Project Engineer

Company:  Meet
Location: Wrexham
Closing Date: 04/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Project Engineer About the Company We are a dynamic and rapidly growing specialty-driven biopharmaceutical company focused on innovation and specialty care. Our commitment to improving patient outcomes drives everything we do, and we believe our employees are our most valuable asset. We seek bold, agile, and entrepreneurial individuals to join our mission of making a positive impact on people’s lives. Position Overview Are you an ambitious engineer passionate about delivering innovative projects in a fast-paced environment? We are looking for a Project Engineer to support key work packages as part of our new facility development and play a pivotal role in driving efficiency in our capital investment programs. Key Responsibilities Engineering Leadership: Provide technical leadership within your engineering discipline (process, mechanical, or electrical). Ensure full compliance with internal and external standards, practices, and regulatory requirements. Conduct technical evaluations to identify optimal engineering solutions. Lead design reviews and develop key technical documents (e.g., User Requirement Specifications, Technical Specifications). Project Management: Manage project work packages, ensuring delivery within scope, time, and budget constraints. Develop detailed project plans aligned with business objectives. Collaboration and Coordination: Work collaboratively within the project engineering team and communicate effectively with cross-functional stakeholders. Liaise with vendors to oversee design reviews, fabrication, installation, and testing activities. Commissioning and Qualification: Support commissioning and qualification activities. Ensure smooth handover of completed projects to relevant stakeholders. Innovation and Continuous Improvement: Proactively identify innovative solutions and drive process improvements. Perform root cause analysis to prevent recurring issues. Quality and Compliance: Ensure compliance with GMP regulations for sterile product manufacturing. Develop and implement Quality Risk Assessments to mitigate project risks. Safety and Environmental Management: Take ownership of safety and environmental considerations for new systems and projects. Ensure safe equipment startup, shutdown, and adherence to job control practices. Qualifications and Experience Degree in Chemical Engineering, Mechanical Engineering, or equivalent. Professional affiliation with IChemE, IMechE, ISPE, or similar is desirable. Proven experience in project management within a regulated, cGMP environment. Strong understanding of engineering design processes. Experience with pharmaceutical manufacturing process equipment and utility systems is preferred. Why Join Us? Opportunity to contribute to cutting-edge projects within a rapidly growing biopharmaceutical company. Work on a major multi-million-pound investment to expand our manufacturing capabilities. A collaborative and inclusive work environment, with a focus on personal and professional growth. Competitive salary, annual bonus, generous pension scheme, wellness benefits, and more. Commitment to sustainability and diversity, with recognition as one of the best workplaces for women and well-being. Make a direct impact on people’s lives and grow your career with us
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