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QC Project Team Leader
1 month ago
Dechra is seeking a highly skilled QC Project Team Leader to join our Skipton site. As a key member of our Quality Control team, you will be responsible for leading a team of project analysts to optimize test regimes on products.
Main Responsibilities
Lead a team to deliver project objectives to expected timelines
Coach and mentor team members to develop relevant skill sets
Review specifications to ensure non-value adding tests are removed from the finished product specification
Redevelop tests to run more efficiently, better supporting the testing of high numbers of samples at one time
Redevelop tests to run on more efficient equipment
Write development protocols and reports
Perform validation and verification, including producing protocols and reports
Submit updated test regimes to regulatory authorities, including justification of specification
Manage updates to methods, specifications, and test records in Quality Control
Lead change controls
Utilize technical knowledge to train and coach project analysts to enable them to support project goals
Liaise with MS&T, QC Support, Regulatory, and QA
Act as subject matter expert in QC for Method Development in HPLC, UPLC, UV, Dissolution, Disintegration, Friability, Hardness, Loss on Drying, FTIR, Karl Fisher, and pH
Conduct laboratory investigations, protocol deviations, and provide technical expertise to troubleshoot challenging methods
Author Risk Assessments for processes, procedures, and systems to ensure risks are identified and appropriately managed, including mitigation via corrective and preventive actions (CAPAs), where appropriate
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
Enhance practices and promote a culture consistent with cGMP, cGLP, and Health & Safety within a pharmaceutical laboratory environment
Requirements
Educated to HNC/D level in a relevant scientific subject or possesses significant job-specific experience
3 years' experience working in method development in a pharmaceutical GMP environment
GMP regulations for products produced, tested, and marketed within the UK, EU, and US
Knowledge of specification setting
Computer literate, with an attention to detail (inc. formatting) and clarity
Effective and tailored communication
Influencing
Problem-solving
Pragmatism
Attention to detail
About Dechra
Dechra is a growing, global specialist in the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing, and sales of high-quality products exclusively for veterinarians worldwide. It's a great time to join our modern Skipton facility as further investment for the Skipton site means that we're in an exciting period of positive change for the business. Here at Dechra, our values are embedded within our culture and thrive within our family of almost 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.
