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Base pay range
Direct message the job poster from Cpl Life Sciences
Principal Consultant – Quality/Scientific
I am working with a pharmaceutical manufacturing company based out of Camberley, England who are looking for a Quality Assurance consultant to join on an initial 6 month contract.
Job Purpose:
* To ensure compliant and efficient execution of a quality project across the UK and Ireland organizations.
* Gap assessment of the QMS for a new entity.
* Project planning to ensure effective and compliant integration of current QMS with to be QMS of the established entity.
* Ownership of the project planning and execution.
* Implementation of project plan to ensure effective QMS in new entity.
* Creation of Quality agreements and contracts.
Experience:
* 1-3 years experience in the pharmaceutical industry, GxP knowledge.
* Good level of skills in the use of computer based systems and applications.
Functional Quality Knowledge/Skills:
* Quality System Management.
* Understand Regulatory Environment - Knowledge of GMDP and other regulatory requirements relevant for country organisation.
* Quality Governance/Compliance - Support preparation for audits and inspections.
* Project management experience for Quality.
If you are interested please apply or send me a message at jamie.keith@cpl.com.
Seniority level
Associate
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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