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Project Manager – Greenville, SC

Responsibilities

• The Project Manager coordinates and manages defined projects that support pharmaceutical product development, product transfer projects, and new product commercialization/launch activities.
• Responsible for planning and executing assigned projects, associated budgets, timelines and other project-specific deliverables within the scope of the initiative/project.
• Assess risks, develops mitigation plans and lead regular team meetings working across functionally with Manufacturing, Quality Assurance, Quality Control, Validation, and Regulatory departments.
• Responsible for elevating unresolved issues, including timely communication to department management and engages and Governances that drive resolution as needed.
• Responsible for development of key processes and systems that are in compliance with cGMPs, regulatory standards, and company policies and procedures to organize/track and communicate initiative status to multi-disciplinary teams.
• Relocation provided.

Requirements

• The Project Manager will have a BS degree with an engineering or science major.
• 5 years of experience in the pharmaceutical industry. Packaging experience a plus.
• Project Management Professional Certification (PMP) is a strong plus.
• Experience in liquid manufacturing preferred.
• New product launch experience required.
• Must be legally authorized to work in the U.S. and have a stable work history. Sponsorship is not available.

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