Manager Validation & Projects – QTC Recruitment – Leiden

  • Leiden

QTC Recruitment

jobid=A.0.157

For one of our partners on the Leiden BioScience park, we are looking for a Manager Validation & Projects. This role offers a dynamic and challenging position within a GMP-regulated manufacturing environment. You will be responsible for leading the Validation and Projects teams and play a crucial role in successfully executing both internal and external projects. Are you a driven people leader with a talent for coordination and problem-solving? Then this might be interesting for you!

About your role

As Manager Projects & Validation, you are at the centre of executing complex projects and validation activities. You will work closely with various teams and stakeholders to ensure that projects are delivered on time, within scope, and according to quality standards. Your responsibilities include:

  • Leading multidisciplinary teams and coordinating project activities.
  • Developing and managing milestone-based project plans and deliverables.
  • Monitoring progress and addressing bottlenecks to ensure timely project completion.
  • Analysing process performance and initiating improvements in quality and productivity.
  • Planning, executing, and supervising validation activities in accordance with the System Development Life Cycle (SDLC).
  • Preparing and managing validation documentation, including risk assessments, user requirements, SOPs, and test protocols (IQ, OQ).
  • Acting as the key liaison between operations and project teams, ensuring clear communication with stakeholders.
  • Managing team activities, including setting objectives, performance evaluations, and recruitment.
  • Ensuring compliance with GMP and quality system requirements.

What you bring

With a A BSc or MSc in project management or equivalent through experience & at least 5 years of experience in a (project) management role, the right candidates brings along:

  • Experience in the life sciences sector (biotechnology or related) is highly preferred.
  • Knowledge of GMP regulations within the pharmaceutical industry.
  • Excellent communication skills and the ability to collaborate effectively within a matrix organisation.
  • Critical thinking and problem-solving abilities.
  • Strong technical writing skills and proficiency in English (German/Dutch is a plus).

What the organisation offers

Besides allowing yourself to positively develop a team of 8FTE, the role offers the following benefits:

  • A competitive salary aligned with your experience and responsibilities.
  • A 13th-month salary.
  • 30 leave days.
  • A stable pension plan and company contribution to your health insurance.
  • A role within a dynamic and growing biopharmaceutical organisation with an inspiring work environment.
  • The opportunity to make an impact in a company dedicated to improving lives.

If you are interested in this or a similar position, feel free to reach out to us.

Achilleas Farmakis

Recruiter | Biotechnology & Pharmaceuticals

+316 83 16 56 35

a.farmakis@qtcrecruitment.com

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