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Project Manager

Date Posted: May 17, 2024

Job Description

As a Project Manager for Pharmaceuticals projects in the France, you will be responsible for overseeing the planning, execution, and delivery of various pharmaceutical projects from initiation to completion. You will collaborate with cross-functional teams including R&D, Manufacturing, Quality Assurance, Regulatory Affairs, and Supply Chain to ensure projects are completed on time, within budget, and in compliance with regulatory standards. Your strong leadership, communication, and organizational skills will be essential in driving project success.

Key Responsibilities

  • Lead and manage pharmaceutical projects from initiation to completion, ensuring adherence to project scope, timeline, and budget.
  • Develop and maintain project plans, timelines, and budgets, and regularly communicate project status updates to stakeholders.
  • Coordinate cross-functional project teams, including R&D, Manufacturing, Quality Assurance, Regulatory Affairs, and Supply Chain, to ensure alignment and collaboration throughout the project lifecycle.
  • Identify and mitigate project risks and issues, and implement corrective actions as needed to ensure project success.
  • Ensure compliance with regulatory standards and industry best practices throughout the project lifecycle.
  • Foster a culture of continuous improvement and innovation within the project team to drive efficiency and effectiveness.
  • Provide leadership, guidance, and support to project team members, fostering a collaborative and high-performing team environment.

Required Qualifications and Skills

  • Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree (e.g., Master’s, MBA, PMP certification) preferred.
  • Minimum of 5 years of experience in project management within the pharmaceutical industry, with a proven track record of successfully managing complex pharmaceutical projects.
  • Strong understanding of pharmaceutical development, manufacturing, quality assurance, and regulatory requirements.
  • Excellent leadership, communication, and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and stakeholders.
  • Proven ability to manage multiple projects simultaneously, prioritize tasks, and meet deadlines in a fast-paced environment.
  • Strong problem-solving and decision-making skills, with the ability to identify and resolve project issues and risks.
  • Experience working in a GMP-regulated environment and knowledge of regulatory requirements (e.g., FDA, EMA) for pharmaceutical products.
  • Fluency in English; proficiency in French is a plus.

If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.

Reference no.: 122-4948-2918-NW

Registration no.: 968446516E

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