Job SummaryThe Associate Director Bioassay and sample management provides strategic leadership and management to deliver Immunogenicity and Efficacy data across the global portfolio of Seqirus clinical Trials. He/She/they will ensure all Immunogenicity and Efficacy activities are successfully planned, implemented and completed in accordance...
Job SummaryThe Associate Director Bioassay and sample management provides strategic leadership and management to deliver Immunogenicity and Efficacy data across the global portfolio of Seqirus clinical Trials. He/She/they will ensure all Immunogenicity and Efficacy activities are successfully planned, implemented and completed in accordance...
342141 Regulatory Global Submission Manager / Project Manager This is an excellent opportunity for either an established Project Manager in the Life Sciences industry or Regulatory Affairs professional looking to join a truly global team/role working across multiple therapy areas. The job holder...
At GSK, we're a company with a purpose to help people do more, feel better and live longer. We realise that our purpose starts with us. When we feel at our best, we perform at our best. Therefore, we want all...
Site Name: Italy - Siena Posted Date: Aug 22 2022 ‘Be You’ at GSK Uniting science, talent, and technology to get ahead of disease together At GSK, we have already delivered unprecedented change over the past four years, improving R&D;,...
**Site Name**: USA - Massachusetts - Cambridge, Italy - Siena **Posted Date**: May 6 2022 The **_Vx R&D; Operations Manager_** is a key role which supports the Vaccines R&D; Leadership Team. We bring: \- **FOCUS**: Utilizing our tenacity, experience,...
**Site Name**: Italy - Siena, Belgium-Wavre, USA - Maryland - Rockville, USA - Pennsylvania - Upper Providence **Posted Date**: Feb 11 2022**_ ‘Be You’ at GSK_** Uniting science, talent, and technology to get ahead of disease together At GSK,...
Would you like to drive change and transformation efforts that enable successful regulatory outcomes for GSK? If so, this Regulatory Affairs Operations Manager role could be an ideal opportunity to explore. As Regulatory Affairs Operations Manager, you will manage multiple projects and teams...
This is an exciting opportunity for a brilliant PhD level scientist to join a world leading Vaccines Research & Development environment. You'll be channeling your passion for science and helping to revolutionize the future of Vaccines R&D; at GSK whilst fostering strong...
Why GSK Uniting science, technology and talent to get ahead of disease togetherGSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health...
Job description The Commissioning, Qualification and Verification (CQV) Engineer has a hands-on attitude, motivated, accurate and responsible for the CQV part in projects. The CQV Engineer communicates at all levels within the organization and has a sound (design) experience in pharmaceutical engineering, equipment...
At GSK, we're a company with a purpose to help people do more, feel better and live longer. We realise that our purpose starts with us. When we feel at our best, we perform at our best. Therefore, we want all...
GSK Siena - 9 ore fa talent.com Directs the CMC regulatory activities of multiple projects. As Senior Manager, CMC Regulatory Vaccines Mature Products, your key responsibilities are: You drive the CMC strategy, coordinates thetimelypreparation and authors, as needed, technical (CMC) regulatory documentsto support development and registration of newvaccines or lifecycle activities and maintenance of registered vaccines,in...
Pipeline Project Manager, Associate and Director Pipeline Project Managers We are seeking talent for multiple opportunities within our Pipeline Project Management Organization to include Pipeline Project Managers, Associate Directors and Directors.When applying for this role, please use the ‘cover letter’ of...
Site Name: Italy - Siena Posted Date: Sep 20 2022 Be You’ at GSK Uniting science, talent, and technology to get ahead of disease together At GSK, we have already delivered unprecedented change over the past four years, improving R&D;,...
Regulatory Manager, CMC Vx Mature Products GSK Siena - 10 ore fa talent.com You will be responsible for the CMC regulatory activities of multiple projects. Key responsibilities: You drive the CMC strategy, coordinates the timely preparation and authors, as needed, technical (CMC) regulatory documents to support development and registration...
As Manager, Global Regulatory Affairs, your key responsibilities are: Provide support to the Global Regulatory Lead (GRL) for key regulatory activities pertaining to a project/product Interact with (or represents his/her area/product at) internal project related teams (e.g. CRT, SRT, etc.) and possibly project...
Site Name: Italy - Rosia Posted Date: Sep 20 2022 Be You’ at GSK Uniting science, talent, and technology to get ahead of disease together At GSK, we have already delivered unprecedented change over the past four years, improving R&D;,...
AMPLIA is a multinational company based in Portuguese and stablished since 2015, with native consultants in Portugal, Italy, Romania, Poland, Bulgaria and Spain. We are specialists in career management and recruitment of professionals in Hospitality in several countries (Europe, Middle East and United...
Role summaryThe Safety Evaluation & Risk Management (SERM) Head leads a global team of physicians and scientists overseeing the clinical safety and pharmacovigilance activities for a group of assets in the Vaccines portfolio. The role reports to the Vice President and Head...
