Remote Senior Product Lifecycle Manager – Drug Development

ProPharma; Stockholms kommun; Hybrid; SEK 1,200,000 - 1,800,000; Full time

Job summary

ProPharma is seeking a Senior Consultant in Product Lifecycle Management to drive strategic plans for life-science clients. You will manage complex projects, lead cross-functional teams, and coordinate with finance and other departments to align with budgets and timelines.

The role offers exposure to diverse drug development programs, including GMP/ISO considerations, with a focus on delivering high-impact outcomes on a global scale. Hybrid work is available within Sweden.

Qualifications

• Must have 10–15 years in life-sciences
• Strong project leadership for drug development
• Experience with drug development and small molecule projects preferred
• Ability to develop proposals and present to clients
• Hands-on experience with remote CMO management
• Excellent analytical communication of complex issues

Responsibilities

• Manage complex manufacturing and transfer projects to timely decision points
• Lead projects within the Biological space
• Develop and execute project team strategy aligned with budget and timeline
• Maintain integrated project schedules for financial analyses and planning
• Oversee project team budgets and resources
• Communicate, document, and archive project activities
• Facilitate cross-functional meetings and decisions
• Identify and implement process improvements
• Support staffing to meet revenue and growth goals
• Perform other duties as assigned

Skills

Project management

English fluency

cGMP knowledge

ISO knowledge

Stakeholder management

Presentation skills

Remote/CMO management

Education

BSc or above in Life-sciences

Job description

ProPharma is seeking a Senior Consultant in Product Lifecycle Management to drive strategic plans for life-science clients. You will manage complex projects, lead cross-functional teams, and coordinate with finance and other departments to align with budgets and timelines.

The role offers exposure to diverse drug development programs, including GMP/ISO considerations, with a focus on delivering high-impact outcomes on a global scale. Hybrid work is available within Sweden.