With over 60 years of global experience, Wickham Micro Limited are a world leader in providing contract microbiology services to the pharmaceutical and medical device industry; ensuring the products we test are safe and effective for their intended use. Our Company is a great place to work, and we want you to enjoy working with us. There are various ways in which you can progress, whether you wish to become a Subject Matter Expert in a particular area or climb the ladder and become a more senior member of the team – you tell us, and we will work with you to help you achieve your goals About the Role: An exciting opportunity has arisen at our Head Office in Gosport for a Biocompatibility Moderator within our Biocompatibility department on a FULL-TIME basis, working 8am – 4pm Monday - Friday with occasional overtime and weekend work. The purpose of this role is to oversee the subcontracting of biocompatibility GLP studies when WML is acting as the sponsor. Main Duties to: Act as a Study Director to assure that the scientific, administrative and regulatory aspects of each GLP study are controlled. Have responsibility for Study Plan design and approval. Drawing final conclusions to the GLP study. Collating data for each GLP study. Handling Multisite studies Selecting the appropriate approved subcontractor. Oversee sample management between the client, WML and subcontracting testing laboratory. Oversee quotes from subcontractors and handling purchase orders. Compiling and reviewing test item characterisation provided from the client. Completing Test Item Datasheets (TIDS). Reviewing GLP study Plans (device information and extraction methods) and liaising with the client on approval. Reviewing GLP study reports (results) and liaising with the client on approval. Dealing with all queries related to active Biocompatibility projects. Additional Duties to: Assisting sales with biocompatibility quotes, questions, and queries. Providing clients with alternative options and support in root cause analysis in the instance of any adverse outcomes. Provide internal training on the principles of GLP. Regular review of relevant pharmacopoeias and standards, conducting gap analysis. Qualifications/Role Requirements: A minimum of 5GCSE’s or equivalent, including Maths, English and Science. Degree (or equivalent) in a life sciences subject. Knowledge of the MS Office suite and Outlook, in particular Excel is essential. In depth knowledge in GLP, ISO 17025, 10993 & 18562. Possess a high degree of personal integrity with strong problem-solving skills and high attention to detail. Excellent organisational and interpersonal skills and ability to train effectively to all levels of the organisation. Ability to challenge and drive quality and a compliant culture forward and deliver against milestones. Proven ability to multitask and work unsupervised. Salary: Starting salary £24,000 depending on experience Our benefits package seeks to reward you for your dedication and commitment. Here’s what we can offer you: Occupational sick pay scheme. An additional day off for your birthday (upon successful completion of your probationary period). Auto-enrolment into our Pension scheme. Cycle to Work scheme. Health and wellbeing support through our Employee Assistance Programme and Mental Health First Aiders. Plenty of free on-site parking. Free tea, coffee, hot chocolate and fresh fruit. Option to be part of our Medical Cashback Scheme (upon successful completion of your probationary period), allowing you to claim back on things such as dentist fees, opticians, physiotherapy, counselling and much more. Life assurance. Company events The opportunity to be part of an experienced team that is constantly evolving with the Company. If you are shortlisted for an interview, this will be held virtually in the first instance to ensure the role is the right fit for you. Following that, you may then be invited on-site for a second interview with the managers of Quality Assurance. This will help you to gain a greater understanding of the role itself and the work we carry out here at Wickham Micro. Applications will only be accepted from individuals who are eligible to live and work within the UK Wickham Micro Limited is an equal opportunities employer. We are committed to fostering an inclusive work environment where all employees and applicants are treated with respect and dignity. We encourage individuals from all backgrounds, including but not limited to race, gender, age, disability, sexual orientation, religion, or any other characteristic, to apply.