Validation Specialist

  • Zoetermeer
  • 3000.00 - 4500.00
  • 32-40 hours
  • Bachelor degree

Client

Our client is a consultancy in the food and pharmaceutical industry.

Client

Our client is a consultancy in the food and pharmaceutical industry. They participate in very attractive projects for experienced engineers in the pharmaceutical industry. They offer challenging, varied projects with ample opportunities for personal contributions and development.

Requirements

  • Minimal a Bachelor education
  • At least 10 years relevant work experience in QA.
  • Up to date GMP, FDA, IGJ knowledge and experience
  • Validation, qualification and automation experience
  • Experience in Biologicals
  • Experience in computed system validation (CSV) is a pre
  • Fluent in English, preferably Dutch speaking/understanding

What do you get?

  • Pension entitlement as from day one
  • Collective WGA / WIA insurance
  • NBBU / ABU collective labor agreement
  • 25 holidays days
  • 8,33% holiday allowance
  • 100% payment in case of illness after one waiting day
  • Travel allowance

Duties

  • Reviews and approves technical reports and other sources of information to ensure that validations and procedures are consistent with current industry, regulatory requirements, and current technology.
  • Ensures that validation, qualification and other life cycle activities are consistent with company validation policies and procedures and federal regulations.
  • Proceeds according to the company's quality policy in all business activities with providers and customers within and outside the company.
  • Evaluates technical problems and provides recommendations for corrective actions.
  • Represents Quality Assurance department in project teams.
  • Participates in company meetings related to changes in processes, process improvements, provide suggestions, and so on.
  • Provides coaching and training and guidance on aspects of validations and qualifications.
  • Provides support to internal and external customers of site quality in the execution of procedure and policy requirements.
  • Acts as a major contact for validation issues during regulatory and third party audits.
  • Works independently on implementing projects.
. Works on several projects in parallel.
  • Main focus areas are construction, utility and equipment introduction / software related to manufacturing.

TAGCLOUD

Sander Pupella

Interested

Send your resume to sander@tailorminds.com referring to job id (763)

More information?

Please contact Sander Pupella working at our office in Zoetermeer, phone number +31 6-13140754

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