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 »
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 »
Stafford, Staffordshire, United Kingdom Hybrid / WFH Options
Confidential
computer software such as MS Word, MS PowerPoint, MS Project, and VisioEducation/Experience: PMI or PMP certification preferred Experience in project management,in pharmaceutical or related industries Experience with Software as a Service (SaaS) platformsAdditional Requirements: Collaborative mindset Open, honest, and transparent communication style Leadership qualities Client and stakeholder 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 »
or an MBA. 5+ Years' experience in Strategy, Management Consulting or Industry; with a dedicated focus and background on Healthcare and Life Sciences; (i.e., Pharma, Biopharma, Biotech and Medical Device). Proficiency with Microsoft Office, including Word, Excel, and PowerPoint; (experience in computer programming software (e.g., VBA) or other role more »
wider business. Flexibility to work across multiple sites in London Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. 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 »
Stevenage, England, United Kingdom Hybrid / WFH Options
Workday
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 »
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 »
support for the company’s initiatives. Requirements: Bachelor's degree in a relevant field (think: Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products 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 »
leads and inspires colleagues. • Strong influencing and leadership skills. Understands influencing, stakeholder management and negotiation strategies. The Client is ideally seeking someone from a Pharmaceutical or Bio Science background and who understands how to work with the government and government funding. This position will manage 15 people within the IT more »
programme | Recognition awards | Free Parking Bespak Holmes Chapel is an Investors in People silver award winner who employs over 300 people and are a pharmaceutical Contract Development and Manufacturing Organization (CDMO) that offers development and manufacturing solutions for a variety of medical products. Our products include medical devices such as more »
Experience with MS Azure stack and/or Databricks Experience with Docker Knowledge and experience of people data landscape . Experience in healthcare or pharmaceutical industries. 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 »
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 »
challenges, with experience in quality management systems and tech transfer. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. more »
Oxfordshire, South East, United Kingdom Hybrid / WFH Options
Hays
scientific or laboratory setting.Other key deliverables include: A proven track record of successfully designing and implementing a QMS within a Life Science Research environment, pharma or biotech. The ability to be adaptable to new challenges and changes within a company bringing a flexible approach to day-to-day operations. Strong 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 »
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 »
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 »
