76 to 100 of 149 Permanent Pharmaceutical Jobs in the South East

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. JBRP1_UKTJ more »

Our Client develops and distributes innovative, high-value specialty pharmaceutical products. They are now seeking a Technical Specialist - Pharmaceutical QC and Manufacturing. This position is a full-time permanent role which will be office based in Surrey with blended (hybrid) working arrangements currently in place. Job Purpose Take day-to … current project process (trackers, classification of files etc.). Qualifications/Experience BSc or equivalent science-based degree Prior experience of working in a Pharmaceutical production or development environment, to include QC and working with staff on issues arising within a production environment. Familiar with the concepts of GxP systems … and other pharmaceutical terms and acronyms. Experience of managing Tech transfers, troubleshooting and product development of product change projects including process, analytical, planning, documentation, cost control and communication. Experience or ability to fill eCTD module 3. Ability to establish and maintain effective working relationships with internal and external stakeholders. Strong more »

complying will all relevant national and local legislation, regulations and guidelines in relation to GMP. Responsible for leading the implementing and maintaining of a Pharmaceutical Quality Management (PQS) System across all relevant areas of Pharmacy and monitor its effectiveness. To provide expert quality assurance to the Pharmacy Aseptic Services Unit … PASU) in the quality review of their products and processes to maintain a high quality pharmaceutical aseptic service. To ensure the delivery of a safe and efficient Aseptic Services Unit which meets all legal and professional standards. To facilitate and support the efficient and cost effective use of medicines across … we are proud to be rated good by the CQC. Visit our website to catch up on our latest news. Job description Job responsibilities Pharmaceutical Quality Management Systems Responsible for implementing the Pharmacys department PQS, critically assessing with view to maintaining a continuous quality improvement cycle and in response to more »

P/A Polar Speed has a reputation for quality, compliance, operational and customer facing technology and monitoring solutions in the growing temperature-sensitive pharmaceutical logistics market in the UK. The company specialises in active temperature-controlled deliveries to hospitals, pharmacies, wholesalers and medical care surgeries as well as to … end patients which it serves through its homecare business. Its customers include some of the best known pharmaceutical brands in the world. Due to an increase in business we currently have a new position in our Quality department based at our Leighton Buzzard HUB. Successful candidates must be eligible to more »

potential What you'll be doing: Responsible for actively leading, mentoring and supervising the QHSE requirements of the Veolia IFM operation on a client pharmaceutical manufacturing site. Maintains an up to date knowledge of Quality and H&S Regulations and advises Veolia management of implications for the site. Represents QHSE … respective CAPA plans Excellent Report/presentation writing skills Strong interpersonal and analytical skills Knowledge of cGMP regulations- desirable Experience of working in the Pharmaceutical or other regulated industry - desirable What's next? Apply today, so we can make a difference for generations to come. We're proud to be more »

IGES UK Pharma Ltd. is a new entity in the UK, and part of the IGES Group , set up specifically to offer strategic advice to clients for early trial planning and launch of new innovative medicines within the NHS system to secure reimbursement. In total, the IGES Group employs more … In collaboration with the wider IGES Group , the vision of the company is to provide a full service from strategy to submission for the pharmaceutical and biotech sector. As such the consultant has a vital role to lead client engagements through excellent communication, project management, and presentation skills. Besides, the … the company. Primary Responsibility: project delivery and Business Development activities in the Market Access space for existing and new named UK-local accounts of pharmaceutical and Biotech companies, working closely with the Director, and colleagues with delivery expertise in other functional areas and work closely with the Director on Business more »

QC Radiochemist/Analyst Working exclusively with an international advanced pharmaceutical company, I am currently supporting multiple hires within their QC team for one of the UK facilities based in South Yorkshire. These positions are hands on production scientists within a significantly growing area of radiopharmacy – however, no prior experience … shifts Must have own transport to access the site due to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

Job summary Exciting Opportunity: Project Manager at RMHRMH is seeking a highly skilled and experienced Project Manager to oversee multiple high-value projects across various clinical and non-clinical settings. The successful candidate will be responsible for managing projects from more »

