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 »
Slough, England, United Kingdom Hybrid / WFH Options
Parkside Recruitment
is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of 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 »
enable our clients to meet the changing needs of the global landscape. Required Understanding of Supply chain planning domain, preferably in Life Science or Pharma Industry Have multiple cycles of leading implementation experience in complex supply-chain solution design, development, and testing. With at least, 1 full cycle Kinaxis implementation 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 »
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 frameworks such as, Lean Six Sigma, ITIL V4, GDPR, ISO27000, ISO27001. Cyber Essentials more »
Royston, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
Electrical Engineering You have experience in electrical product design and development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical more »
Royston, England, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
Electrical Engineering You have experience in electrical product design and development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical 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 »
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 »
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 »
and gene synthesis applications. Yourgene also has a global laboratory service network equipped to be a full life-cycle partner for clinical, research and pharmaceutical organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory approval and commercialise new products and services. In 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 »
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 »
solving skills and attention to detail Effective communication and collaboration skills Ability to work independently and as part of a team Knowledge of the Pharma or healthcare industry is a + What we offer Integration in a highly qualified, successful and ambitious team International Startup feeling in the heart of more »
On behalf of our Global pharmaceutical client here are RED we are looking for a Senior Functional Consultant Treasury owns the technical solution design for the Treasury capability or part of a cross functional component The role is a key position on the customers Programme IT design team taking a more »
recognised management consultancy firm that contributes to strategic decisions, tailored to a wide range of external stakeholders in the global healthcare space, such as pharmaceutical, biotechnology, digital health, and medical devices. With a clear career progression and personal development plan in place, you are guaranteed to be set up for more »
Milton Keynes, Buckinghamshire, South East, United Kingdom Hybrid / WFH Options
Insite Public Practice Recruitment
k for 6 Months, Milton Keynes An exceptional 6-month contract opportunity has arisen with a leading innovative pharmaceuticals business that pioneers quality pharmaceutical products across the EMEA region. They are seeking a qualified Interim FP&A lead to join their renowned Product and R&D divisions. In this pivotal more »
and regulatory standards. Qualifications: Minimum of a Bachelor's degree in Engineering or related technical field. Proven experience as a CQV Engineer in the pharmaceutical or biotechnology industry. Strong understanding of industry regulations and guidelines. Excellent technical writing and communication skills. Ability to work independently as well as part of more »
to influence peers and exec-level staff. Good knowledge of IBM Maximo is required along with hands on experience working in industries such as Pharmaceutical, Oil and Gas, Facilities Management, manufacturing or Travel and Transport. PLEASE NOTE that sponsorship is not available for overseas candidates. more »
to check that products remain safe, compliant and of a high standard for supply. Qualifications, Experience & Knowledge Required: Proven Quality Assurance experience in the pharmaceutical industry, with a solid foundation in QA principles. Strong analytical skills and keen attention to detail to identify and address potential quality issues. Proficient writing more »
support to internal teams and external partners. Requirements Bachelor's degree in a relevant scientific discipline. Experience in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with more »
CMOs) Develop knowledge and create IP opportunities for the portfolio Requirements Minimum 8 to 10 years’ experience as a drug project manager in a pharmaceutical and/or biotech company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late more »
