Overview About Us: Inova is a premier pharmaceutical consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team of experts specializes in guiding pharma companies through complex regulatory landscapes and ensuring the highest standards of product quality and safety.
Job Description: We are seeking a skilled and proactive Site Engineer to join our team at Inova. The successful candidate will play a crucial role in overseeing and managing on-site activities for our pharmaceutical and biotech clients. This role involves ensuring the successful execution of engineering projects, maintaining safety standards, and ensuring that all work is completed in accordance with regulatory and quality requirements. This is a unique opportunity to contribute to the development of critical infrastructure in the pharma and biotech industries.
Responsibilities On-Site Project Management: Oversee and manage all on-site activities, ensuring that projects are completed on time, within scope, and budget, while meeting the required quality standards.
Technical Oversight: Provide technical guidance and support during the installation, commissioning, and validation of systems and equipment in pharmaceutical and biotech facilities.
Regulatory Compliance: Ensure all site activities comply with relevant industry standards and regulatory requirements, including GMP, FDA, and EMA guidelines.
Quality Assurance: Collaborate with quality assurance teams to ensure that all work is conducted according to established protocols and quality standards.
Safety Management: Implement and enforce safety protocols to maintain a safe working environment for all on-site personnel.
Stakeholder Communication: Serve as the primary on-site contact for clients, contractors, and other stakeholders, ensuring clear and effective communication throughout the project lifecycle.
Documentation: Maintain accurate and up-to-date documentation of all on-site activities, including progress reports, safety logs, and project records.
Problem Solving: Quickly address and resolve any issues that arise during on-site work, ensuring minimal disruption to project timelines.
Qualifications Bachelor’s or Master’s degree in Engineering (Mechanical, Electrical, Chemical, or related field).
3+ years of experience in a site engineering role, preferably within the pharmaceutical or biotech industries.
Hands-on experience managing site operations, including installation and commissioning of equipment in a regulated environment.
Strong understanding of GMP, FDA, and EMA regulations.
Experience with the installation and validation of pharmaceutical and biotech systems.
Proficiency in reading and interpreting engineering drawings and specifications.
Strong leadership and organizational skills.
Excellent problem-solving abilities and attention to detail.
Effective communication and interpersonal skills for managing on-site teams and interacting with clients.
Proficiency in English is required; additional languages, especially French or German, are a plus.
We Offer A competitive salary and benefits package.
Opportunities for professional growth and development.
A collaborative and inclusive work environment.
Participation in cutting-edge projects in the pharma industry.
How to Apply Interested candidates are invited to submit their CV via this form. Please include references and any relevant project details in your application.
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