Manufacturing Science Technology
hace 3 semanas
At Centrient Pharmaceuticals, we are a leading manufacturer of beta-lactam antibiotics and a provider of next generation statins and anti-fungals. Our mission is to improve lives through innovative and sustainable manufacturing of medicines. We are committed to Quality, Reliability, and Sustainability in everything we do.
We have a unique opportunity for an experienced professional to join our team as a Manufacturing Science Technology & Process Improvement Leader. As part of our global operations, you will be responsible for ensuring the portfolio is maintained in a validated/compliant status across the product lifecycle. This includes developing portfolio risk assessments and implementing annual continuous improvement plans for marketed products.
This role involves technical coordination/support with Contract Development and Manufacturing Organizations (CDMOs) and other departments within Centrient. You will act as a Subject Matter Expert (SME) across Centrient on all product, process, and technology-related matters, ensuring compliance with industry regulatory/quality guidelines. Additionally, you will lead technology transfers as part of network optimization/portfolio expansion plans and be responsible for project teams.
You will be expected to build and maintain an adequate external network to deliver on customer commitments and long-term growth plans. This involves representing the technology function in Europe, the Middle East, and Africa (EMEA) with coordination across Centrient and 3rd parties. You will also be responsible for providing technical due-diligence support on portfolio/asset acquisitions and evaluation of new to network CRO/CDMOs.
In this challenging and comprehensive operational environment, you will have many opportunities for personal input and growth. You will work in an open, direct, and informal atmosphere with a lot of freedom and responsibility. The organization is very flat, allowing for easy communication and collaboration. We offer a local contract with a competitive salary estimated at $120,000 per year, based on location and experience.
To succeed in this role, you will need at least 10 years of experience in Pharmaceutical Technology, preferably in generics. You should hold an academic degree (MSc) in Technology, Pharmacy, Biochemistry, or a related field. Advanced degrees are preferred. You must have broad, multidisciplinary experience and be well-trained in all relevant Quality and Safety policies and procedures. Managerial and social knowledge and experience are essential. Having extensive experience in pharmaceutical production, analytical chemistry, and collaborations with third parties is highly desirable. You should also have a drive for results, passion for success, and a willingness to Improve, Innovate, and Change.
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Barcelona, Barcelona, España Empresa Reconocida A tiempo completoCompany OverviewCentrient Pharmaceuticals is a leading manufacturer of beta-lactam antibiotics and a provider of next-generation statins and anti-fungals. With a rich history dating back 150 years, the company has evolved from 'Nederlandsche Gist- en Spiritusfabriek' to become a global player in the pharmaceutical industry.About the RoleWe are seeking an...
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