junior regulatory associate jobs in Hillingdon

When our values align, there's no limit to what we can achieve. Are you passionate about regulatory affairs in the life science industry? Do you thrive in a dynamic team environment and enjoy managing complex projects? Parexel is seeking a talented Senior Regulatory Affairs Associate with biologics or vaccines background to join our growing team! As a Senior Regulatory Affairs Associate CMC at...

You will be responsible for varying levels of product support, including leading projects, based upon their experience level. Key responsibilities include: Contribute as a key member of the global regulatory CMC product team Interact with authors/reviewers and subject matter experts with respect to delivery of regulatory documents required for regulatory submissions

You will be responsible for varying levels of product support, including leading projects, based upon their experience level.

You will drive simplification, innovation, and an improved end-user experience by aligning learning technologies with business needs, regulatory expectations, and organizational priorities. The responsibilities of the role will include: - Execute the GxP Learning strategy by partnering with stakeholders to assess needs and deliver effective, technology-based learning solutions.

You will be provided with access to a 1hour online revision workshop prior to sitting your exam. This qualification will set you on a route to becoming a Chartered Project Professional with additional study and experience.

You will be provided with access to a 1-hour online revision workshop prior to sitting your exam.

You will collaborate cross-functionally with Clinical Development, HEOR, Market Access, Public Affairs, Marketing as well as with external clinicians and decision-makers. This role will report to the Multiple Myeloma Strategy Lead. Key responsibilities Partner within the Strategy Team to execute on required tasks and activities, deputising for them when required

Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of...

Description Kite is seeking a highly motivated technical expert to join our External Manufacturing Science & Technology (MSAT) team within the network MSAT unit as Associate Director, Process Engineering. The role will provide technical oversight and leadership for external manufacturing partners producing our viral vector(s) and will serve as a key liaison between Kite and our UK-based...

You will play a pivotal role within the Residential Conveyancing department, supporting a diverse client base and progressing your professional development. Key Responsibilities in Residential Property Law - Managing your own caseload of residential property transactions, including sales, purchases, transfers of equity, shared ownership, remortgage, right to buy, and new build matters.

You should bring 14+ years of progressive proven experience, including 9+ years in clinical research, regulatory, or field-based functions within the pharmaceutical or biotech industries. A strong scientific background and expertise in Medical Affairs, Clinical Research, or related areas are highly desirable.

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration,...

A leading biotechnology company in Uxbridge is seeking a Senior Associate in Regulatory Affairs to join their team. This role involves contributing to global regulatory CMC product teams, preparing regulatory submission documents, and coordinating with various teams to ensure compliance. Ideal candidates will have a relevant Bachelor's degree, knowledge of regulatory processes, and strong...

You will be provided with access to a 1hour online revision workshop prior to sitting your exam. This qualification will set you on a route to becoming a Chartered Project Professional with additional study and experience.

You will be provided with access to a 1-hour online revision workshop prior to sitting your exam.

You will play a pivotal role within the Residential Conveyancing department, supporting a diverse client base and progressing your professional development. Key Responsibilities in Residential Property Law - Managing your own caseload of residential property transactions, including sales, purchases, transfers of equity, shared ownership, remortgage, right to buy, and new build matters.

Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires...

Description Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where...

You will drive simplification, innovation, and an improved end-user experience by aligning learning technologies with business needs, regulatory expectations, and organizational priorities. The responsibilities of the role will include: - Execute the GxP Learning strategy by partnering with stakeholders to assess needs and deliver effective, technology-based learning solutions.

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of...

A leading biotechnology company is seeking a Senior Associate in Regulatory Affairs, specializing in Chemistry, Manufacturing and Controls (CMC). This role involves contributing to product development and managing regulatory strategies for submissions across multiple phases. The ideal candidate will hold a relevant Bachelor's degree and possess strong project management skills, along with...