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QC Data Reviewer

Employer
Thornshaw Recruitment
Location
Westmeath, Leinster (IE)
Salary
Negotiable depending on experience
Start date
14 Jun 2021
Closing date
14 Jul 2021

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Discipline
Quality, GMP, QA / QC, QC Analyst
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

My client, a global CRO company based in Co. Westmeath, is looking for an QC Data Reviewer/ Analytical Reviewer to join their team.

This is a full-time permanent position with options of half working from home and working on site. As a QC Reviewer you will monitor the quality of laboratory data and reports.  


Summarized Purpose: 
Monitors the quality of laboratory data and reports. Reviews chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs). Evaluates data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP).

Essential Functions:  

  • Evaluates laboratory data for compliance with analytical methods and SOPs.
  • Reviews sample results for completeness and accurate representation of the data and report findings.
  • Communicates with laboratory staff to proactively address the quality of laboratory documentation.
  • Prepares QC statements noting deficiencies with the analytical data set or notebooks. Reports deficiencies to the project leader for correction.
  • Trains new QC Reviewers and laboratory staff.
  • Conducts SOP review and writing. Conducts consultations for quality records.
  • Performs other duties as assigned.

Job Qualification

Education and Experience:  

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification   
  • Min. 2 years experience - laboratory analytical experience utilising chemistry analytical techniques and reviewing data.
  • Experience in chromatography 

Knowledge, Skills and Abilities: 

  • Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP  
  • Thorough knowledge of chromatography and divisional SOPs  
  • Strong technical knowledge including an understanding of laboratory procedures, methodology and standards  
  • Ability to independently review laboratory reports and analytical methods  
  • Ability to deal with multiple and changing priorities  
  • Ability to provide clear and concise feedback and/or documentation of results  

For a full Job Spec and to apply for this role please call Zoe on +353 1 2784671 or e-mail zhamilton@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

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For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
Website

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