Improve & Projects Engineer
hace 3 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 position
The role shall develop and manage all aspects of Centrient Pharmaceuticals Spain Continuous Excellence, its activities and projects. Contribute to the site strategy and policy in general and specially to Continuous Improvement activities.
Main activities and responsibilities
- Setup, implement and report Continuous Improvement program, according to the objectives and priorities agreed with Site Director.
- Lead activities and projects related to Operational Excellence and Continuous Improvement.
- Ensure that improve procedures are performed and documented in full compliance with cGMP and SHE Centrient standards and according to site SOPs and Centrient Corporate Compliance Policies.
- Yearly preparation of improvement program.
- Coach, develop and train Centrient Pharmaceutical Spain organization with regard to Continuous Improvement and Operational Excellence tools.
- Encourage the organization to improve.
- Coordination of the Improvement Ideas Tool (IDM).
- Ensure the quality and update of technical documentation.
**Requirements**:
- University degree in Engineering, Chemistry, Biochemistry, Biotechnology.
- + 3 years in Continuous Improvement (preferred in chemicals or pharmaceutical companies).
- Fluent proficiency in Spanish and English (written and spoken).
- Strong in communication and presentation skills.
- Experience in promoting cultural change, mobilize people and coaching.
- Problem-solving skills include organization, troubleshooting, trustworthiness and ethics.
- Adaptable, self-motivate and curious systems thinker.
- High learning agility and lead in a cross-functional environment.
- Project Management skills.
**Benefits**:
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
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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