The chemical biology team at EMBL-EBI delivers world-leading databases and resources to the scientific community. Our flagship resource, ChEMBL , is a database of high-quality quantitative small-molecule bioactivity data curated from the scientific literature and direct data more »

Are you an experienced Pharmaceutical Automation Project Manager seeking a new challenge in the Pharmaceutical industry? If so, look no further! We have an exciting opportunity available to join a blue-chip Pharmaceutical organisation as a Automation Project Manager in the Process Engineering department. You will ensure that operations are … Ideal Requirements for Automation Project Manager You will be a seasoned Project Manager, with experience of managing Automation projects end to end within the pharmaceutical industry. Experience of setting up SMART factories. Experience of working with automated systems and digitised manufacturing. Proven use of connected devices and machinery and production … operational technology (OT), automation systems and innovative proof-of-concept (POC) initiatives. Responsible for secure and compliant control systems aligned to industry standards and pharmaceutical GAMP guidance. Recruitment Process 2/3 stage interview process. Excited to learn more? Click apply, or reach out to Claire Handley for full details more »

Quality Assurance Officer- Batch Release – Global Pharmaceutical Company Contract: 12-Month Contract Location: Marlow, UK Salary: £32,000 p/a Working Pattern: Hybrid SRG are working with a Global Consumer Pharmaceutical company to help them find a Quality Assurance Officer to join their busy team. Reporting to a Quality … scientific discipline with relevant experience (Preferably Biology/Chemistry/Pharmacy/Life Sciences) 2-3 years in a GMP environment Basic experience in pharmaceutical manufacturing, distribution, and control measures Basic experience in Quality administered systems. Previous use of TrackWise® QMS beneficial. Experience in operating in a QMS. Experience in more »

the platform administrator. - Stay updated on current requirements for serialization and aggregation, advising colleagues accordingly. Key Skills and Requirements: - Strong technical expertise in the pharmaceutical industry, specifically in the manufacturing and serialization of medicines. - Proven project management experience. - Excellent problem-solving skills and attention to detail. - Experience working with databases … have any questions, please contact Ingrid Aymes on 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 »

departments. We require a Chief Technician to join the QA team to be responsible for the implementation and maintenance of all aspects of the Pharmaceutical Quality System (PQS) system. You will have previous experience working as senior within Quality Assurance, while supporting the manufacture of aseptically prepared products, either within … the NHS or within the pharmaceutical/life science industry. This position supports the Quality release of product to wards and customers. Main duties of the job The post holder will manage the quality systems to ensure product quality and ensure patient safety is maintained.This position will deputise for the … Job description Job responsibilities The Chief Pharmacy Technician for Quality Assurance (QA) is responsible for the implementation and maintenance of all aspects of the Pharmaceutical Quality System (PQS) system.The post holder will manage the quality systems to ensure product quality and ensure patient safety is maintained.This position will deputise for more »

Project Manager | Permanent | Hybrid - Oxford | Circa £65k We are currently working on a new Project manager position at a super exciting pharmaceutical startup client based in Oxford. They are looking for someone to come and drive Good Clinical Practice (GCP) principles, who can come in and build relationships with key … stakeholders in order to keep the quality team moving forward. The ideal person will have strong QA experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup environment. This individual will also be a fantastic communicator, comfortable … key stakeholders across the business Report up to senior leadership and represent QA in reporting What you will bring: Previous project management experience within pharma/biotech or similar Outstanding knowledge of GCP, TFA and FDA regulations Strong project management principles, key knowledge of agile methodology A desire to be more »

successful candidate will lead on a portfolio of cancer & non-cancer clinical trials undertaken within ESHT. They will appraise all relevant clinical trials & offer pharmaceutical input in accordance with legal requirements & Good Clinical Practice (GCP) relating to the prescribing, handling, dispensing, administration, storage & disposal of investigational medicinal products (IMPs) & non … provision, management and development of a high quality, comprehensive specialist clinical trials pharmacy service. 2. To develop, implement and monitor a strategy for the Pharmaceutical Clinical Trials service within the Pharmacy Directorate. 3. To be the lead pharmacy contact for clinicians carrying out pharmaceutically based clinical trials and to provide … Cancer and or Aseptic Services Experience in utilising information technology within the workplace including inputting, retrieving information and producing reports Experience in managing the pharmaceutical element of clinical trials. Desirable Has experience in policy, procedure development. Previous experience in mentoring and training pharmacy staff Has previous Line management experience Disclosure more »

