Senior Project Manager

Position Summary We are looking for a Senior Project Engineer who will be responsible for overseeing the planning, execution, and completion of projects. The ideal candidate will have a strong background in project management within the pharmaceutical industry, with a focus on capital projects related to manufacturing facilities, laboratories, and infrastructure. Duties & Responsibilities

• Lead end-to end project management, including initiation, planning, execution, monitoring and project closure. Ensure adherence to timelines, budgets, and quality standards.

• Collaborate with stakeholders such as engineering, manufacturing, and quality to define scope, objectives, and deliverables.

• Manage relationships with external vendors, contractors, and suppliers to ensure timely delivery of equipment, materials, and services.

• Develop comprehensive project plans and resource loaded schedules to ensure on-time implementation.

• Identify and mitigate project risks, proactively addressing issues to prevent delays or cost overruns.

• Develop and manage project budgets, allocate resources effectively, and track expenses to ensure financial objectives are met.

• Create project dashboards for monitoring progress and communicating risks.

• Build strong relationships with stakeholders and effectively communicate project updates and challenges.

• Conduct thorough project reviews to identify lessons learned and areas for continuous improvement.

• Promote a culture of continuous improvement throughout the site, fostering innovation and best practices. Required Qualifications

• Bachelor’s degree and 10 years of project management experience. PMP certification preferred.

• Continuously looking for opportunities to learn, build skills, and share knowledge with others.

• Proven experience with a focus on capital projects within the pharmaceutical industry.

• Strong understanding of pharmaceutical manufacturing processes and facilities.

• Must be versed in Project Management tools and must have knowledge of related disciplines.

• Experience working in cGMP environments that meet FDA, ICH guidelines, local regulations, and industry best practices. -

• Demonstrated ability to work in a fast-paced team environment, meet deadlines, and prioritize work. Start-up experience preferred.

• Proven track record of being self-motivated and capable of working with cross-functional teams while remaining positive towards project challenges. Preferred Qualifications

• Greenfield and startup experience strongly preferred.

• Engineering background and experience is a plus.

• PMP Certification.