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| Job Location | Harlow |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
CK Group are recruiting for a Qualified Person to join a company in the healthcare industry at their site based in Harlow on a on a contract basis for 11 months.Salary:Competitive hourly rateQualified Person Role:· Undertake QP responsibilities for certification and release of intermediate and finished IMP in compliance with GMP, Manufacturing Authorisation, Clinical Trial Application and regulatory requirements.· Interpretation and communication of GMP regulatory requirements to staff and customers including Investigational Medicinal product specific GMPs and their interface with GCPs.· Review and approval of non-conformance including deviations, customer complaints, out of specification investigations.· Review and approval of control documents e.g. SOPs, quality agreements, Packaging records.Your Background:· Must be eligible to act as a QP for Investigational Medicinal Products, as defined by The Medicines for Human Use (Clinical Trials) Regulations 2004 under permanent provisions.· Experience working with oral solid dosage forms, including capsules and tablet formulations and /or inhalation products including non-sterile liquids and suspensions. · Strong decision-making skills based on GMP requirements.· Experience of sterile products would be an advantageCompany:Our client is a global healthcare company, taking on some of the worlds biggest healthcare challenges.Location: This Qualified Person role will be based at our clients site in Harlow, Greater London. Apply:For more information, please contact Natasha Young on or email . Please quote reference 49760.Please note that the successful applicant will be required to engage via an FCSA-accredited and CK-approved umbrella company and the rate of pay indicated is an umbrella rate.