC

Verified Company

Skipton, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

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Description

Job Introduction
Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra Pharmaceuticals PLC.

Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.

Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally.

From manufacturing to marketing, (
D)edication, (
E)njoyment, (
C)ourage, (
H)onesty, (
R)elationships and (
A)mbition are at the heart of our everyday operations and the way we do business.

The role also offers a great flexible work policy.

The Opportunity
Main Responsibilities

Driving the transformational quality culture initiatives across the site across the site by liaising with cross functional teams.
Through active engagement with the divisional Quality team and external stakeholder groups, define GxP practices and standards for the site and lead gap assessments and improvement projects as required.
Provide Quality leadership to crossfunctional teams working on FMEA, root cause analysis, and other investigative tools to ensure an holistic and systemic quality approach is imbedded in everything we do.
Escalate to the Head of Quality and SLT any trends and quality issues that are detected during batch review, systemic in nature or observed in operations.
Work with Group Regulatory Affairs by providing expert GMP advice regarding new submissions and variations / supplements.
Participating in internal and external audits, and support vendor quality management activities both at site and divisional level.
Provide leadership and participate in internal and external, and other regulatory agency inspections (UK, US, EU,etc.)
Eligibility to perform the duties of a Qualified Person under the provision of Directive 2001/83/EC, Directive 2001/82/EC, Directive 2001/20/EC and Statutory Instruments (SI , SI and SI
Extensive experience in Pharmaceutical quality department.
In depth knowledge of licensed products, processes and legislation.
Previous experience working with MHRA/VMD, FDA and participating in regulatory agency inspections.
Strong project management and time management skills.
Excellent knowledge of global pharmaceutical legislation.
High impact and influencing skills.
Excellent interpersonal and communication skills.
High levels of attention to detail, with the ability to work accurately in a busy and demanding environment.

About The Company