101 to 125 of 178 Permanent Pharmaceutical Jobs in the South East

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 »

Company Description We are an innovative, technology-oriented strategy consultancy founded by consultants and professors from leading business schools in Europe. 3HORIZONS are the creators of Strategy in Action (SiA), an innovative end-to-end strategy programme designed to empower more »

Job summary Royal Marsden NHS Foundation Trust is looking for an experienced & passionate Infrastructure & Systems Engineer to join the RM Digital Services team (RMH Digital). This is an exciting opportunity for a highly motivated & professional individual to join the more »

act as a Pharmacy point of contact for all clinical trials, for both internal and external enquiries. To maintain professional registration with the General Pharmaceutical Council and to undertake continuous professional development (CPD). Person Specification Qualifications and Training Essential NVQ Level 3 Pharmacy Services, BTEC Pharmaceutical Sciences or equivalent … Registered Pharmacy Technician with the General Pharmaceutical Council Accredited Checking Pharmacy Technician (ACPT) qualification Desirable GCP training Skills and Experience Essential Good understanding of Clinical Trials Experience of working in a hospital pharmacy Evidence of working in a team - Effective team player Good IT skills - Knowledge of Word and Excel more »

really value their employees. We are looking for someone who has a track record in Leading the HSE function across multiple companies in a Pharmaceutical environment. It is key that you have experience within a GXP/GMP environment. Purpose of the Job Health, Safety & Environment Lead and provide oversight … and Global strategic leadership covering health, safety, and environment across the Pharmaceutical account. To co-ordinate, as the single source of accountability, country/regional HSE staff, global subject matter experts and account dedicated/supporting resources to support & advise the operational teams working on the account in accordance with … mobilize business leadership to reach and sustain such a leading culture. Candidate should have a solid grounding and practical experience in working in the Pharma environment and facilities management areas. The candidate must also have a strong skill set to deliver tactical and strategic thinking in the application of HSE 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 »

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 »

Job Title: Data Engineer Job Type: Permanent Location: London or Fully remote Salary: £50,000-£70,000 (Dependant on experience) + Bonus + Benefits Skills: Python, SQL, Posgress SQL, Snowflake, Powershell Roc Search`s client provides real-time decisions and more »

customer-facing and technically focused application Implementation Consultant focused on Oracle SQL scripting, is required by leading international SAAS/Software Provider in the Pharma/Life Sciences domain who's used by the majority of the worlds top 20 Bio-Pharma companies for rapid drug discovery. This role is … UK Driving licence Desirable skills for the Technical Implementation Consultant would include Implementation of SAAS/Cloud-based software. Experience in Life Sciences/Pharma software/Laboratory/Lab systems/Lab Informatics/Compound management such LIMS, LIS, LMS, Lab Sample Management Lab Automation, Liquid Handling, Lab Robotic … This is an outstanding chance to join an international software company whose software is used by the majority of the worlds top 20 Bio-Pharma companies and whose software integrates with Laboratory Sample Management/LIMS software for pharmaceutical and biotech laboratories with robotic automation systems (liquid handlers, automated stores more »

CRC Press Rights Manager, the sales executive will be responsible for maximising revenue by licensing content from Biomedical Science, Healthcare, Life Science, Medicine, Veterinary & Pharmaceutical portfolio. Experience within a medical/pharma sales environment would be beneficial. This role is offered on a maternity contract basis of 9-12 months more »

Quality Assurance (GCP) Location: Central London (4 days on site) Type: Full-time, Permanent A renowned organisation specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks a dedicated Head of/Director Quality Assurance. Embracing a culture of excellence and innovation, we are committed to advancing medical … and train other QA personnel, effectively managing workload distribution and monitoring task completion. Qualifications and Experience: Proficient knowledge of Quality Assurance principles within the Pharmaceutical Industry. Strong understanding of Quality Management Systems in the pharmaceutical sector. Thorough familiarity with ICH-GCP and GMP guidelines. Experience in hosting Sponsor audits and more »

