We are working on behalf of a global pharmaceutical company who are seeking a Stability Manager to lead and manage their Analytical Operations Stability Group. This role will be responsible for commercial stability, clinical stability, stability coordination and data trending.
What you’ll do:
You will manage the Analytical Operations Group to ensure cGMP compliance and timely completion of stability activities mainly lead by HPLC in a GMP environment.
This will provide practical, expert guidance to the team on relevant analytical techniques and applications.
The continued implementation of QRM, lean methodologies, and the programme of continuous improvement will be a key part of this role.
You will monitor Key Performance Indicators for EHS, Quality Delivery, Costs and be responsible for monthly department reporting. You will be responsible for staff appraisals within this area of responsibility, facilitating Continuous Professional Development, keeping up to date with current regulatory guidance and disseminating this within the team / ensuring up to date compliance.
You will be responsible for managing training requirements of the team, performance and absence, coaching and as necessary disciplinary.
Clients will be getting their Project Management and audit contact from you, this will also mean detailed and regular updated on forecasted revenue, capital expenditure, and accurate department budgeting. You will be responsible for the budget for your area.
GMP delivery of your area will be part of this role, and you will be again called upon in audits.
You will be educated to degree level in Chemistry, Pharmaceuticals or Life Science with leadership experience already, or strong leadership attributes, strong organisational, detail orientated and quality minded. This role will call for you to be someone who strives to improve the business via identifying opportunities to improve operations, customer satisfaction and the team.
On this occasion, LiCa Scientific is acting as an employment agency.