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This role is ideal for someone with a background in the pharmaceutical or chemical industry who thrives on connecting departments, driving sustainability initiatives, and embedding environmental responsibility into everyday operations. **Your Role**\nAs a Sustainability Specialist, you will:* Support the implementation and continuous improvement of Hovione’s Sustainability Management System.\n* Lead and contribute to sustainability projects, including current initiatives such as **water saving and resource efficiency**.\n* Build bridges between departments to ensure alignment and engagement with sustainability goals.\n* Promote and ensure compliance with internal and external sustainability standards and regulations.\n* Monitor and report on sustainability performance indicators, identifying opportunities for improvement.\n* Support internal and external audits related to sustainability and environmental compliance.\n* Develop and deliver training and awareness programs to foster a culture of sustainability.\n* Collaborate with vendors, regulatory bodies, and internal stakeholders to ensure successful project execution.\n* Ensure all activities are conducted in alignment with GMP, HSE, and company policies.\n\n \n\n\nWe are looking to recruit a Candidate::\n**What You Bring*** University degree in Environmental Engineering, Sustainability, Industrial Engineering, or a related scientific field (mandatory).\n* Preferences: 3–5 years of experience in sustainability or environmental roles, preferably within the pharmaceutical or chemical industry.\n* Strong understanding of sustainability principles, environmental regulations, and management systems.\n* Experience in leading or supporting cross\\-functional projects and initiatives.\n* Excellent communication and stakeholder engagement skills.\n* Fluency in English (mandatory).\n* Proficiency in MS Office and other relevant digital tools.\n\n **Hovione is a proud Equal Opportunity Employer**\nInclusion and diversity are key to us. 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That is why we are **In it for life.**\nYou will be responsible to::\n* Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured;\n* Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports;\n* Prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following\\-up action plans as necessary;\n* Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits;\n* Periodic follow\\-up of ongoing deviations and Change Controls (PdAs) to assure timely closure of deviations and approval of PdAs, as appropriate;\n* Prepares SOPs, department IOPs, quality related reports and change control documents (PdAs) as required and appropriate;\n* Review process master documentation, revision of executed batch documentation and product specifications as required and appropriate;\n* Review regulatory documentation and co\\-ordination of site documentation to support regulatory requirements;\n* Authorize the usage of production equipment/utilities when qualification required.\n\n\nWe are looking to recruit a Candidate::\n* University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory);\n* Requires educational / training experience in Chemical environment (desirable);\n* Fluency in English is a requirement;\n* Computer literate with good working knowledge of the MS Office package;\n* Good documentation skills and attention to detail.\n\n **Hovione is a proud Equal Opportunity Employer** \n\nInclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity. ***Notice to Agencies and Search Firms Representatives*** \n\n*Hovione does not accept unsolicited résumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third\\-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral. 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António Caetano Bernardo 6B, 2670-457 Loures, Portugal","infoId":"6382272706867312","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Quality Assurance Trainee","content":"Join a Market Leader:\n\nHovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\\-patent drugs to market. \n\nOur people are the main asset for our continued success. 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