Product Surveillance Reporting Analyst 12 months £17.96 p/h Marlow – hybrid (3 days on site) SRG are partnered with a pharmaceutical organisation who are seeking a Product Surveillance Reporting Analyst to join their team in Marlow. Purpose of the role The Reporting Specialist is responsible for executing all of … scientific background • 5+ years of work experience in a cGMP related industry or in a clinical setting (preferred) • Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products. • Knowledge of FDA Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred. more »

Job: Tendering Specialist Job Location: Maidenhead, Berkshire Company: A Global Pharmaceutical Company CPL Life Sciences is working exclusively with a global pharmaceutical client that work on life-changing technologies with leading businesses and products in diagnostics, medical devices and nutritional. My client is looking for a Tenders & 3rd party Specialist 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 »

while growing their careers. Join our global team and grow with us. Job description: Are you a Field Service engineer working primarily in the pharmaceutical or biotechnology industry? Do you have strong electrical and mechanical knowledge? If so, this could be a great opportunity to join us in our LPS … Sales Help customers and get feedback from them Required profile: A qualification in mechanical, electrical, mechatronics, bioengineering Experience as a service engineer in the pharmaceutical or biotechnology industry Experience working on capital or robotic equipment would be beneficial Strong customer service skills and great communication skills Ability to adapt to more »

skills, including CI/CD pipelines. The Azure Cloud Architect will play a crucial role in designing, implementing, and maintaining cloud-based solutions for Pharmaceutical clients. Skills Required: Architect level Experience in Azure Cloud platforms. Experience with DevOps roles and CI/CD pipelines. Ability to contribute to DevSecOps development … Lake, Azure Data Factory Bachelor’s or Master’s degree in Computer Science, Information Technology, or a related field. Experience working in healthcare or pharmaceutical industry. Proficiency in Azure Cloud environments, Azure Data Lake, Azure Data Factory, Microservices architecture. Knowledge of Azure DevOps, CI/CD pipelines, GitHub, Kubernetes (AKS more »

Role: Clinical EHR Testing & Implementation Analyst Location: Hybrid, United Kingdom Contract: FTC 12 – 18 months About us: CereCore was formed in 2001 as a shared service business within a large hospital operator. We focus solely on helping healthcare organizations align more »

Cloud Engineer Are you ready for what’s next, now? We’re looking for a Cloud Engineer in our Dorking office in. The position is 4 days per week and office based. You’ll join an awesome team to support 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 »

HPLC Analyst Are you passionate about contributing to the advancement of pharmaceutical science? Do you possess expertise in HPLC analysis and thrive in a dynamic laboratory environment? If so, we have an exciting opportunity for you to join a thriving Guildford based team! Position: HPLC Analyst Location: Guildford, UK Shift … Shift work required Transportation: Ideally, candidates will have access to their own vehicle Key Responsibilities: Perform HPLC analysis on pharmaceutical samples in accordance with established protocols and procedures. Maintain accurate records of experimental data, results, and observations. Collaborate with cross-functional teams to support research and development projects. Ensure compliance … with regulatory standards and safety protocols. Qualifications and Skills: Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, or related field. Proven experience in HPLC analysis within a pharmaceutical or analytical laboratory setting. Familiarity with chromatographic techniques, instrument troubleshooting, and data interpretation. Strong attention to detail and ability to work more »

SRG are currently looking for Regulatory Artwork Implementation Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory team on an initial 12 Month basis to be based at their offices in Kent (hybrid). The Role: Responsibility for tracking and real-time transparency of … content of labeling updates and raise issues with the EU ALIM Lead and the Regulatory Strategists. Develop and maintain relationships with relevant stakeholders. Use pharmaceutical packaging and artwork knowledge/experience to collaborate with Manufacturing Artwork Centres. Interact and follow up with all Market Approvers as needed, and re-direct more »

empowering Africa to meet the healthcare needs of its rapidly growing population. Our network will be designed to catalyse Africa's self-sufficiency in pharmaceutical and vaccine R&D and manufacturing, ensuring the continent can drive its own health innovation agenda. We will establish digital and clinical infrastructure, while prioritizing … an organisation that will transform lives for generations to come. Qualifications include: 15+ years of experience in operational leadership roles, ideally in the CRO, pharmaceutical, or academic research sectors; experience in start up environments a plus Track record of successfully scaling organizations, with experience managing budgets of $20M+ Deep expertise more »