Project Engineer at Ceva Sant Animale

Loudéac, Brittany, France -

Full Time

Start Date

Immediate

Expiry Date

05 Jul, 26

Salary

0.0

Posted On

06 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, GMP, Process Engineering, Regulatory Compliance, Risk Assessment, Validation, Lean, Six Sigma, AutoCAD, CMMS, MES, Technical Documentation, Supplier Management, Industrial Equipment, Quality Assurance, Automation

Industry

Pharmaceutical Manufacturing

Description

Project Engineer The success of a company depends on the passionate people we partner with. Together, let's share our talents. As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet. We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife. Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach. As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team. Your missions : Ceva Santé Animale is seeking a Project Engineer for a permanent position (CDI) based in Loudéac, Brittany. As a Project Engineer, you are responsible for planning, coordinating, and managing industrial, technical, or cross-functional projects within the production site. You ensure that quality, cost, timeline, and regulatory compliance objectives are met in a highly regulated environment. As part of Good Manufacturing Practices (GMP) and Ceva’s policy, you optimize the reliability of all production operations on the site in terms of quality, cost, and lead time, focusing on the development of industrial equipment and best practices in quality and safety. You are responsible for executing a portion of engineering projects valued at over €2 million, applying project management methodologies. =>Project Management Define the scope, resources, milestones, and timelines of projects. Develop risk assessments, budgets, and action plans. Lead project meetings and coordinate internal and external teams. Monitor key indicators: progress, costs, risks, quality. Prepare and present reports to management. =>Equipment Development, Installation and Qualification Manage projects related to the acquisition, modification, or modernization of production or laboratory equipment. Oversee FAT and SAT phases (according to GMP processes). Support production start-up and ramp-up phases. Coordinate technical validations (process, cleaning, software, utilities). =>Regulatory Compliance & Quality Ensure that projects comply with regulatory requirements, GMP, and Feed regulations. Participate in drafting and updating technical documents (URS, SOPs, validation protocols, reports, change controls). Collaborate with Quality Assurance and Regulatory Affairs during audits and inspections. =>Continuous Improvement Identify opportunities for optimizing processes, equipment, or workflows (Lean, 5S, Six Sigma, FMEA). Propose and implement innovative technical solutions to improve performance and reliability. Contribute to the digitalization of equipment or processes (MES, IoT, automation). =>Supplier Relations & Contract Management Write technical specifications. Select and manage suppliers, integrators, and subcontractors. Manage tenders and negotiate technical and financial aspects. Oversee contracts, schedules, and acceptance procedures. Your profile : You hold a general engineering degree or a specialized degree in process engineering, chemical engineering, biomedical engineering, mechanical engineering, automation, or an equivalent field (Master’s level). A specialization in the pharmaceutical or veterinary industry is a strong advantage. You have at least 3 years of experience independently managing multiple industrial projects. =>Technical Skills / Expertise Solid knowledge of regulated environments: GMP, ISO, GLP, HACCP (depending on the sector). Proficiency in project management (PMI, Prince2 certifications appreciated – Agile methods depending on context). Skills in qualification, validation, URS, and risk assessments. Knowledge of utilities: HVAC, purified water, clean steam, compressed air, etc. Understanding of manufacturing processes: solid and liquid forms, injectables, veterinary feed/medicine, vaccines… Proficiency in digital tools: Smartsheet, AutoCAD, CMMS or MES software. =>Soft Skills / Behavioural Competencies You ensure the reliability and accuracy of your work through the use of relevant indicators and a strong sense of responsibility. You demonstrate clarity, structure, and confidence in your communication, with strong summarizing skills. You are open to knowledge-sharing and feedback, in a continuous improvement mindset.

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Responsibilities

The Project Engineer is responsible for planning, coordinating, and managing industrial and technical projects within the production site to meet quality, cost, and timeline objectives. They oversee equipment development, installation, and qualification while ensuring strict adherence to regulatory compliance and Good Manufacturing Practices.