as LIMS, ELN, SDMS, CDS, or similar systems. Expert level understanding of laboratory processes, data management principles, and laboratory workflows in various domains (e.g., pharmaceutical, biotechnology, manufacturing). Knowledge of regulatory requirements and compliance standards relevant to laboratory operations (e.g., FDA 21 CFR Part 11, ISO 17025, GLP, GMP). more »
for adhering to all health and safety guidance, provided by the Company. EXPERIENCE WE ARE LOOKING FOR:- Experience from a directly relevant biotechnology or pharmaceutical industry Experience of working in a busy laboratory environment D or MD/Ph.D in relevant scientific discipline, Master’s degree or native equivalent with more »
offer: Bachelor sdegree in Statistics, Mathematics, Computer Science or related discipline, advanced degree preferred 10+ years (5+ years for advanced degree) experience in a pharmaceutical industry, CRO or another clinical research setting Excellent knowledge of statistical programming including SAS/Base, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA more »
Great Ormond Street Hospital for Children NHS Foundation Trust
close them, to review the quality risk and implication to the batch with the QP as well as ensuring these are reflected in the Pharmaceutical Quality Management System. The QA Technical Lead will assist and support the QP in duties delegated to them by the QP and confirm compliance with more »
as needed. Qualifications: Bachelor's degree in a relevant scientific discipline; advanced degree preferred. Minimum of 5 years of experience in Quality Assurance for pharmaceutical or biotechnology products. Extensive experience in GCP auditing, including internal, external, and Investigator Site audits. Strong knowledge of regulatory requirements and guidelines related to GCP more »
Bachelor´s degree in Statistics, Mathematics, Computer Science or related discipline, advanced degree preferred 10+ years (5+ years for advanced degree) experience in a pharmaceutical industry, CRO or another clinical research setting Excellent knowledge of statistical programming including SAS/Base, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA more »
Risk Management 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 »
Uxbridge, West London, United Kingdom Hybrid / WFH Options
Confidential
management skills, cross-functional engagement and organizational skills To be considered, you must have a Bachelor's degree and minimum of 12 years relevant pharmaceutical industry experience, 8 years within Clinical Trial Management. Experience with early phase clinical trials is highly preferred. Does this sound like you? Apply now to more »
Chronicle Lead 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 »
Prime, Golden Ventures, and Google's AI fund, Gradient Ventures, we provide an indispensable tool for scientists that accelerates research at 16 top 20 pharmaceutical companies and over 4,300 leading academic centers. We're a certified Great Place to Work, and top-ranked company on Glassdoor. Our Culture: BenchSci more »
Proactive. Projects a positive and professional image at all times. Experience Essential Extensive demonstrable experience of research governance management in the NHS, academia, or pharmaceutical industry, working to ICH GCPs. Demonstrable experience of IRAS submission system. Demonstrable experience of creating and working to Standard Operating Procedures. Significant experience of leading more »
media and telcosConsumer Business; ranging from automotives to consumer goods and retail companies as well as travel, hospitality and services;Life Sciences; from global pharmaceutical organisations to MedTech startups, where we help organisations transform their operations to succeed against a radically changing backdrop of the future of health, andEnergy, Resources more »
to sustainable science with the goal to make the world healthier, greener and cleaner. Our customers span a broad range of market segments including pharmaceutical, biotech, contract research and contract manufacturers as well as clinical, forensic and academic laboratories in addition to organizations focused on food safety, clean water and more »
Director of CMC (Biologicals) taylorollinson Director of CMC (Biologicals) Industry Sector Biotechnology , Chemical , Medical Devices , Pharmaceutical , Other Profession Laboratory Operations & Research , QA & Regulatory Location UK , East Anglia Salary Competitive Base + bonus + share options Description Director of CMC Location: Cambridge Contract: Full-time and permanent (Monday to Friday) (Part more »
and problem solving skills Ability to collaborate effectively across global teams and communicate complex ideas in a simple manner Preferred Qualifications Financial Services or Pharmaceutical industry experience Experience in distributed system design Experience with Pure/Alloy Working knowledge of open-source tools such as AWS lambda, Prometheus Spark, Hadoop more »
Weybridge, England, United Kingdom Hybrid / WFH Options
Clinigen
Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world. We are currently 1,100 people more »
problems, as well as purchase clinical-grade, personalised skincare. We have dedicated in-house clinical teams authorised to prescribe medications, and we own a pharma business capable of manufacturing many of the medicines and skincare products we provide. We re an in-house, Direct-To-Consumer (D2C) proposition all the more »
Quality Assurance Specialist – Relocation to Ireland Our client is a global company with a site in Ireland and provides solutions for animal health and nutrition. The product line helps prevent, control, and treat diseases, improve animal health and performance, and more »
you have any questions, please contact Ingrid Aymes at i.aymesproclinical.com 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 »
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 »
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 »
the Supply Chain process areaSAP system design, build and deployment experience – 4 full lifecycle implementations preferredExperience 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 designAbility to build strong client relationships based on 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 »
