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Validation Specialist (BioTech equipment)

Title : Validation Specialist (BioTech equipment) profile
Sector : Engineering & Technical
Scientific & Laboratory
Location : Nationwide
Reference : CW120591
Contact : Conor Twomey
Office : Shannon
Tel : +353 21 4297422
Email : ctwomey@careerwise.ie

Job Description

QA VALIDATION SPECIALIST required by CareerWise Recruitment for our multinational Biotech client in the mid-west. The QA VALIDATION SPECIALIST completes Document Preparation and Field Execution activities for the initial Qualification and Validation of the BioTech facility. The Role
  • Drive User Requirement Spec (URS) and SIA (System Impact Assessment) approval.
  • Generate Equipment Qualification Assessments (EQAs) and subsequent IQ, OQ and where necessary PQ, Cleaning Validation protocols; drive approval of same.
  • Execute IQ, OQ and where necessary PQ protocols and drive post-approval of same.
  • Interface with Commissioning and Process Sciences teams.
  • Support CIP and SIP validation programs as necessary.
  • Support Management in Project delivery.

Requirements:
  • Degree qualified in relevant Engineering or Science discipline
  • 3+ yrs experience
  • Proven BioTech experience in the given area
  • Experience in Document Preparation and Execution
  • Experience in major start-ups where construction, C&Q, PQ may be concurrent activities.
  • Good technical knowledge of BioTech equipment and the concepts of BioTech manufacturing.
  • Have Troubleshooting and analytical mindset.

Established in 1999, CareerWise Recruitment is recognised by many of the major indigenous and multinationals companies to be one of Irelands leading specialist Technical and Executive Recruitment firms. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway and Dublin. Supporting Business Demands & Growth since 1999 CareerWise Recruitment accepts that you do not wish your CV to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will be respected at all times.


 

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Careerwise Recruitment



Validation Specialist (BioTech equipment)

Title : Validation Specialist (BioTech equipment) profile
Sector : Engineering & Technical
Scientific & Laboratory
Location : Nationwide
Reference : CW120591
Contact : Conor Twomey
Office : Shannon
Tel : +353 21 4297422
Email : ctwomey@careerwise.ie

Job Description

QA VALIDATION SPECIALIST required by CareerWise Recruitment for our multinational Biotech client in the mid-west. The QA VALIDATION SPECIALIST completes Document Preparation and Field Execution activities for the initial Qualification and Validation of the BioTech facility. The Role
  • Drive User Requirement Spec (URS) and SIA (System Impact Assessment) approval.
  • Generate Equipment Qualification Assessments (EQAs) and subsequent IQ, OQ and where necessary PQ, Cleaning Validation protocols; drive approval of same.
  • Execute IQ, OQ and where necessary PQ protocols and drive post-approval of same.
  • Interface with Commissioning and Process Sciences teams.
  • Support CIP and SIP validation programs as necessary.
  • Support Management in Project delivery.

Requirements:
  • Degree qualified in relevant Engineering or Science discipline
  • 3+ yrs experience
  • Proven BioTech experience in the given area
  • Experience in Document Preparation and Execution
  • Experience in major start-ups where construction, C&Q, PQ may be concurrent activities.
  • Good technical knowledge of BioTech equipment and the concepts of BioTech manufacturing.
  • Have Troubleshooting and analytical mindset.

Established in 1999, CareerWise Recruitment is recognised by many of the major indigenous and multinationals companies to be one of Irelands leading specialist Technical and Executive Recruitment firms. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway and Dublin. Supporting Business Demands & Growth since 1999 CareerWise Recruitment accepts that you do not wish your CV to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will be respected at all times.


 

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