GMP Validation Engineer for Manufacturing & Compliance

Ferring Holding SA

Roseville (MN)

Presencial

USD 77.000 - 110.000

Tempo integral

Há 10 dias

Uma candidatura completa em um minuto

Currículo e carta de apresentação personalizados, prontos para serem enviados.

Passe pelos filtros ATS

Benefícios oferecidos por esta vaga

Comprehensive healthcare (medical, den
401k plan with company match
Vacation time and holidays
Parental leave
Wellness benefits
Tuition reimbursement

Resumo da vaga

Ferring is seeking a Validation Engineer in Roseville, Minnesota to prepare and execute commissioning, qualification, and validation activities for processes, materials, equipment, cleaning, and computerized systems.

This role supports GMP manufacturing, performs risk assessments, generates documentation, and collaborates with project teams to ensure compliant, timely validation. Competitive salary range and benefits are offered.

Qualificações

  • Bachelor’s degree in engineering or equivalent.
  • 3–5 years qualification/validation experience.
  • Experience in GMP manufacturing preferred.
  • Proficiency with MS Office tools.

Responsabilidades

  • Support validation activities in a cGMP regulated manufacturing environment.
  • Prepare, review, and execute commissioning, qualification and validation documents.
  • Assist in design qualifications and risk assessments.
  • Support validation projects including new or transferred processes and cleaning validations.
  • Design and execute pre-validation studies.
  • Assist in troubleshooting process issues and root cause investigations.
  • Prepare/change controls, CAPAs, and investigations.

Conhecimentos

GMP experience
Process validation
Computerized system
Risk assessment
MS Office

Formação

Bachelor’s degree in engineering or relevant field

Ferramentas

Microsoft Office

Descrição da vaga

Ferring is seeking a Validation Engineer in Roseville, Minnesota to prepare and execute commissioning, qualification, and validation activities for processes, materials, equipment, cleaning, and computerized systems.

This role supports GMP manufacturing, performs risk assessments, generates documentation, and collaborates with project teams to ensure compliant, timely validation. Competitive salary range and benefits are offered.

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