.EUROFINS VILLAPHARMA is seeking a HSE Manager based in Parque Tecnológico de Fuente Alamo (Murcia).
You will be responsible for enhancing quality and compliance across our organization.
In this highly visible role, you will work with leaders to identify and manage inherent and emerging risks associated with their business and to understand the current level of control within their business activities.
Your responsibilities: Working with EUROFINS VILLAPHARMA leadership team, ensure the SOP generation for each line (Scientific, Environmental, Health and Safety and other core business support) is maintained and updated.
Partner with EUROFINS VILLAPHARMA line leaders to enhance the quality culture so that people at all levels of the organization speak up when concerns, risks, or issues occur, allowing leaders to proactively address them through early mitigation.
Integrate Eurofins quality and risk management policies and programs into EUROFINS VILLAPHARMA business processes and ways of working.
Maintain risk management oversight.
Maintain contemporary knowledge of evolving regulatory expectations and global environments that impact the business.
Prioritize and escalate EUROFINS VILLAPHARMA enterprise-related risks and develop programs to mitigate and close out.
Monitor and report Performance and Compliance performance, including operational metrics.
Run L3 audits at EUROFINS VILLAPHARMA.
Prepare data for analysis and reporting purposes as required.
Liaise with the European Eurofins Compliance Officer.
We are looking for a professional with these required skills: MS in a scientific/technical discipline such as chemistry or chemical engineering with 3 or more years of experience, or BS with at least 5 years of experience.
Education to a degree level and qualification in Técnico Superior en Prevención de Riesgos Laborales (in the 3 specialties) following Spanish Health and Safety regulations.
Relevant experience complying with local Health and Safety legislation.
Knowledge of essential regulatory guidelines, worldwide policies, and procedures.
Previous experience in risk management, including root cause analysis, corrective and preventive actions (CAPA).
Demonstrated experience managing and engaging senior stakeholders, peers, and teams.
Experience working and influencing in a cross-functional, matrix environment.
Proven ability to manage a broad variety of projects and priorities.
Experience in problem solving and issues resolution.
High degree of communication and influencing skills.
Preferred Experience: A broad scientific/pharmaceutical industry background.
Demonstrated experience on Data Integrity principles (ALCOA) and Document Management Systems - DMS.
Offered: Immediate incorporation into a multinational group with strong growth.
Good work environment, career plan, etc.
Salary: Negotiable according to experience, between 45-50k € gross per year.
Working hours: From 7:30 to 17:00 (Monday to Thursday) and from 7:30 to 13:45 (Friday)