QA Consultant
other jobs Exact Sourcing Ltd
Added before 5 Days
- England,East of England,Cambridgeshire
- Full Time, Permanent
- £60,000 - £80,000 per annum
Job Description:
The Role of QA ConsultantWe are seeking an experienced Principal QA Consultant to provide GCP Quality Assurance consultancy support to clients involved in clinical drug development. This is a senior, client-facing role with responsibility for delivering high-quality QA services, managing quality systems, and supporting clinical development programmes in a regulated environment.
Key Responsibilities of QA ConsultantTechnical & Consultancy Responsibilities
*Act as a GCP QA Consultant to clients, providing QA support across clinical development programmes
*Manage Quality Management Systems (QMS) for clients
*Prepare, implement, and maintain core Standard Operating Procedures (SOPs)
*Deliver GCP training seminars to client teams
*Perform Quality Control (QC) reviews of essential clinical trial documentation
General & Business Responsibilities of QA Consultant
*Support business development activities, including preparation of proposals
*Prepare invoices and oversee budgets for assigned projects
*Maintain the organisation’s reputation as an ethical and expert consultancy
*Ensure strict confidentiality of clinical trial participants, client information, and company data
*Build and maintain strong professional relationships with clients, investigators, suppliers, and consultants
*Work collaboratively with colleagues to promote a positive team culture
*Contribute ideas to support efficient company operations and continuous improvement
*Maintain awareness of ongoing projects and overall business activities
*Effectively plan and manage personal workload
*Maintain technical expertise through continuous professional development
*Work in accordance with internal Standard Operating Procedures
Qualifications & Experience of QA Consultant*BSc (or equivalent) in a life science discipline
*Relevant experience in clinical drug development
*Strong understanding of the regulatory environment for conducting clinical trials
*Demonstrated experience in GCP Quality Assurance
*Competent IT and word-processing skills, including Microsoft Office applications
If you feel that the QA Consultant role is for you then please do apply.
By applying for this QA Consultant you are agreeing to your CV being held on our database, stored confidentially and securely. Your CV details will be used and kept only to provide recruitment services from us. We will only send your details to clients once discussed with you and your data will not be shared with any other third party. You can ask for the deletion or correction of your data, or to opt out of this service at any point by informing Exact Sourcing.
We very much look forward to hearing from you and will be reviewing all applications over the next 2 to 3 weeks. If you are selected, we will be in contact and if not, we will be keeping your details on file for any future vacancies.
Exact Sourcing is an equal opportunities employer.
Key Responsibilities of QA ConsultantTechnical & Consultancy Responsibilities
*Act as a GCP QA Consultant to clients, providing QA support across clinical development programmes
*Manage Quality Management Systems (QMS) for clients
*Prepare, implement, and maintain core Standard Operating Procedures (SOPs)
*Deliver GCP training seminars to client teams
*Perform Quality Control (QC) reviews of essential clinical trial documentation
General & Business Responsibilities of QA Consultant
*Support business development activities, including preparation of proposals
*Prepare invoices and oversee budgets for assigned projects
*Maintain the organisation’s reputation as an ethical and expert consultancy
*Ensure strict confidentiality of clinical trial participants, client information, and company data
*Build and maintain strong professional relationships with clients, investigators, suppliers, and consultants
*Work collaboratively with colleagues to promote a positive team culture
*Contribute ideas to support efficient company operations and continuous improvement
*Maintain awareness of ongoing projects and overall business activities
*Effectively plan and manage personal workload
*Maintain technical expertise through continuous professional development
*Work in accordance with internal Standard Operating Procedures
Qualifications & Experience of QA Consultant*BSc (or equivalent) in a life science discipline
*Relevant experience in clinical drug development
*Strong understanding of the regulatory environment for conducting clinical trials
*Demonstrated experience in GCP Quality Assurance
*Competent IT and word-processing skills, including Microsoft Office applications
If you feel that the QA Consultant role is for you then please do apply.
By applying for this QA Consultant you are agreeing to your CV being held on our database, stored confidentially and securely. Your CV details will be used and kept only to provide recruitment services from us. We will only send your details to clients once discussed with you and your data will not be shared with any other third party. You can ask for the deletion or correction of your data, or to opt out of this service at any point by informing Exact Sourcing.
We very much look forward to hearing from you and will be reviewing all applications over the next 2 to 3 weeks. If you are selected, we will be in contact and if not, we will be keeping your details on file for any future vacancies.
Exact Sourcing is an equal opportunities employer.
Job number 3351270
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Company Details:
Exact Sourcing Ltd
Company size: 1–4 employees
Industry: Sales
CORE VALUESOur personal recruitment service and honesty underpins our process. We are committed to meeting all our candidates in person before shortli...