GMP Project Manager

About the role

The role of GMP Project Manager involves overseeing the implementation and compliance of Good Manufacturing Practices within a pharmaceutical company. Key responsibilities include managing project timelines, ensuring regulatory compliance, and coordinating with cross-functional teams.

Responsibilities

• Oversee the implementation and compliance of GMP standards
• Manage project timelines and budgets
• Ensure regulatory compliance and audit readiness
• Coordinate with R&D, manufacturing, quality control, and supply chain teams
• Develop and maintain project documentation
• Conduct regular status meetings with stakeholders
• Prepare and present project progress reports

Requirements

• Bachelor’s degree in a relevant field (e.g., Biotechnology, Chemistry)
• Minimum 5 years of experience in pharmaceutical operations or related field
• Proven experience in project management and leadership
• Strong understanding of GMP regulations and industry best practices
• Excellent organizational and problem-solving skills
• Ability to work independently and in a team environment
• Proficient in Microsoft Office Suite

Qualifications

• Knowledge of cGMP guidelines and FDA regulations
• Experience with project management tools and software
• Strong verbal and written communication skills
• Ability to manage multiple projects simultaneously

Skills

• Project Management
• Regulatory Compliance
• Team Leadership
• Documentation Management
• Communication Skills

Benefits

• Competitive salary package
• Flexible working hours
• Professional development opportunities
• Health insurance benefits
• Employee wellness programs

Pay

Salary range: $70,000 - $90,000 annually

Schedule

Full-time, Monday through Friday, 9:00 AM - 5:00 PM

Resources

For more information about the company and the role, visit our resources page.