Quality Assurance StudentWicklow, Leinster
At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization. It’s reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines and our BioLife Plasma collection network. When you’re a part of our team, you’ll do meaningful work that makes an impact on the lives of patients. Learn more about us and explore the opportunities to build a remarkable career.
Working with the Quality team to help maintain quality standards throughout the company. The brief requires knowledge of Good Manufacturing Practice, current FDA and EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes and packaging processes used in the pharmaceutical industry.
To assist in the investigation into non-conformances, participate in root cause analysis and carry out quality review of non-conformances
Preparation and revision of cGMP documentation as required including;
Annual Product Reviews
Standard Operating Procedures
Technical Reports and Protocols
Support the site Quality Management systems including;
Non-Conformance and CAPA Management systems
Change Control system
Internal Auditing programs
Vendor Management program.
Participate in and facilitate continuous improvement projects as required
Control/storage of retain samples, including periodic retain inspection
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 TIL 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.
Studying towards a degree in a scientific discipline or other relevant course.
Experience in the pharmaceutical industry would be preferable but is not essential.
- Excellent verbal and written communication skills.
Be self-motivated, flexible, organized and a good team player with the ability to prioritize own work based on departmental and site requirements.
Worker Sub-TypePaid Intern (Fixed Term) (Trainee)
Time TypeFull time
Working at Takeda
InclusionHere, you will feel welcomed, respected, and valued as a vital contributor to our global team.
CollaborationA strong, borderless team, we strive together towards our priorities and inspiring mission.
InnovationBold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.
Top WorkplaceRecognized for our culture and way of working, we’re one of only 15 companies to receive Top Global Employer® status for 2023.
Work-LifeOur people-first mission extends beyond patients to include their families, communities, and our own Takeda family.
EmpowermentThrough trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
Create an exceptional people experience.
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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