- Quality Assurance Representative - North West - £35,000 - £40,000 + Bonus + Benefits (Relocation package if necessary)
A great opportunity has just arisen to join one of the world’s largest and most successful Pharmaceutical companies in a Quality Assurance Representative role working in a cGMP manufacturing environment.
The primary focus of this role is to ensure that products released for sale have been manufactured and packaged in accordance with the licensing requirements, Good Manufacturing Practice and business requirements; and to promote quality/compliance within area of operation.
- Quality Assurance Representative
Do you want to work for one of the largest and most successful Pharmaceutical companies and seeking a challenging and rewarding career?
- Sr GCP Auditor, Clinical Quality Assurance Job
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...
- Clinical Supplies Project Manager
A well-established and International Pharmaceutical resourcing solutions company with multiple capabilities. Including Clinical Supply Services, Global Access Programs (GAP), Pharmacy and wholesale are looking to appoint a Clinical Supplies Project Manager for their site based in South East London. Working in excess of 4,000 packaging requirements with the expectation to grow and develop the business.
- Principal QA Associate- Slough
Chiltern's QA department is looking to recruit a full-time, permanent Principal QA Associate to be based at our Slough Office. This position will support the Operations Group within the Global Quality Assurance Department. Training will be provided however, at least 2-3 years’ previous experience in a similar role is essential. Experience with Databases and eQMS knowledge would be highly beneficial.
- Clinical Research Associate (CRA) - Germany - Phase III Oncology Study - Single-sponsor (Top 5 Pharma)
A home-based CRA position in Germany, working directly for the Sponsor as part of a Global Phase III Oncology Trial.
- Clinical Data Manager
I am working with a firm that specialises with cognitive assessment software and are looking to recruit a Clinical Data Manager position. They will work with their pre-existing ORACLE software and continue to develop their efficiency and needs as a business. This Cambridge based firm have clients that range from Top 30 Pharmas and CROs to public sector institutes and hospitals. The Data Manager will be responsible for carrying out appropriate SOP analysis and coordinate all DM activities.
- Drug Safety Project Manager
I am currently recruiting for a Drug Safety Project Manager for my client based just south of Oxford. As Drug Safety Project Manager, you will be reporting to the director of the pharmacovigilance team, acting as Deputy to EEA QPPV.
- Data Analyst
I am working with a top, Real World Data Firm to recruit a Data Analyst who will create bespoke data solutions for clients who range from Top 30 Pharmas and CROs to public sector hospitals. The data Analyst will assist in creating descriptive primary data monitoring through EXCEL working across phases I, II,III and IV as well as varied therapeutic areas creating a variety of projects to work across at any given point.
- Principal Regulatory Affairs Officer
I am currently recruiting on behalf of our client, a large pharmaceutical company, for an experienced Principal Regulatory Officer. The ideal candidate will have strong experience working with OTC products and keen to develop this knowledge and expertise.