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We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
Discover more about our company wide benefits and life at (COMPANY NAME) on our webpage Life at (COMPANY NAME) | (COMPANY NAME)
We've had an exciting opportunity within our Vaccine Global Drug Product Technical R&D team to work as Scientific Leader on a permanent, full-time basis. This role is pivotal in shaping and executing global strategies for Drug Product Characterization and Process Analytical Technologies (PAT).
As a Scientific Leader, you will be responsible for generating science-based insights into product characteristics and enhancing product/process understanding. Your role will involve designing tailored characterization approaches and spearheading the adoption of innovative analytical tools, by develop people capabilities through matrix leadership. These efforts will support Drug Product development by generating timely data to construct robust drug products by design.
You will also play a key role in the adoption of emerging technologies to accelerate clinical program development. This includes leading the creation of funding proposals for resources and CAPEX to meet scientific workstream milestones.
Your influence will extend to fostering collaborations to access innovative technologies, influencing portfolio progression through the introduction of new technologies into product development programs, and shaping regulatory and commercialization strategies.
Furthermore, as a Scientific Leader, you will lead, design, and execute scientific studies in support of technical development programs. You will represent Drug Product in the Technical Development Team for complex projects, author regulatory source reports, and contribute to the writing and reviewing of regulatory submissions.
Join us in this exciting role and contribute to the future of Product Development.
Why you?
Basic Qualifications & Skills:
* PhD with 3+ years of post-doc and/or job-related experience, with experience in Vaccine/Biotech technical development and understanding of secondary unit operations;
* Understanding of drug product degradation pathways;
* Knowledge on mass-spectrometry, spectroscopic, chromatographic, compositional analyzers, fixed purpose sensors and continuous process;
* Knowledge on automated and statistical data analysis, chemometrics and overall Quality by Design principles.
* Excellent intercommunication skills
* Fluency in English
CLOSING DATE for applications: June, Wednesday 26th. We will be accepting applications up until the closing date, however, please note that we will be processing applications and scheduling interviews during the advertising period. Your application would be welcomed as soon as possible.
Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.
The position offered will reflect the actual competence and experience gained by the identified candidate, in relation to the responsibilities of the proposed role.
Internal candidates can apply through the My Job Opportunities section in Workday. We remind you that it is necessary to inform your manager when you are called for the selection interview.
Why (COMPANY NAME)?
Uniting science, technology and talent to get ahead of disease together.
(COMPANY NAME) 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 of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making (COMPANY NAME) a place where people can thrive. We want (COMPANY NAME) to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at (COMPANY NAME), please contact the (COMPANY NAME) Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).
(COMPANY NAME) is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies
(COMPANY NAME) does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact (COMPANY NAME)'s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to (COMPANY NAME). The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and (COMPANY NAME). In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of (COMPANY NAME). (COMPANY NAME) shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, (COMPANY NAME) may be required to capture and report expenses (COMPANY NAME) incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure (COMPANY NAME)'s compliance to all federal and state US Transparency requirements. For more information, please visit (COMPANY NAME)'s Transparency Reporting For the Record site
