level in science or equivalent experience. Minimum 5- 7 years of experience in the Regulatory Affairs regulatory experience with new product introduction within the pharmaceutical industry covering both UK National and European regulations Strong communication and project management skills Proficiency in the use of MS Office suite (Excel, PowerPoint) Ability more »
our in-house training. Within the Analytical Sciences department in Sandwich, Kent we specialise in Material Sciences. We support our clients, primarily from the Pharmaceutical Industry, to shape drug product formulations, through defining safe and stable solid forms, investigating drug and excipients attributes, such as physical properties, thermal properties and more »
CK Group are recruiting for a QC Manager on behalf of a growing manufacturer of Active Pharmaceutical Ingredients, to be based at their site in Sandwich on a permanent basis. Joining the company in their state of the art facilities, you will be responsible for managing the QC laboratory and more »
maintenance work, project work and potentially commissioning, for which training can be provided. Work will be carried out in the commercial, retail, hospitality and pharmaceutical sectors. This role would suit an Engineer with experience of BMS works and Trend Systems, looking to develop their skills as a vital part of more »
full solution developments. The AI Lead is comfortable speaking at international regulatory conferences and other events, forming productive networks with labeling professionals inside the pharmaceutical industry as well as technology vendors operating in the labeling or adjacent fields. Through this network the AI Lead identifies emerging technologies of potential interest more »
Dartford, England, United Kingdom Hybrid / WFH Options
Catalent
Business Development Manager Catalent is a global, high growth, public company and leading partner for the pharmaceutical industry in the development and manufacturing of the new treatments for patients worldwide. Your talents, ideas, and passion is essential to our mission: to help people live better, healthier lives Catalent Micron Technologies … Dartford facility specializes in particle size reduction technologies and integrated analytical services for the pharmaceutical industry we are looking for a Business Development Manager to join the team. This role requires the individual to have established API drug substance knowledge and a relentless passion for uncovering new opportunities/business. … industry knowledge of API manufacturing or development, analytical research and scale-up, product manufacturing. Combined sales and/or sales management experience in the pharmaceutical contract services sales (CDMO), pharmaceutical, biotechnology, or life sciences industries. Have a passion, aptitude, & hunter mentality for sales Distinct knowledge of the pharmaceutical industry and more »
Kent, England, United Kingdom Hybrid / WFH Options
SRG
SRG are currently looking for Regulatory Artwork Implementation Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory team on an initial 12 Month basis to be based at their offices in Kent (hybrid). The Role: Responsibility for tracking and real-time transparency of … content of labeling updates and raise issues with the EU ALIM Lead and the Regulatory Strategists. Develop and maintain relationships with relevant stakeholders. Use pharmaceutical packaging and artwork knowledge/experience to collaborate with Manufacturing Artwork Centres. Interact and follow up with all Market Approvers as needed, and re-direct more »
A Coatings Company is currently seeking an Equipment Validation Engineer/Officer to join the team. This pivotal role involves spearheading the creation, development, and support of validation processes, as well as implementing ongoing optimization and harmonization strategies for production more »
line with current government, NICE and BOPA guidelines. Undertaking medicines reconciliation, organising discharge medications, provision of drug information and clinical counselling of patients. Maintaining pharmaceutical care plans for all oncology and haemato-oncology patients. Main duties of the job Supporting and advising our clinicians on safe prescribing within oncology, haemato … line with current government, NICE and BOPA guidelines Undertaking medicines reconciliation, organising discharge medications, provision of drug information and clinical counselling of patients Maintaining pharmaceutical care plans for all oncology and haemato-oncology patients Verification and screening of SACT treatment prescriptions, inpatient prescription charts, discharge and outpatient prescriptions Supporting and … leads within the Nuffield Health group on a regular basis, implementing changes to policy and procedure locally Skills & Experience: UK Registered Pharmacist with General Pharmaceutical Council (Essential) At least 4-5 years of post-qualification experience Experience of supervising and training other staff Post-qualification experience within oncology and haemato more »
