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| Job Location | Tredegar |
| Education | Not Mentioned |
| Salary | £20,000 - £25,000 per annum |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Science Solutions - Development Analyst - South Wales Suitable backgrounds includeMCHEM / BSC Grads with a desire to move up in Method DevelopmentQC Backgrounds with some experience from research in method development/column changes using HPLC or related Development Analytical experience from a relevant chemistry Lab Including APIs, Medicinal, Small MoleculeSalary:c£20-£28kWe are currently looking to recruit an junior & experienced Development Analysts for an established pharmaceutical manufacturer with an excellent team and culture. The role is to support the companys development and testing activities on a project related to the introduction of a new pharmaceutical product.Qualifications / Previous Experience / General Attributes (Person Specification):All analysts should:* Hold a degree in Chemistry or pharmaceutical science or closely related discipline. * Be self-motivated * Methodical, organised and have an excellent attention to detail. * Able to work both in a team & independently * Good communication skills are essential as role requires the organisation and co-ordination of work with other departments.* At least three years experience in carrying out HPLC analysis in a Pharmaceutical or ISO17025 accredited laboratory including analytical method development.Roles & Responsibilities:· Development and validation of analytical test methods in an efficient and effective manner in full compliance with ICH Q2, relevant documented procedures and pertinent regulatory/company requirements. · To plan and prioritise own day to day workload in line with client requirements and adapt this where necessary in line with client needs and expectations. · To assist in preparation of technical documentation within the Department, as required. · To assist in training of others, as required. · To ensure that all work carried out complies with departmental procedures and is cGMP compliant. · To review analytical and laboratory data within the team for accuracy, completeness and compliance with documented procedures. · To communicate effectively with others on site and to assist with departmental problem solving as required.If you are successful at first interview then a second practical interview including aptitude tests will be part of the recruitment process.Please apply now to be considered immediately Required skills
Keyskills :
GMP HPLC ICP QC Pharmaceuticals