Summary Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.
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 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 Opportunity Reporting to the QC Manager and managing a team of Analysts and Senior Analysts, you shall enhance laboratory practices and promote a culture which is consistent with cGMP, cGLP and Health & Safety within a pharmaceutical laboratory environment.
Responsible for leading the Quality Control laboratory shift resources to achieve the required organisational throughput in a compliant and effective manner Main Responsibilities So, what will you be doing?
This role has a broad and varied remit and the successful candidate will have responsibility for duties including: Day to day management of the QC shift team, including: Staff performance and wellbeing, including routine 1-2-1s, target setting, and coaching individuals through any development needs.
Coordinate resource priorities with Planning to achieve schedule adherence.
Manage the throughput of inbound and outbound goods (primarily raw materials, intermediates and finished products) within the department.
Support validation activities.
Determination of KPIs that support delivery to service level agreements and achievement of objectives.
Clear presentation of KPI data.
Identification and management of risks.
Preparation and scrutiny of reports (routine and ad-hoc), as required, to peers and senior management.
Effective communication with other departments to facilitate the progression of QC activities.
Lead investigations in to out of specification (OOS), out of trend (OOT) and a-typical results by applying technical knowledge and problem-solving skills.
Ensure Quality Control activities are performed consistently, on time and in accordance with both company and legal requirements.
Actively seek opportunities to optimise the performance of processes, people and other resources.
Support the QC Manager with the hosting of departmental audits and inspections, including: Presenting the department and systems to an inspector.
The compilation of responses.
Ensure response commitments are fulfilled.
Support the QC Manager in the delivery of departmental objectives and deputise, when required.
Abide by and champion the company's values (Dedication, Enjoyment, Courage, Honesty, Ambition) in all aspects of the role, including interaction with co-workers and third parties.
In addition to the core responsibilities listed above, the jobholder may be required to perform other duties on an ad-hoc basis.
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: Experience of working within a pharmaceutical laboratory.
Experience of leading and managing a team, with a focus on coaching/mentoring.
Experience in chemical and instrumental techniques, such as; traditional wet chemistry, spectroscopy, chromatography, Karl Fischer, TOC, pH, etc.
The ability to troubleshoot on the majority of the above / good problem-solving ability.
Effective communication and influencing skills.
Pragmatism.
Computer literate with good attention to detail.
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