Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra.
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 over 2000 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.
Summary
Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra.
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 over 2000 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.
As a part of the Quality Department in the Dechra Manufacturing & Supply Division (DM&S), the Quality Technology Manager is responsible for defining and managing the execution of the GxP Computerised System Life-Cycle for the for all GxP software & computerized technology being implemented at the divisional level (i.e., SaaS software packages) ensuring compliance with the applicable regulations including computer system validation and data integrity. Additionally, the role works collaboratively with stakeholders supporting the IT/digital Roadmap and with the wider quality organisation to monitor the effectiveness of the validation and operational quality activities associated with automated systems.
So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:
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:
Educated to Degree level (or equivalent qualification/experience) in relevant science based or comparable discipline.
Pharma/Biotech industry experience with 10+ years' experience in technology- Management/leadership experience.
Strong leadership skills with the ability to challenge, influence, and build consensus.
A strong track record of establishing and maintaining validation processes/systems which facilitate the delivery of qualification/validation activities to the required quality and regulatory standards.
In depth knowledge of relevant regulatory agency guidance in relation to Computer Systems Validation, including FDA, EMA, GAMP, ICH and authorities in other major geographic areas, is essential.
Previous experience of participating in regulatory agency inspections and general auditing.
Proven ability of accurate and timely completion of tasks.
Excellent verbal, written and interpersonal communication in English.
Proven ability to be able to manage changing situations with efficiency, calmness, and purpose with the thought to all parts of the business using knowledge of the business and customers to assist.
Frequent global travel is required with this role.
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