We’ve an exciting opportunity for a hard-working individual who is capable of working independently and as team. To ensure cover across all GMP Sites travel to Manchester site would be required Main Responsibilities Inspection and approval of clinical trial medicinal products Review of associated documentation Ability to prioritise workload and deal with changes to priorities to support a fast-paced ever changing manufacturing environment Liaise and communicate with multiple departments to facilitate the on-time release of products. MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations. Good interpersonal skills Very good skills with Microsoft Office (eg Word, Excel) The ability to write clear and concise reports Good attention to detail and excellent organisational ability Sufficient initiative to be able to work alone and with a team GMP Production experience would be an advantage Background in Microbiology, Chemistry or similar life science would be an advantage Some experience in a clinical environment would be useful Competitive salary in keeping with pharmaceutical industry standards that will reflect experience Health Insurance Eye Care Vouchers Cycle to work scheme Free onsite parking 25 days annual leave (increasing in increments to 30 days after 6 years' service) Your birthday off work Please email [email protected] should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.