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 position The Laboratory Technician (M/F/d) ensures smooth and safe operation of the I&TD; laboratory and executes in collaboration with the relevant scientists experiments for new pipeline products development and process innovation.
Main Activities and Responsibilities Designs and executes lab research activities focusing on new product and technology development.
Also, when required, executes activities for Centrient's Strain Conservation Unit.
Manages the I&TD; laboratory, ensuring the right equipment is available and in technical good shape for seamless execution of all ongoing research.
Maintains quality system and ensures good traceability of data, implementing lab management best practices.
Maintains relations with all suppliers and key stakeholders for the above.
Ensures that all activities comply with legal regulatory requirements and company QESH (Quality, Environment, Safety and Health) policy.
Participates in scale-up and tech-transfer.
Requirements University degree in a relevant life science field such as Biotechnology, Microbiology or similar.
Minimum of 2-3 years' experience in relevant pharmaceutical industry.
Fluent proficiency in English language (written and spoken).
Experience in Lab management and safety.
Project management experience required.
Good understanding of GMP practices & requirements.
Excellent organizational skills.
Strong conceptual and analytical skills.
Ability to work in a global environment.
Benefits 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 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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