and supported by the Consultant Pharmacist - Diabetes and Principal Transplant, Renal and Urology Pharmacist Person Specification Professional/Statutory Registration Essential Registration with General Pharmaceutical Council Qualifications/Education Essential MPharm degree (or recognised equivalent) Postgraduate Clinical Diploma in Pharmacy Practice or equivalent training, experience. Non-medical prescribing qualification and more »
Title: Automation Project Manager - Global Pharma Location: Near Watford Company Summary My client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. By joining my client, you will be working for an organisation with a human healthcare philosophy, which means … Desirable - Practical experience working on manufacturing execution systems (MES) OT Cybersecurity knowledge Experience working with edge computing/IIoT Practical experience working within the pharmaceutical industry Experience of serialisation/vision systems and interfaces to enterprise systems Practical experience working with Siemens PLCs and HMI software Experience of working with … pharma.co.uk If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/ more »
SENIOR DATA SCIENTIST (FTC) HYBRID (London) £60,000 - £70,000 COMPANY: We are working with a consultancy, specialised in healthcare/pharma analytics. They are looking to bring in a Senior Data Scientist on an FTC to work with one of their biggest clients. ROLE: Work directly with a team more »
Stevenage, Hertfordshire, South East, United Kingdom
CMR & Life Sciences
Project Controls Manager Pharmaceutical, Automation Stevenage, Luton, St Albans, Harlow Permanent Position £65000 to £75000 Position Overview: We are seeking a highly skilled and experienced Project Controls Manager to join our dynamic team. The successful candidate will be responsible for the planning, scheduling, cost management, and overall project controls for more »
/create new SOPs Where change controls require participation in the packaging part, raise packaging specifications and check Master Batch Packaging records from Central Pharma Support Team with the process of movement of goods for products and materials through SAP system, including, purchasing, receiving, moving from site to site etc. more »
to influence peers and exec-level staff. Good knowledge of IBM Maximo is required along with hands on experience working in industries such as Pharmaceutical, Oil and Gas, Facilities Management, manufacturing or Travel and Transport. PLEASE NOTE that sponsorship is not available for overseas candidates. more »
documented accurately. Ensure all equipment is suitable for use. The ideal candidate will have the following: A relevant BSc degree, eg Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent. Be computer literate, with good working knowledge of MS Office. Experienced in QC testing of API, including HPLC and GC. Other more »
CMOs) Develop knowledge and create IP opportunities for the portfolio Requirements Minimum 8 to 10 years’ experience as a drug project manager in a pharmaceutical and/or biotech company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late more »
Role Provide technical engineering support to the Macclesfield Campus Teams Assisting in the management of Engineering, Safety Health & Environment, and Goods manufacturing compliance Supporting pharmaceutical operations such as HVAC, Purified Water systems, automated control systems Assisting with Site Asset Management Strategy and delivery of Asset Life Cycle activities Propose and more »
in SuiteScript (JavaScript) programming language for custom script development and automation. Experience of large-scale organisational change and ERP technology transformation Experience in PV pharma or Life Sciences industry-specific processes and best practices. Awareness of operating frameworks such as, CCMP, ITIL V4, GDPR, ISO27000, ISO27001. Cyber Essentials, ISO9001, GAMP5 more »
Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We more »
ourselves on being a leading provider of comprehensive engineering project delivery services across a wide range of industries, including food and drink, homecare, chemical, pharmaceutical, warehousing and even construction! From installing packaging lines to providing hygienic processing solutions you name it, we've already done it or we are currently more »
degree or equivalent qualification in Sciences or Life Sciences subject Experience within the medical device industry or a similarly heavily regulated industry such as pharma or nuclear Experience of, and a good basic knowledge of engineering documentation and drawings Experience of both quality management systems and complete engineering lifecycles and more »
the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with more »
technical files, and post-market surveillance. A minimum of 8 years post-qualification experience in regulatory affairs in the medical device and/or pharmaceutical industry in product registration, medical device file, and/or technical compliance activities. Due to the organisation's rapid growth, there is extensive opportunity to more »
leader in water recovery, treatment, and reuse. We design, supply, and service a range of water systems and monitoring equipment in industries ranging from pharmaceutical to food and beverage applications, and from microelectronics ultrapure water to municipal water and industrial wastewater treatment. We are one of the world’s leading more »
enable our clients to meet the changing needs of the global landscape. Required Understanding of Supply chain planning domain, preferably in Life Science or Pharma Industry Have multiple cycles of leading implementation experience in complex supply-chain solution design, development, and testing. With at least, 1 full cycle Kinaxis implementation more »
Essex, England, United Kingdom Hybrid / WFH Options
Walker Hamill
listed organisations, private equity backed businesses and privately owned companies. We recruit across all sectors and have particularly strong client relationships in media, retail, pharma/biotech, technology, property/real estate, leisure and business services. Headquartered in London, we have additional offices in continental Europe. For more information, please more »
Kestrel Court, Waterwells Drive, Waterwells Business Park, Quedgeley, Gloucester, England
FAIRFIELD CONTROL SYSTEMS LIMITED
critical infrastructure where you could be involved in: Flood defence schemes Aerospace facilities Moving bridges and structures Manufacturing facilities Roller coasters and leisure rides Pharmaceutical facilities Training The Level 6 Apprenticeship degree programme is provided by the University of Warwick. The BEng Electromechanical Engineering Degree Apprenticeship is a full Warwick more »
West London, London, United Kingdom Hybrid / WFH Options
People First Recruitment
skills Budget management Market intelligence building, benchmarking and analysis Experience in the assessment of identified CMOs through procurement sourcing processes Ideally experience in the pharmaceutical sector Experience in managing relationships with CMOs Experience in developing sourcing strategies and managing their implementation across multiple geographies and supply chains Experience in managing more »
vast experience in M&A, IT and transformation services in the Life Science industry. Our current client base is predominantly in the Medtech and Pharma industry. Our team transforms complexity into priority actions, a clear timeline, and executive decisions supported by appropriate governance. You will be able to work with more »
unsupervised. Good knowledge of the principals and guidelines for GDP as set out in the Green Guide Experience of working a medical device or pharmaceutical quality function Qualified Internal Auditor Desirable: Good knowledge of the requirements of the MDD/MDR as well as ISO13485 & ISO9001 Ability to work in more »
Oxford, Oxfordshire, South East, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
or maintaining advanced or capital equipment in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc. more »
