Recruitment Fraud Alert
Takeda has received reports that there are instances of identity thieves posing as Takeda employees in an attempt to steal personal information from job seekers. In these cases, identity thieves visit job-related websites and invite candidates to online chats. During the chat, they press job seekers to provide bank account information and personal identification numbers. If you receive unexpected offers of employment from people claiming to work for Takeda, we suggest you do not correspond with them, do not click any hyperlinks and do not open any attachments.
At Takeda, we will never ask for personal financial information during any step of the interview nor do we charge job seekers fees as part of the recruitment process. Takeda’s recruiting correspondence will be sent by a recruiting representative with an @takeda.com email address – not @gmail.com, @yahoo.com, @hotmail.com or any other email domain service.
If you believe you have been contacted by an unauthorized person, please contact your local law enforcement agency immediately.
Qualified Person (Ninlaro)
The Qualified Person (Ninlaro) is a key member of the Quality Assurance team associated with production of oral solid dosage product (Ninlaro) at Takeda Ireland Limited Grange Castle (TILGC). In particular, the Qualified Person (Ninlaro) will assume the role of Qualified Person for the release of Ninlaro product in accordance with EU Directive 2001/83/EC.
In accordance with business needs, the Qualified Person (Ninlaro) may assume responsibilities in any other work area of the TILGC Quality Department.
As with all site personnel, the Qualified Person (Ninlaro) is responsible for promoting a culture of Regulatory Compliance and Continuous Improvement within the Quality Department and across the TILGC site.
The responsibilities of the Qualified Person (Ninlaro) include the following:
Management of batch disposition and material status control activities associated with Ninlaro, acting as a site Qualified Person.
Management of review of Batch Manufacturing Records (BMRs).
Assisting in, and facilitating, investigations as part of the site Deviation Management System, ensuring effective root cause analysis and assigning of appropriate CAPAs.
Co-ordination of the Change Control process associated with Ninlaro production, ensuring controlled implementation of all GMP related changes.
QA oversight of routine manufacturing, testing and relating activities to ensure ongoing cGMP compliance.
Ensuring effective participation of the Ninlaro Quality Assurance team in production and other site meetings.
Implementation of Key Performance Indicators within the Quality Assurance area to align with company and global quality objectives.
Participation in the site Internal Audit programme.
Participation in the preparation of, and hosting, external cGMP audits, e.g. from Regulatory Authorities and Global Quality.
Participation in the preparation of documentation for regulatory submission and participation in regulatory affairs discussions.
Taking a leadership role in promoting a culture of Compliance, Right First Time and Continuous Improvement.
Implementing efficiency improvements in Quality Dept on a continuous basis and participating in site projects and initiatives.
Communication and liaison with other TILGC departments on Quality issues (as required), providing guidance and support to others.
Acting as a designee to the Quality Executive (Ninlaro) as required.
Participate fully in any cross functional training initiatives.
Drive and promote the corporate values of Takeda-ism within the workplace.
Actively foster, in cooperation with other staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business. Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
Ensure timely completion of all SOP, reading, training and assessment.
Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
Primary Degree in a scientific discipline
Must meet the educational requirements of a Qualified Person as per EU Directive 2001/83/EC.
Minimum of 5 years' experience in the pharmaceutical industry in a Quality role.
Experience of oral solid dosage manufacture.
SKILLS / COMPETENCIES:
Excellent knowledge of Good Manufacturing Practice as described in current FDA & EMEA regulations for oral solid dosage pharmaceutical manufacture.
High level of initiative.
Excellent verbal and written communication skills.
Strong project management and organisational skills.
Ability to adapt to changing priorities.
Qualified Person status is essential.