Project Manager with strong experience in Life Science (Pharma Industry)

Cagents; Pistoia; In loco; EUR 45.000 - 70.000; Tempo pieno

Descrizione del lavoro

A life sciences consulting firm is seeking a Project Manager in Pistoia, Italy, with strong experience in the pharmaceutical industry. The role requires at least 4 years in QA or Validation, expertise in project management, and knowledge of cGMP regulations. The ideal candidate will manage project scopes, submit reports, and perform safety assessments in a full-time capacity.

Competenze

• 4+ years of experience in the pharmaceutical sector, specifically in QA, Validation, or Commissioning.
• Experience in project management.
• Knowledge of cGMP and regulatory requirements.

Mansioni

• Manage scope of work as defined in proposals or contracts.
• Submit monthly status reports to clients and stakeholders.
• Perform project safety assessments.

Conoscenze

Pharmaceutical experience

Project management tools

Client needs interpretation

Regulatory knowledge (cGMP)

Formazione

Bachelor’s degree in Business or Life Sciences

Descrizione del lavoro

Project Manager with strong experience in Life Science (Pharma Industry) Italy / South Europe / Full Time

CAI Overview: Are You Ready?

CAI is a professional services company established in 1996, with nearly 800 employees worldwide. We serve the Life Sciences and Mission Critical industries by delivering critical solutions in high-stakes environments, ensuring operational readiness and top performance through rigorous processes and elite expertise developed over 30 years.

Our purpose is to be the trusted solution for our clients, helping them build a better working world and improve the human experience.

We are committed to our Foundational Principles :

• Act with integrity
• Serve each other
• Serve society
• Work for our future

At CAI, we strive for excellence, pushing boundaries and redefining industry standards. We operate at the intersection of wisdom, technology, and humanity, with operational readiness as our way of life. We are dedicated to continuous improvement through effort, precision, and innovation.

Key Responsibilities :

• Require at least 4 years of experience in the pharmaceutical sector, specifically in QA, Validation, or Commissioning.
• Knowledge of cGMP and regulatory requirements
• Experience with project management tools
• Ability to interpret client needs, assess requirements, and identify solutions for non-standard requests
• Collaborate to facilitate client alignment and best practices
• Manage scope of work as defined in proposals or contracts, initiating scope changes as needed
• Perform project safety assessments
• Submit monthly status reports to clients and stakeholders

Qualifications :

• Bachelor’s degree in Business, Life Sciences, or related field; advanced degrees preferred
• 4+ years of experience in professional services, consulting, or life sciences
• Relevant experience with specific systems, processes, or industry types

Leadership Competencies include :

• Business growth strategies
• Applying commercial insights
• Customer focus
• Execution leadership
• Influencing and engaging others
• Building talent
• Achieving results with people
• Leading courageously and safely

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