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 »
brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects more »
Company description: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over more »
brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects more »
brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects 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 »
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 »
Slough, Berkshire, South East, United Kingdom Hybrid / WFH Options
Ad Warrior
some of the worlds largest and most successful Brands and Agencies, delivering enterprise scale technology and marketing transformation programs across sectors such as, FMCG, Pharma, Telco, Retail, Travel, Financial Services, Insurance, Manufacturing, Automotive, Utilities, Public Sector, Marketing & Advertising Agencies and Technology Vendors. In the last few years, they have focused 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 »
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 »
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 »
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 »
ability to use MSOffice applications e.g. Word and Excel Demonstrates good general clinical knowledge and skills Demonstrates basic knowledge and understanding of GMP Effective pharmaceutical skills Understanding of clinical risk and clinical governance Identifies own training needs and maintains a portfolio of practice Desirable Knowledge of basic IMP management Knowledge more »
Manchester Area, United Kingdom Hybrid / WFH Options
Factorytalk
continuous improvement. Job Description: Join us in creating and deploying next generation MES solutions using the Tulip (https://tulip.co/) platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the MES concept. So, as well as knowledge and experience of MES and GxP IT projects, you more »
