Cardiff, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include 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 »
/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 »
support to internal teams and external partners. Requirements Bachelor's degree in a relevant scientific discipline. Experience in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with 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 »
service cardiovascular contract research organisation (CRO) powered by an integrated Clinical Research Platform and a Global Site Network. We provide research solutions to our Pharma, Biotech and CRO partners via: CYTE Connect, our integrated clinical platform that allows seamless collaboration for sites, sponsors and CROs; CYTE Locate, our global site more »
Newport, Shropshire, West Midlands, United Kingdom
Omega Leeds
and efficiency projects within a quality driven manufacturing environment BSc/BEng in Process or Chemical Engineering or related Engineering Experience of Process/Pharmaceutical/FMCG or other regulated industry such as food and drink Operational knowledge of manufacturing equipment Track record of leading engineering projects in manufacturing processing more »
Advise on migration roadmap to SAP S/4 HANA Industry experience of SAP S/4 implementation in manufacturing industries, consumer packaging goods, pharmaceutical, or retailThe Person Functional expertise and knowledge of the latest SAP Digital Supply Chain suite and roadmap Deep understanding and knowledge of digital Supply Chain 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 »
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 »
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 »
providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we helpbiotech and pharma customers save precious time and money in getting drugs to patients. As a growing and successful business, we employ more than 1,300talented individuals globally 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 »
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 »
PhD and/or MBA in the field of Biology, Biochemistry, or related Engineering is preferred.Advanced no of years of commercial experience in the Pharmaceutical, Biotech or CDMO space. Proven track record in delivering year on year financial and customer satisfaction targets. General understanding of drug development and commercialization pathways. more »
