Job Introduction

Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra Pharmaceuticals.

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 2000 colleague 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.

Role Responsibility

So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:

Conducts activities related to recorded non-conformities and prescribed CA/PA within Genera d.d.

• records every reported non-conformity, and maintains a status table
• participates in non-compliance investigation
• records non-compliance investigation
• participates in prescribing corrective/preventive measures
• monitors the implementation of corrective/preventive measures, and records their implementation

Making changes

• Defines activities for implementing changes in the system
• Approves changes that are not subject to RA documentation
• Decides on the completion and success of the implementation of changes in the system
• Administratively records every reported change, and maintains a status table
• Monitors the implementation of changes and records their implementation

Creates documentation and reviews it

• creates and/or reviews standard operating procedures
• reviews work instructions
• reviews the protocols and reports of the qualification documentation
• creates and/or reviews validation protocols and reports
• inspects production procedures of manufacturing and equipping, production records

Performs and organizes employee training

• Educates employees according to standard operating procedures for which he is the author/co-author
• In accordance with his own professional qualifications, he conducts employee training in the area of quality system procedures

Participates in the preparation and implementation of audits

• Participates in other regulatory audits in accordance with the scope of work and responsibilities

Annual Product Quality Review (PQR)

• Making annual reviews of the quality of VMP products

GLP relevant activities:

• records every reported non-conformity, and maintains a status table
• participates in non-compliance investigation
• records non-compliance investigation
• participates in prescribing corrective/preventive measures
• monitors the implementation of corrective/preventive measures, and records their implementation

Follows domestic and international GMP and legal regulations

• Follows the guidelines given by regulatory and professional institutions (HALMED, EMA, FDA, MHRA, etc.) for their field of work
• Initiates and implements harmonization of documentation and quality assurance processes in general with GMP and legal regulations for his area of work

Performs other tasks from the scope of work of Quality Assurance, in accordance with expertise, according to the decision of the manager of Quality Assurance and the manager of Quality.

The Ideal Candidate

Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We’re particularly keen to hear from those who have/are:

• previous work experience in a similar position
• academic background in chemistry/ biotechnology or other related field
• meticulous and well organized
• excellent knowledge of the English language, both spoken and written
• good computer skills (MS Office etc.)

About the Company

All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we’re looking for. Should you not hear back from us within 28 days please don’t be too disappointed – we may keep your CV on our database for any future vacancies which may be suitable and we encourage you to keep an eye on our careers site. For any questions or queries, please contact us at recruituk@dechra.com

The legal employer on behalf of Dechra Pharmaceuticals in Croatia is Genera Inc.  

Genera Inc. is a part of the Dechra Group since 2015

Dechra Pharmaceuticals PLC