Analytical Development Technician
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 Technician (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 Technician works together with the Analytical Development Scientist on the development, validation and transfer robust analytical methods (sample preparation, chromatographic analysis, spectroscopic techniques, PSD analysis, etc…) to support the development of API and its intermediates, scale up, process validation, tech transfer, pre-stability and stabiltiy studies. Follow protocols, write reports and work electronic notebook with test results obtained in the analysis and studies performed.
The main activities and responsibilities
- Analysis of samples from the development phase and incoming products (KSM, reagents, etc.) as well as scale up and exhibit batches. Analysis of stability samples.
- Development and optimization of analytical methods for quality control of APIs and its intermediates.
- Interpretation of analytical data for decision making.
- Validation, verification and transfer of analytical methods.
- Support to the QC department during method transfer.
- Complete ELN with the necessary primary data according to the data integrity requirements.
- Acts as contact person for the assigned Laboratory Instruments.
- Control and management of stock of reagents, solvents, consumables and standards.
Requirements
The Ideal Candidate
- Technical Degree (FPII) or Higher Technician Certificate degree (CFGM / CFGS) in laboratory analysis and quality control.
- Minimum of 5 years of experience in process development in chemical or pharmaceutical industry.
- Intermediate level of English language (written and spoken).
- Knowledge of GMP, HPLC/UPLC and GC.
- Adaptable, self-motivated and curious systems thinker.
- Results oriented.
- Proactive and team work attitude.
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 HRSpain@centrient.com. 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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