Director, Quality And Regulatory

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. **Position Summary**: The Director, Quality and Regulatory...

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Position Summary: The Director, Quality and Regulatory will oversee...

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Position Summary: The Director, Quality and Regulatory will oversee...

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Position Summary: The Director, Quality and Regulatory will oversee...

**Director of Regulatory Development and Strategy** **UK or EU based (Hybrid working with some travel)** **Salary**: Competitive + Benefits + Bonus If you are a dynamic regulatory leader with expert technical and tactical experience in regulatory strategy in the UK, EU and internationally then we want to hear from you. Join us to help improve peoples'...

Quality and Regulatory Affairs (QA/RA) TraineeThe Quality and Regulatory Affairs (QA/RA) Trainee supports the execution of preand/or post market regulatory affairs departmental functions, including, but not limited to,assisting in the preparation of documentation and information required to place and tokeep products on the market: regulatory submissions,...

At Ipsen, we are looking for a **Medical and Regulatory Affairs Director Iberia **based in** Barcelona**. Following the general strategies of the company and the department guidelines, as well as all the procedures and policies, current legislation, code of conduct, and deontology. Your main responsibilities will be: - ** Medical Director** - To promote...

At **AstraZeneca **we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth...

At Ipsen, we are looking for a Medical and Regulatory Affairs Director Iberia based in Barcelona.Following the general strategies of the company and the department guidelines, as well as all the procedures and policies, current legislation, code of conduct, and deontology.Your main responsibilities will be:- Medical Director To promote the relationship and...

Overview Post Date November 7, Number WEBWW-- Job Function QA&RA Location Barcelona, Spain Country Spain About the Position ob Summary The Quality and Regulatory Affairs (QA/RA) Trainee supports the execution of pre and/or post market regulatory affairs departmental functions, including, but not limited to, assisting in the preparation of...

**AstraZeneca** is an innovation-driven global biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines, primarily for the treatment of cardiovascular, renal, and metabolic, respiratory, and immunological, oncological and rare diseases. In line with our firm commitment to training and developing...

AstraZeneca is an innovation-driven global biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines, primarily for the treatment of cardiovascular, renal, and metabolic, respiratory, and immunological, oncological and rare diseases.In line with our firm commitment to training and developing exceptional...

At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and...

The Associate Director – Regulatory Submissions The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...

**Scope**: Director of regulatory affairs position that has been opened to further accompany the growth of the company on this sector. Although our client is a historically pharma oriented manufacturer, they have in the recent years expanded their activities in the Medical Aesthetics area, with products currently on market in the Dermal and Hyaluronic acid...

.Job DescriptionRole holders expertly drive strategic communications excellence to achieve successful submissions and approvals. They develop innovative best practices and improvement initiatives.Typical AccountabilitiesThe Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important...

Role holders expertly drive strategic communications excellence to achieve successful submissions and approvals. They develop innovative best practices and improvement initiatives. **Typical Accountabilities** The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important...

Role holders provide strategic leadership and communications expertise to clinical drug programs. They author clinical-regulatory documents and provide critical review to achieve high quality standards. They represent the skill on drug and non-drug projects. **Typical Accountabilities** The Clinical Regulatory Writing team provides expert communications...

Quality and Regulatory Affairs (QA/RA) TraineeThe Quality and Regulatory Affairs (QA/RA) Trainee supports the execution of preand/or post market regulatory affairs departmental functions, including, but not limited to,assisting in the preparation of documentation and information required to place and tokeep products on the market: regulatory submissions,...

Quality and Regulatory Affairs (QA/RA) TraineeThe Quality and Regulatory Affairs (QA/RA) Trainee supports the execution of preand/or post market regulatory affairs departmental functions, including, but not limited to,assisting in the preparation of documentation and information required to place and tokeep products on the market: regulatory submissions,...