Good Laboratory Practice Quality Assurance Auditor
- Recruiter
- Covance
- Location
- Derby
- Salary
- Competitive
- Posted
- 06 May 2021
- Closes
- 07 May 2021
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
* Are you an auditor looking for a new role in GLP Quality Assurance (QA)?
Do you want to work in the chemical testing * *industry?*
*Do you want to be part of a company that helps build a healthier and safer world?*
As one of the world's premier Contract Research Organisations, we provide research services for a multitude of organisations.We strive to make a difference to people's everyday lives by bringing essential products to the market.
As a *Good Laboratory Practice (GLP)Quality Assurance Auditor* at Covance by Labcorp, based at * Shardlow, Derbyshire * you will play an essential part in making this happen.
*Responsibilities will include:*
* Performing protocol, data, report, and in-lab phase inspections for a specific study type to verify conformance to applicable Standard Operating Procedures (SOP's) and Good Laboratory Practice (GLP) regulatory requirements.
* Evaluating responses to Good Laboratory Practice (GLP) inspection reports and performing follow-up with respondents, management, or others, if needed, to ensure resolution.
* Ensuring that systems used in Good Laboratory Practice (GLP) quality assurance are properly maintained.
* Notifying management of service failures.
* Performing study sign-off including but not limited to quality assurance statement preparation (internal/external) and report finalisation.
* Performing Standard Operating Procedures (SOP's) reviews.
* Participating in internal facility and supplemental inspections, under supervision.
* Deliver basic quality/regulatory training, under supervision.
Identifying opportunities for process improvement and harmonisation efforts that promote best practices.
*What Covance by Labcorp can offer you:*
* Competitive salaries and a comprehensive benefits package including health cover and contributory pension.
* Unrivalled opportunities to develop a successful career in the scientific industry.
* Unsurpassed career development opportunities.
Education/Qualifications:
* A minimum of a Bachelor's Degree in Life Sciences preferred (or equivalent Life Science experience).
* Experience may be substituted for education.
Experience:
* At least 12 months in a regulatory environment.
* Ability to apply basic Good Laboratory Practice regulatory knowledge.
* Ability to follow instruction e.g. QA documents (Standard Operating Procedures - SOP's).
* Ability to assimilate/interpret operational documents such that audit can be performed to required level.
* Ability to critically assess data and apply procedures and regulations.
* Adaptability to an ever changing work environment.
* Ability to recognise gaps in procedures and regulations and consult with more senior QA individuals.
Do you want to work in the chemical testing * *industry?*
*Do you want to be part of a company that helps build a healthier and safer world?*
As one of the world's premier Contract Research Organisations, we provide research services for a multitude of organisations.We strive to make a difference to people's everyday lives by bringing essential products to the market.
As a *Good Laboratory Practice (GLP)Quality Assurance Auditor* at Covance by Labcorp, based at * Shardlow, Derbyshire * you will play an essential part in making this happen.
*Responsibilities will include:*
* Performing protocol, data, report, and in-lab phase inspections for a specific study type to verify conformance to applicable Standard Operating Procedures (SOP's) and Good Laboratory Practice (GLP) regulatory requirements.
* Evaluating responses to Good Laboratory Practice (GLP) inspection reports and performing follow-up with respondents, management, or others, if needed, to ensure resolution.
* Ensuring that systems used in Good Laboratory Practice (GLP) quality assurance are properly maintained.
* Notifying management of service failures.
* Performing study sign-off including but not limited to quality assurance statement preparation (internal/external) and report finalisation.
* Performing Standard Operating Procedures (SOP's) reviews.
* Participating in internal facility and supplemental inspections, under supervision.
* Deliver basic quality/regulatory training, under supervision.
Identifying opportunities for process improvement and harmonisation efforts that promote best practices.
*What Covance by Labcorp can offer you:*
* Competitive salaries and a comprehensive benefits package including health cover and contributory pension.
* Unrivalled opportunities to develop a successful career in the scientific industry.
* Unsurpassed career development opportunities.
Education/Qualifications:
* A minimum of a Bachelor's Degree in Life Sciences preferred (or equivalent Life Science experience).
* Experience may be substituted for education.
Experience:
* At least 12 months in a regulatory environment.
* Ability to apply basic Good Laboratory Practice regulatory knowledge.
* Ability to follow instruction e.g. QA documents (Standard Operating Procedures - SOP's).
* Ability to assimilate/interpret operational documents such that audit can be performed to required level.
* Ability to critically assess data and apply procedures and regulations.
* Adaptability to an ever changing work environment.
* Ability to recognise gaps in procedures and regulations and consult with more senior QA individuals.