will be completing their clinical pharmacy diploma's/MSc's shortly. Main duties of the job Key roles include: Delivery of high quality pharmaceutical care to adult cancer in-patients, day-case, and out-patients. Participation in pharmacy services to the Day Treatment Unit to optimise patients' medication and … the most cost-effective choice of therapy To participate in ward rounds, clinical meetings or out-patient clinics as appropriate in order to provide pharmaceutical advice to prescribers and other health care professional To liaise with external agencies to ensure safe, timely and appropriate supply to patients e.g. Baxter, Homecare … current working practices. Person Specification Clinical Pharmacist (Cancer) Essential Qualified to a degree level (4 year MPharm or equivalent) and Pharmacist registration with General Pharmaceutical Council (GPhC) Diploma/MSc in Clinical Pharmacy or equivalent experience Experience of working as a clinical pharmacis Problem identification and solving skills Well organised more »

Role: Supply Chain Serialisation Manager Type: Permanent Location: Surrey I am currently working with a client of mine who are are a rapidly expending pharmaceutical company and are currently looking for a Serialisation Manager who will be responsible for the compliance of the groups products with diverse national serialization requirements … aiming to safeguard patients from falsified medicines. We've helped this Pharma with over 30 hiries in the last 12 months and are continuing to support their growth across the UK and EU. Responsibilities: Ensure the proper functioning and operation of the serialisation solution platform by coordinating with the provider … 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 »

for use in hospital and at discharge. Please see Job Description and Person Specification for full details. Person Specification Application Essential NVQ Level 3 Pharmaceutical Sciences or equivalent Accredited Checking Pharmacy Technician Registered as a Pharmacy Technician with General Pharmaceutical Council (GPhC) Significant experience in hospital management post qualification Experience more »

M+E Package Manager - Pharmaceutical Cleanroom Project Embark on a pivotal role in the construction of a state-of-the-art Grade 3 cleanroom facility in the greater Stevenage area. This high-profile pharmaceutical project is looking for an experienced M+E Package Manager with a focus on HVAC and ductwork systems … designs and ensure compliance. What You'll Need: Proven experience as an M+E Package Manager, with a background in HVAC and ductwork installations for pharmaceutical/cleanroom/data centre/food manufacturing facilities Knowledge of HVAC systems, ductwork design, and cleanroom environmental control systems Proficiency in project management software … What You'll Receive: Competitive remuneration package commensurate with experience - Permanent or Contract arrangements available Opportunity to contribute to the delivery of an advanced pharmaceutical facility with cutting-edge HVAC and cleanroom systems Chance to work with a dedicated, quality-driven project team on a high-profile assignment. If you more »

level requirements into amazing user experiences. You’ll be based remotely, or in our Sandwich office. At YPrime, we help our clients in the pharma and biotech industries to collect data from patients using mobile devices, assign patients to study treatment groups and dispense clinical trial drugs and supplies using … better! Team spirit; strong communication skills to collaborate with various stakeholders Good time-management skills Understanding or prior experience in the clinical trial/pharmaceutical industry is an advantage Here are some more details about the job: You’ll gather and evaluate user requirements in collaboration with product managers and 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 19,000 staff … values their staff and puts an emphasis on career development. What makes this opportunity special? You will be 100% client focused with a prestigious Pharmaceutical Company You ll be working in some cutting edge therapy areas, particularly within Oncology Career progression can be exceptional because there are lots of studies … Key words: Clinical Research, SCRA, Clinical Research Associate, London GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Oncology, Field Based, Home Based, CRO, Pharmaceutical, London Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is more »

Graduate Marketing and Software Operations Support Location: Rural Ashford Salary: £23k - £26k DOE Due to the clients rural location you must have your own transport. Do you have experience in Software and Marketing and are looking to advance your career more »