Julie Marshall is recruiting for a Quality Assurance Coordinator to join a company in the Pharmaceutical industry at their site based in Essex on a contract basis for 12 months.
The main purpose of the role will be to:
Ensure quality and compliance of Investigational Medicinal Products used worldwide in conjunction with business partners.
Review validation documentation for compliance to cGMP, SOPs, internal and regulatory requirements.
Highlight quality and compliance issues and provide assistance to business areas on quality matters.
Assessment of deviations and impact assessments, make recommendations for corrective and preventative actions.
Support continuous improvement as directed.
In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
BSc degree (or equivalent) in a Scientific or Quality discipline.
Knowledge of clinical trials and investigational medicinal product supply.
Experience working in a pharmaceutical environment with knowledge of cGMP and Quality Assurance would be beneficial.
Experience in change management.
Experience in providing QA oversight to significant projects.
Proficient with Office applications (e.g. Word, Excel).
Experience of working in a team environment.
This is an excellent opportunity to join a global company based in the Essex region.
CK Group is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST39539 in all correspondence.
You must be eligible to work in the UK. Learn more
- Agency: CK Group (Science, Clinical, Engineers and IT Recruitment)
- Posted: 10th July 2017
- Expires: 7th August 2017
- Reference: ST39539