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 »
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 »
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 »
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 »
Hillingdon, 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 »
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 »
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 »
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 »
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 »
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 »
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 »
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 »
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 »
Medpace Overview Medpace 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 »
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 »
Company description: 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 »
and supported by the Consultant Pharmacist - Diabetes and Principal Transplant, Renal and Urology Pharmacist Person Specification Professional/Statutory Registration Essential Registration with General Pharmaceutical Council Qualifications/Education Essential MPharm degree (or recognised equivalent) Postgraduate Clinical Diploma in Pharmacy Practice or equivalent training, experience. Non-medical prescribing qualification and 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 »
SENIOR DATA SCIENTIST (FTC) HYBRID (London) £60,000 - £70,000 COMPANY: We are working with a consultancy, specialised in healthcare/pharma analytics. They are looking to bring in a Senior Data Scientist on an FTC to work with one of their biggest clients. ROLE: Work directly with a team more »
Stevenage, Hertfordshire, South East, United Kingdom
CMR & Life Sciences
Project Controls Manager Pharmaceutical, Automation Stevenage, Luton, St Albans, Harlow Permanent Position £65000 to £75000 Position Overview: We are seeking a highly skilled and experienced Project Controls Manager to join our dynamic team. The successful candidate will be responsible for the planning, scheduling, cost management, and overall project controls for more »
