Quality Laboratory Professional (12mth FTC)

Fantastic opportunity to work as a Professional in the Quality Laboratories at LEO Pharma Dublin. 

Shape the LEO Pharma of tomorrow 
At LEO Pharma, our mission transcends the conventional. We're on an ambitious path to become the leaders in medical dermatology worldwide. 

In Quality Laboratories we share a “challenge accepted” mindset and are guided by our winning behaviours of simplification, collaboration, and accountability, to achieve our goals

Your new role

The Professional role will support the Laboratories in reviewing and certifying batch paperwork in a timely and satisfactory manner. To support and drive improvement projects within the lab groups and to support requests made by external stakeholders. To act as cover for the Associate Manager in the event of a planned or unplanned absence. Responsibilities will include but not limited to: 

• The review and certification of laboratory batch paperwork in line with a high standard of schedule  adherence. 
• Driving Lab investigations into out-of-spec and/or out-of-trend results at the Laboratories and for assisting in the closing out of CAPAs, Deviations, and other quality actions at the Labs. 
• Participating in improvement projects designed to improve laboratory processes and adherence to schedules and the demands of external stakeholders.
• Implementing a right first time and safety-first approach within the lab groups.
• Assisting in and preparing APQR reports in line with industry requirements. 
• Assisting in and/or performing equipment qualification and calibration in the Laboratories. 
• Assisting in method transfers within the lab group when the need arises.
• Contributing to the Laboratory Archive procedure via the processing, collating, and filing of  laboratory batch paperwork.
• Promoting healthy internal and external communication relating to the Lab group. 
• Facilitating MSAT investigations and for assisting in root cause analysis measure when needed. 
• Assuming ownership of quality management actions and for ensuring that timeliness is maintained to a satisfactory level in line with laboratory trends for quality events. 
• Review of pharmacopeias (including updates) and ensuring that laboratory documentation (SOP’s, WI’s, TM’s, Specifications, etc.) and practices are in compliance with the current versions of the pharmacopeias

Your qualifications

To succeed in this role, we imagine that you have the following qualifications: 

• Minimum B.Sc. in a relevant science discipline
• Proven experience in the Pharmaceutical Industry.
• Computer proficient to allow for optimal results in the areas of process ownership and change management. 

LEO Pharma is built on collaboration, innovation and curiosity. Is this you? Can you bring this and continuous improvement mindset? 

Your application

You do not need to upload a cover letter, but feel free to add a few sentences in your resume or CV on why this position has your interest.