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 »
Job Description Senior Information Security Analyst Our Client is a leading global company specialising in pharma products. They are looking to recruit a Senior Information Security Analyst with at least 5 to 7 years expertise in Technology Security. The Senior Information Security Analyst is responsible for maintaining information security policies more »
Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. more »
various relevant Microsoft platforms, tools, technologies, patterns, and techniques related to Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. more »
About the Position : Location: Liverpool, England ( Onsite ) Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe more »
Ariba and S/4HANA implementations. Experience Record to Report, I2P, RPM/PPM, SOA Manager, ABAP and WebMethods is a plus. Experience in Pharmaceutical Industry, is a plus. Demonstrated technical leadership experience. Understanding of Procurement business processes and Supplier master data. Knowledge of integration of S/4HANA Procurement more »
Saffron Walden, Essex, South East, United Kingdom Hybrid / WFH Options
EMBL-EBI
between the European Bioinformatics Institute (EMBL-EBI), a global leader in the management, integration and analysis of public domain life science data; world-leading pharmaceutical companies GSK, Sanofi, Bristol Myers Squibb, Pfizer and Genentech; and the Wellcome Sanger Institute. Generative AI has revolutionised the way we interact with knowledge. To more »
Saffron Walden, Essex, South East, United Kingdom Hybrid / WFH Options
EMBL-EBI
between the European Bioinformatics Institute (EMBL-EBI), a global leader in the management, integration and analysis of public domain life science data; world-leading pharmaceutical companies GSK, Sanofi, Bristol Myers Squibb, Pfizer and Genentech; and the Wellcome Sanger Institute. Generative AI has revolutionised the way we interact with knowledge. To more »
Stevenage, England, United Kingdom Hybrid / WFH Options
Taleo BE
planning, time management and organizational skills. Experience demonstrating knowledge of essential regulatory guidelines world-wide. Awareness of or experience in clinical space in a pharmaceutical or biotech R&D environment or leading academic research center. Strong written/verbal communication skills and the demonstrated ability to work in a matrix more »
and use of clinical data Experience leading projects with multiple stakeholders Experience of the use and management of Information within the NHS, academic or pharmaceutical community Extensive experience with Microsoft Word, Excel, PowerPoint, and Outlook Experience of documenting results for publication Experience of successfully managing a number of equally important more »
role: Masters or PhD education (Life Sciences, Biochemistry, Biotechnology or similar) Previous experience in process development and tech transfers of biologics (ATMPs preferred) Prior pharmaceutical GMP experience Cell Culture | Upstream | Specialist | MSAT | CMC | Cell Therapy | Technical Operations | Scientist| Downstream | Tech Transfer | MS&T | Technical Transfer | Process Development | GMP | good manufacturing more »
Redcar, North Yorkshire, North East, United Kingdom Hybrid / WFH Options
The Recruitment Co
risks the systems present to regulated business processes To provide and or facilitate quality assurance oversight for the automation of business process associated with pharmaceutical manufacture and distribution To project problem identification/resolution/avoidance; typically involving ongoing interaction with management teams within Tech functions, site and local operating more »
GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements Experience working in a Pharmaceutical/Biotech QC function within a sterile manufacturing site. Proven track record of managing a team within a cGMP QC analytical environment. Degree in a more »
RPi)To support the Head of Quality in ensuring the provisions of the licences are observed. Company Overview: Our client is a rapidly growing pharmaceutical wholesaling company involved in the procurement and supply of unlicensed medicines into the NHS and Private Hospital sector in the UK. They aim to deliver more »
Slough, England, United Kingdom Hybrid / WFH Options
Parkside Recruitment
is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of more »
integration of finance with other SAP areas like MM, PP, IM etc. Familiarity with data science concepts and use cases in Finance. Bio-Tech, Pharmaceutical or Life Sciences experience. Osirian Consulting is committed to working with our clients to promote equality and diversity in the workplace. We encourage and welcome more »
clearly demonstrated. Industry/domain skills: Extensive expertise in finance, HR, sales, marketing, product lifecycle management, manufacturing and post-sales service. Medical device or pharmaceutical industry experience is preferred. Experience in and understanding of a wide variety of analytical processes (governance, measurement, etc.). Experience with agile software development. A more »
A working knowledge of UK regulations is preferred. The candidate will be a convincing communicator with strong interpersonal skills. Previous experience working within the pharmaceutical sector will be advantageous. more »
moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join more »
maintaining the GMP facilities and equipment in accordance with maintenance and validation programmes. The successful applicant will operate within and contribute to a GMP Pharmaceutical Quality System including change control, preventive actions, deviation management and document control. Excellent interpersonal and communication skills are essential, as is the ability to work more »
UK, please find the below job description: 8+ years of strong and hands-on experience in Data Management and Migration, Data Governance Expertise in Pharma domain, its source systems like SAP ERP, SAP BW, SAP HANA, Marketo, Salesforce etc. Proven expertise in gathering requirements from business users and converting it more »
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 »
preventive actions as necessary. Qualifications: Bachelor's degree in a scientific discipline; advanced degree preferred. Extensive experience (10+ years) in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry, with a focus on the UK and Irish markets. Oncology experience is beneficial. Demonstrated expertise in UK and Irish regulatory more »
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 15,000 staff more »
