Pharmaceutical Project Manager

Description:

The work scope will include operations excellence, continuous improvement projects, and capacity expansion projects in support of commercial products. This role will work with project management and subject matter experts across multiple sites including Manufacturing, Operational Excellence, Supply Chain, MS&T, Quality Assurance, Quality Control, Process Development, CMC, TT lead, TCT lead, Global Engineering, Facilities Engineering, PMO, IT, EHS, Finance, Regulatory, and Clinical and Commercial Operations.

Required Knowledge, Skills, and Abilities:

• Ability to work independently
• Ability to matrix manage cross-functional teams
• Must be competent in Project Management tools and methodologies
• Excellent organizational and time management skills
• Experience with regulated GMP environment for manufacturing (Biologics or Cell Therapy experience is a plus).
• Strong analytical, problem-solving, and critical thinking skills
• High attention to detail skills
• High organization skills with the ability to multi-task several objectives in parallel
• People and project management skills
• Advanced proficiency in MS Office applications
• Proficient written and verbal communication skills
• Ability to develop and provide training on various functions

Education and Experience:

• Bachelor’s degree required in Science or Engineering
• 5+ years of relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment.
• PMP certification is strongly preferred.
• Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization.