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 »
regulatory requirements and market dynamics is not necessary but a strong advantage •Proven experience within a CDMO or a similar commercial role within biotechnology, pharmaceutical and life-science consulting industry is advantageous •Excellent written and verbal communication skills, with the ability to present findings and recommendations in a clear and 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 »
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 »
to handle any commercial, industrial, or one-of-a-kind challenge. We are a trusted contractor to diverse industries, such as aerospace, biotech/pharmaceutical, education, healthcare, entertainment, hospitality, manufacturing, and retail, to name a few. Our services also include energy solutions and have earned a reputation as a premier 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 »
working with minimum supervision under pressure to tight deadlines with customer focus. Requirements : Bachelors degree in applicable field (e.g Science, Engineering) or equivalent (e.g Pharma, Biopharm, Life Science, Biotech) Good Experience in Quality Assurance; Problem Solving, Analytical and Continual Improvements. Certified Lead Auditor in ISO 9001:2015 or more »
ensuring equipment performance? We are seeking a highly motivated Equipment Validation Specialist to play a vital role in maintaining the integrity and efficiency of pharma manufacturing processes. In this role, you will be responsible for: Defining and executing equipment validation activities , ensuring all equipment meets the required standards. Coordinating and 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 »
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 »
software, data analytics tools, process mapping software). Ability to leverage technology solutions to streamline processes, enhance efficiency, and drive innovation. Experience in PV pharma or Life Sciences industry-specific processes and best practices. Awareness of Operating of operating frameworks such as, CCMP, Lean Six Sigma, ITIL V4, GDPR, ISO27000 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 »
of their work Requirements: Education & Experience: PhD in Immunology, Cell Biology, Biomedical Sciences or related field 2 years' productive experience in the biotechnology or pharmaceutical industry in biologics drug discovery; minimum of 2-4 years' productive postdoctoral experience in an industry or academic laboratory Demonstrated success in contributing to biologics 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 »
have any questions, please contact Ingrid Aymes at i.aymes@proclinical.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 »
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 »
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 »
/data analysis, business intelligence or related field. Fluent in English both written and spoken, any other languages are an asset. Experience in the pharma industry and/or beauty & personal care industry is a plus together with knowledge of classic Forecasting methodology and predictive analysis. Excellent communication skills with more »
