Science, Pharmaceutical & Food

Process Validation Technical Specialist

  • Contract
  • Remote
  • Dublin North
  • 41937653

 

The role:

PE Global is currently recruiting for a Senior Process Validation Technical Specialist on behalf of our client based in Dublin. This is an initial 12-month contract role.

 

Description:

  • The Process Validation Technical Specialist will be responsible for developing Validation and Technical Standards and Guidelines for Process validation and technical transfer programs across the internal and external manufacturing network.
  • This individual will be a part of the Global Technical Operations team and will report to the Director of Validation and Technical Standards.
  • Primary responsibilities include developing and maintaining Process Validation, continued process verification and other technical standards. This will ensure that technical guidelines are fit for purpose across multiple modalities and are updated as new modalities are introduced to the pipeline.
  • The role will also support the development of a Knowledge Management framework for the Global Technical Operations department
  • The role will support internal and external sites as they build and execute Process validation and tech transfer strategy to support the product pipeline

 

Responsibilities:

  • Develop and support the implementation of scientifically sound, fit for purpose standards and procedures for process validation and other technical procedures based on current regulations, industry standards and industry practices.
  • Deliver associated training to colleagues.
  • Support the implementation of innovative and efficient approaches to validation and technical transfer by internal and external sites incorporating science and risk-based approach.
  • Support the development and implementation of process validation plans and other validation documentation in collaboration with the validation and technical SME network.
  • Build strong cross functional working relationships with stakeholders (Quality, Development, Technical Services and CMOs) to ensure high quality deliverables meeting cGMP and validation requirements.

 

Education and Experience:

  • Minimum Bachelors’ degree in a scientific discipline (Biology, Biochemistry, Biotechnology, Chemistry), or related field.
  • A minimum of 6-8 years’ experience in the biopharmaceutical or pharmaceutical industry (Process Validation, Technical Services or Quality).
  • A minimum of 6 years’ direct experience in cGMP Process validation / technical transfer activities.
  • Extensive knowledge of Process Validation regulations, current process validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations.
  • Excellent technical writing skills
  • Experience of biopharmaceutical Bulk Drug Substance (BDS) manufacturing and aseptic fill finish.
  • Demonstrated active participation in industry and regulatory forums shaping validation practices and strategy.
  • Strong track record of working in a global and matrix environment and working cross functionally 

 

 

Interested candidates should submit an updated CV.

 

Please click the link below to apply, call Kellie on 0214297900 or alternatively send an up to date CV to kellie.hackett@peglobal.net

 

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

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