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 »
or related field(s). Excellent SAS programming skills (BASE, MACRO, GRAPH). Excellent knowledge of CDISC standards. Statistical Programming experience within a CRO Pharmaceutical/Healthcare/Biotechnology industries. Experience in statistical programming initiatives, and development of processes. Knowledge and experience in database design and structures. The ability to 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 »
TGA and FDA regulations desirable Minimum of 7 years’ experience working as a GCP Quality professional in a management/leadership role within a Pharmaceutical/Biotechnology industry Experience at conducting service provider, site and internal audits highly desirable Experience of building and maintenance of Sponsor Oversight File (SOF) Experience 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 »
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 »
detail. Medpace OverviewMedpace 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 »
Chain process area SAP system design, build and deployment experience – 4 full lifecycle implementations preferred Experience of SAP in Manufacturing industries, Consumer Packaging Goods, Pharmaceutical, Oil and Gas, or Retail Experience of facilitating a design workshop and then translating the requirements into design Experience of managing small teams, coaching and 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 »
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 »
ExperienceMust have strong experience of working in Information Technology, especially the delivery and support of on-premise and cloud-based IT applications.Must have a Pharmaceutical backgroundMust have experience of Service Delivery and Service NowStrong skills in managing a diverse team of global staffExcellent interpersonal and communication skills with the ability more »
The Senior Pharmacy Technician for Pharmacy Purchasing and IT systems is responsible for: Ensuring compliance with standing financial instructions and national standards for NHS pharmaceutical procurement services Organising the pharmacy procurement and homecare team The maintenance and development of IT systems in the pharmacy department In managing the pharmacy stock 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 »
other quality systems. Must understand GXP. Order of focus - GCP, GDP/GMP and then GLP. Extensive experience and knowledge in Quality Assurance in Pharma/biotech space to interact with stakeholders. Not a validation specialist but understands the sequence and what that process needs and is involved. Data tools more »
Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects in the pharmaceutical and/or biopharmaceutical sectors. Working with other departments and key stakeholders Good communication skills and be proactive Successful candidates will be able to demonstrate more »
Organic Laboratory Department Head | Cambridgeshire | £40,000 - £60,000 Our client is a leading provider of analytical services to customers across multiple industries including pharmaceutical, food, environmental and cosmetic. With laboratories spanning across the globe, an exciting role has arisen in Cambridgeshire to contribute towards the success of their Environmental more »
Uxbridge, England, United Kingdom Hybrid / WFH Options
ISR Recruitment
that provide the technology to enable the launch of new therapies and drugs Must have commercial experience delivering into and for life sciences/pharmaceutical/biotechnology sectors Platforms in scope include: Salesforce.com, Oracle EBS, AWS, Tableau and Sitecore Proven experience working with dispersed and global teams across multiple locations more »
