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Senior CQV Engineer Pharma

  • Lieu:

    Hoofddorp, Pays-Bas

  • Contact:

    Sejla Ramic

  • Type de poste:

    Contract

  • Téléphone de contact:

    +31 (0)20 406 97 50

  • Secteurs d’activité:

    Pharmaceutical

  • Contact E-mail:

    sejla_ramic@oxfordcorp.com

Our client operates in a highly regulated manufacturing environment where product quality, compliance, and operational excellence are essential. To support ongoing technical projects and system lifecycle activities, they are looking for an experienced quality professional with strong expertise in validation and engineering-related quality processes.

Job Description
As a Senior Quality Engineer focused on commissioning, qualification, and validation activities, you will play a key role in safeguarding compliance across manufacturing and engineering initiatives. You will act as a quality partner for technical projects, ensuring systems and process changes are designed, implemented, and maintained in line with regulatory expectations. The role combines independent execution of routine quality tasks with leadership and judgment on complex validation topics, requiring both technical knowledge and cross‑functional collaboration.

Responsibilities

  • Provide quality guidance and oversight for validation and engineering projects
  • Support the introduction of new equipment and systems by offering technical quality expertise
  • Define and apply risk‑based validation approaches for changes affecting operations
  • Review, assess, and approve validation documentation for initial, modified, and periodic activities
  • Contribute to improvements in processes and quality systems across departments
  • Ensure adherence to GMP and GLP requirements through active quality programs
  • Identify deviations, assess their impact, and support resolution of complex quality issues
  • Collaborate with operational teams to support inspections, audits, and process monitoring
  • Assist with internal or external audits when needed


Requirements

  • Bachelor's degree (BSc) in a relevant scientific or engineering discipline
  • Solid experience applying quality engineering principles and industry standards
  • Strong written and verbal communication skills, including technical documentation
  • Ability to work independently on routine tasks and adapt to new assignments
  • Experience working in regulated manufacturing or laboratory environments
  • Preferred: familiarity with Six Sigma / DMAIC methodologies
  • Preferred: experience with risk assessment tools such as FMEA or HACCP


Benefits

  • Start via Oxford Global Resources for the first year
  • Estimated salary: €6000 gross per month
  • Region: Amsterdam area
  • Working hours: Monday to Friday, standard office hours (09:00-17:00)
  • Additional benefits: exposure to complex technical projects, collaboration with multidisciplinary teams, and opportunities to further develop validation and quality expertise
  • Vacancy number: 27191