Job Description

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Quality Control Associate

Advertiser: CPR Pharma Services4.3 out of 54.3 overall rating (4 employee reviews) More jobs from this company

Job Information

Job Listing Date
12 Oct 2018
Location
Adelaide
Work Type
Part Time
Classification
Science & Technology, Quality Assurance & Control

Quality Control Associate

CPR Pharma Services (CPR) full-service Clinical Research Organisation with an international reputation for delivering high quality clinical trial results. We facilitate quality drug development by aligning our people, their skills and expertise in the pursuit of a healthier world.

The Opportunity

An opportunity has arisen for an experienced Quality Control Associate to join our bioanalytical team at CPR. Reporting to the Laboratory Operations Manager or delegate you will be responsible fore ensuring data produced can be deemed accurate and credible through a system of adequate QC. This role per a permanent part-time role working 3 days per week.

The Role

Your responsibilities will include: 

  • Identifying errors or non compliant practices in accordance with CPR Standard Operating Procedures
  • Identifying administrative/clerical errors in documentation
  • Raw Data checking
  • Quality control reviews of raw data against exported data
  • Formulae checks; sample code, names, data cross checks
  • Anomaly checks
  • Study file documentation reviews 
  • Communicating identified issues to Analysts and Study Directors as applicable
  • Working within CPR Quality Control Systems to improve GCLP compliance, meet Regulatory and CPRs standards.
  • Contributing to continuous improvement of the CPR laboratory through the author and review of Standard Operating Procedures.

About You

  • Successful completion of a relevant Bachelors Degree in Science, Pharmaceuticals or Chemistry
  • Extensive practical and theoretical expertise in bioanalytical techniques, development and troubleshooting
  • Proven ability to deliver tasks on time and with a high degree of accuracy
  • Proven ability to set priorities, analyse problems, formulate clear and effective solutions and co-ordinate a number of tasks simultaneously
  • Demonstrated initiative, trust and reliability and the ability to work unsupervised
  • High level of verbal and written communication skills in the English language
  • Intermediate skills in Microsoft Office Suite
  • Experience in the pharmaceutical industry or CRO environment (highly desirable)

To apply

  • To apply for this role please click on the 'apply for this job' link and submit your CV along with a cover letter outlining your skills and experience, please submit as one Microsoft Word document.
  • To be considered for this role you must be able to provide evidence of entitlements to work in Australia.
  • As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process.
  • For further information about CPR Pharma Services, please visit our website at http://www.cprservices.com.au

CPR Pharma Services is an equal opportunity employer

 

 

 

CPR Pharma Services (CPR) full-service Clinical Research Organisation with an international reputation for delivering high quality clinical trial results. We facilitate quality drug development by aligning our people, their skills and expertise in the pursuit of a healthier world.

The Opportunity

An opportunity has arisen for an experienced Quality Control Associate to join our bioanalytical team at CPR. Reporting to the Laboratory Operations Manager or delegate you will be responsible fore ensuring data produced can be deemed accurate and credible through a system of adequate QC. This role per a permanent part-time role working 3 days per week.

The Role

Your responsibilities will include: 

  • Identifying errors or non compliant practices in accordance with CPR Standard Operating Procedures
  • Identifying administrative/clerical errors in documentation
  • Raw Data checking
  • Quality control reviews of raw data against exported data
  • Formulae checks; sample code, names, data cross checks
  • Anomaly checks
  • Study file documentation reviews 
  • Communicating identified issues to Analysts and Study Directors as applicable
  • Working within CPR Quality Control Systems to improve GCLP compliance, meet Regulatory and CPRs standards.
  • Contributing to continuous improvement of the CPR laboratory through the author and review of Standard Operating Procedures.

About You

  • Successful completion of a relevant Bachelors Degree in Science, Pharmaceuticals or Chemistry
  • Extensive practical and theoretical expertise in bioanalytical techniques, development and troubleshooting
  • Proven ability to deliver tasks on time and with a high degree of accuracy
  • Proven ability to set priorities, analyse problems, formulate clear and effective solutions and co-ordinate a number of tasks simultaneously
  • Demonstrated initiative, trust and reliability and the ability to work unsupervised
  • High level of verbal and written communication skills in the English language
  • Intermediate skills in Microsoft Office Suite
  • Experience in the pharmaceutical industry or CRO environment (highly desirable)

To apply

  • To apply for this role please click on the 'apply for this job' link and submit your CV along with a cover letter outlining your skills and experience, please submit as one Microsoft Word document.
  • To be considered for this role you must be able to provide evidence of entitlements to work in Australia.
  • As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process.
  • For further information about CPR Pharma Services, please visit our website at http://www.cprservices.com.au

CPR Pharma Services is an equal opportunity employer

 

 

 

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