Regulatory Manager, Cmc Vx Mature Products
il y a 1 semaine
Site Name:
Belgium-Wavre, GSK House, Poznan, Siena
Posted Date:
Mar 8 2023
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 of new vaccines or lifecycle activities and maintenance of registered vaccines, in accordance with the applicable regulatory & scientific standards, taking into account the evolving regulatory requirements.
- You provide regulatory advice and guidance to the Technical Development Team and/or Technical Life-Cycle Team (TLCT), Implementation Committee, Specification Review Committee, Technical Review Board, CMC Expert Panel, and provides regulatory support to their partners in R&D, Quality Control, Manufacturing, QA and Supply.
- You ensure adequate interaction and partnership with the Global Regulatory Lead's team in order to define proper regulatory CMC filing strategy.
- You ensure adequate contribution during interactions with Worldwide regulatory authorities.
- You ensure, in a continuous improvement mindset, regulatory compliance is maintained and shares bestpractices and learnings within the CMC Regulatory teams and other impacted functions.
- You may engage and lead CMC Subject Matter Expert activities, both internally (for increased compliance, harmonisation and efficiency) and externally (external advocacy and shaping the regulatory environment).
- You may mentor or train staff.
- You may participate in corporate evaluation and provide CMC regulatory support/advice to inlicensing and divestment projects.
- You may deliver CMC regulatory strategy to support major inspections (eg PAI's) or quality incidents (PIRCs).
Why You?
Basic qualifications:
- Bachelor's degree in Sciences or Medical Sciences
- Master's degree or above in Chemistry, pharmacy, biological or closely related science advanced degree.
- Regulatory Affairs Certification (e.g. RAPS)Successfully managed multiple projects simultaneously.
- Sound knowledge of drug development and manufacturing and supply processes and may have a specialized area of expertise.
- Knowledge of CMC regulatory requirements.
- Demonstrated ability to handle global CMC issues through continuous change and improvement
Preferred qualifications**:
- Experience in Pharmaceutical industry or Research organizations, established in Regulatory Affairs and with demonstrated experience of leadership in a matrix environment.
- Sound knowledge of vaccines/biological products development, manufacturing and supply processes.
- Continued professional growth in global regulatory affairs including communication of evolving/emerging trends and policies. Has identified opportunities to further educate colleagues and formulate approaches to most effectively meet new requirements.
- Highly developed interpersonal, presentation and communication skills.
- Proven experience in training staff within an organisation.
Why GSK?
GSK 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.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.
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 GSK a place where people can thrive.
We want GSK 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.- Li-GSK
If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.
GSK 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.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.
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 GSK a place where people can thrive.
We want GSK to be-
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