Analytical Development Scientist
hace 2 semanas
Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals.
We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms.
We stand proudly at the centre of modern healthcare, as a maker of essential and life-saving medicines.
With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 2200 employees work continuously to meet our customers' needs.
We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.
Founded 150 years ago as the 'Nederlandsche Gist- en Spiritusfabriek', our company was known as Gist Brocades.
Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico.
Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.
The Innovation & Technology Development department has a vacancy in its team for the following position: Analytical Development Scientist (Innovation & Technology Development) The Innovation and Technology Development (I&TD) team is expanding capabilities and key competences, with analysis identified as critical tool to deliver into our innovation journey.
The Analytical Development Scientist carries out the development, validation and transfer of new analytical methods (sample preparation, chromatographic analysis, spectroscopic techniques, PSD analysis, etc.)
and analytical techniques to support the development of API and its intermediates, scale up, process validation, tech transfer, pre-stability and stability studies.
Supports the different projects from the analytical point of view.
The main activities and responsibilities Development, validation and transfer of analytical methods.
Editing and revision of ICH stabilities and validations documentation.
Investigation of analytical incidents and OOS reports.
Participation in the industrialization of new processes.
Participation in I&TD project teams.
Collaboration in Master Plans for Validation / Homologation.
Editing and reviewing the regulatory documentation necessary to support new registrations and variations.
Project management within the industrial pharmaceutical development environment.
Requirements The Ideal Candidate Bachelor's and/or Master's degree in a relevant life science field such as Chemistry, Biochemistry, Pharmacy or similar.
Minimum of 5 years of experience in method development and validation preferably in pharmaceutical industry.
Fluent in English language (written and spoken).
Knowledge of ICH and GMP.
Experience in the development of projects in the R&D area.
Adaptable, self-motivated and curious systems thinker.
Decision making and results oriented.
Strong communication skills.
Terms and reward We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals.
The organization is very flat.
You have a lot of freedom and responsibility in an open, direct, and informal atmosphere.
The Procedure Please submit your application via the 'apply' button and upload your CV & cover letter in English.
We also ask you to include information on your current remuneration.
Only applications with CV and Cover Letter will be considered.
For more detailed information about the role and about the Recruitment & Selection process you can contact us via ******.
We invite you to visit our website www.centrient.com for information about our company.
Reference check procedures are part of the Centrient Recruitment & Selection Process.
You will be contacted when a reference check is required.
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