Role Purpose:

  • A fantastic opportunity has arisen for a Quality Validation Engineer to join our client’s new manufacturing facility in Co. Kilkenny.
  • In the role of Quality Validation Engineer, you will be responsible for creating and implementing the company validation program.
  • Creating and maintaining validation documentation for new and existing systems and processes subject to design control.
  • You will also ensure that validation activities are implemented for systems and processes used to manufacture, control and store intermediates and finished products to requirements and standards as listed in the current Quality Systems Manual.
  • You will also have the opportunity to travel to vendor locations for training in Europe or the US.

Core Duties and Responsibilities:

  • The development and maintenance of Quality System procedures.
  • Ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance.
  • Monitoring and maintaining the quality and compliance status of associated quality records.
  • Maintaining the quality and compliance status of associated Procedures, work instructions and training materials.
  • Presenting and communicating status, report metrics, identify trends potential issues, improvement initiatives, as applicable.
  • The review and approval of validation documentation in accordance with divisional policies.
  • Basic understanding of design controls and design transfer.

Education & Qualifications Required:

  • Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
  • Minimum 4 years in the Engineering/Manufacturing/ Scientific field.
  • 5-6 years working knowledge of process, equipment, facilities and or software validation either within Quality or Engineering departments
  • Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations.

Please note, we do not require agency assistance with this role.


Apply Now

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Full Name*
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
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Role Details:

Job Title: Quality Validation Engineer
Location: Kilkenny
Type: Permanent
Date: July, 2024
Image of recruitment specialist

Discuss with:

Ruth Holland
recruitment@prochem.ie
Recruitment Specialist
on +353 56 779 0100
Share:

Role Details:

Job Title: Quality Validation Engineer
Location: Kilkenny
Type: Permanent
Date: July, 2024
Image of recruitment specialist

Discuss with:

Ruth Holland

recruitment@prochem.ie

Recruitment Specialist

on +353 56 779 0100

Share:

Role Purpose:

  • A fantastic opportunity has arisen for a Quality Validation Engineer to join our client’s new manufacturing facility in Co. Kilkenny.
  • In the role of Quality Validation Engineer, you will be responsible for creating and implementing the company validation program.
  • Creating and maintaining validation documentation for new and existing systems and processes subject to design control.
  • You will also ensure that validation activities are implemented for systems and processes used to manufacture, control and store intermediates and finished products to requirements and standards as listed in the current Quality Systems Manual.
  • You will also have the opportunity to travel to vendor locations for training in Europe or the US.

Core Duties and Responsibilities:

  • The development and maintenance of Quality System procedures.
  • Ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance.
  • Monitoring and maintaining the quality and compliance status of associated quality records.
  • Maintaining the quality and compliance status of associated Procedures, work instructions and training materials.
  • Presenting and communicating status, report metrics, identify trends potential issues, improvement initiatives, as applicable.
  • The review and approval of validation documentation in accordance with divisional policies.
  • Basic understanding of design controls and design transfer.

Education & Qualifications Required:

  • Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
  • Minimum 4 years in the Engineering/Manufacturing/ Scientific field.
  • 5-6 years working knowledge of process, equipment, facilities and or software validation either within Quality or Engineering departments
  • Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations.

Please note, we do not require agency assistance with this role.

Image of recruitment specialist

Discuss with:

Ruth Holland
recruitment@prochem.ie
Recruitment Specialist
on +353 56 779 0100
Share:

Apply Now

"*" indicates required fields

Full Name*
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
Accepted file types: pdf, docx, odt, doc, txt, Max. file size: 32 MB.
Hidden
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