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 »
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 »
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 »
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 »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »
Cardiff, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include 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 »
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 »
/create new SOPs Where change controls require participation in the packaging part, raise packaging specifications and check Master Batch Packaging records from Central Pharma Support Team with the process of movement of goods for products and materials through SAP system, including, purchasing, receiving, moving from site to site etc. 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 »
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 »
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 »
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 »
brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects more »
