26 to 50 of 115 Pharmaceutical Jobs in the East of England

depending on qualifications and experience. Requirements: Experience within a similar role HNC/HNC/C&G/NVQ industry relevant qualification Ideally Pharmaceutical background About the company: I am working with a leading facilities... more »

industrial chemistry lab but would like to develop your skills further in a GMP environment? SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst – Level 1 Synergy, part of SRG, offer a range of scientific solutions to different … equipment or 5S standards. • Responsible for the safety of self and others within the Laboratory. Requirements: Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent, with up to 1-2 years practical work experience. Experienced in QC testing of finish drug products including HPLC for assay more »

opportunity to gain fantastic exposure in an industry GMP setting that will provide development and advancement opportunities. Whilst the duties may seem routine – testing pharmaceutical and personal care products using GC, HPLC and various wet chemistry techniques – the environment will offer the opportunity to fine tune and learn new skills … Experience in some of the following will be important – HPLC, GC, UV, FTIR A solid foundation of wet chemistry skills Degree (or equivalent) in pharmaceutical sciences, chemistry or an associated subject This business is not registered to offer sponsorship at this stage. For further information, please contact Mark Bux-Ryan. … qc, analytical, chemistry, HPLC, chromatography, GC, gas, high, performance, liquid, testing, product, raw, materials, pharmacopoeia, FTIR, UV, bench, laboratory, analyst, technician, GMP, GLP, manufacturing, pharmaceutical more »

Role: Senior Project Manager Location: Baldock, Hertfordshire Sector: Built Environment – life sciences, commercial fit-out Salary: £65,000 + £4,000 car allowance, bonus, pension, healthcare Carriera is proud to partner with a consultancy that has become a market disruptor more »

Information This Business Development Associate (BDA) opportunity is to support the Clinical Trial Division in the Bioservices (bio repository) and transportation team within the Pharma Services Group (PSG) of Thermo Fisher Scientific. Candidates with previous experience within Bioservices, Biobank, cold chain storage, transportation or logistics would be suitable for this … life sciences industry. This individual will seek to uncover new opportunities within the specific service areas of BioServices (bio repository) and transportation in the Pharma Services Group. The BDA will work within the territory of multiple Account Executives (AEs) to drive new growth opportunities supporting not only the growth of … and Safer place. What will you do: Research, identify and qualify BioServices (bio repository) and transportation opportunities within our given territory for fit with Pharma Services Group (PSG) Reach out and engage potential client companies with a targeted message about PSG and how we can add new value to their more »

I am genuinely excited to be working with a cutting edge Biotech who work at the interface of engineering and cell biology to develop human biomimetic platforms for the testing and development of therapeutics for serious human diseases. They are more »

cell therapies for cancer treatment? 𝐖𝐡𝐲 𝐡𝐞𝐫𝐞? You'll be joining an organisation that has earned a reputation for excellence within the IT and pharmaceutical sectors. Be inspired by the collective expertise and shared commitment to transforming cancer treatment. This position offers excellent opportunities for professional growth and development as more »

protocols and SOPs. Troubleshooting and maintenance of HPLC instrument. Your Background: PhD in Chemistry or related scientific discipline with significant experience working in a pharmaceutical or biotech environment. A background in polymer Chemistry combined with extensive expertise in Chromatography and spectroscopy to quantify genetic material loaded inside polymeric particles. Practical more »

Technologies designs and manufactures innovative industrial printing and laser coding equipment used to mark batch info and consumption dates on packaging within food & beverage, pharmaceutical and related sectors. Based 3-4 days a week at the Linx HQ in PE27 5JL, the Validation Engineer will be part of a small more »

SME and leader at respective program and business data forums Education, Qualifications, and Experience Essential Strong understanding of the indirect tax business process in pharmaceutical settings and tax touch points in E2E supply chain Analysis and interpretation of indirect tax (VAT,GST etc) requirements for domestic, free trade zones, exports more »

the Enterprise domain. • Champion the design for Tax capability through the appropriate governance forums Essential: • Strong understanding of the indirect tax business process in pharmaceutical settings and tax touch points in E2E supply chain • Analysis and interpretation of indirect tax (VAT,GST etc) requirements for domestic, free trade zones, exports more »

data strategy through risk assessments related to data management This role is for you if you possess: data management experience within the Biotech/Pharma/CRO sector understanding of clinical database structures, programming languages and data standards knowledgeable in Good Clinical Data Management Practices and relevant regulations ability to more »

rich blend of expertise in Clinical Development, Clinical Trial Supply, and Early Access Programmes, this organisation offers a unique and seamless service to its pharmaceutical and biotech clients. Your Role as RWE Manager In this pivotal role, you will: Lead and manage projects involving Real World Evidence (RWE), integrating these more »

changing treatments need life-improving product support to match, because when you put the two together, great things can happen. We are a pioneering pharmaceutical company, reimagining how drugs and services can benefit patients with rare disease to make their lives easier and improve their quality of life. Cycle, as … and healthcare professionals to understand the unmet needs of patients and their carers. By collaborating with academic communities and using the latest cutting-edge pharmaceutical technologies, we translate innovations into medicinal products that patients and caregivers actually desire. We deliver the required medicine with the minimum impact on daily routines … and, just as importantly, provide individualized support services to patients, families, carers and the healthcare professionals community. Cycle has three core areas of pharmaceutical development and work across rare metabolic, immunological and neurological genetic conditions: improving drugs – optimizing an existing drug; repurposing drugs – creating a new indication for an existing more »

ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with … in Engineering or a related field. Minimum of 5 years of industrial experience in CQV roles. At least 2 years of experience in the pharmaceutical industry. Strong understanding of industry regulations and standards. Excellent analytical and problem-solving skills. Effective communication and interpersonal skills. Ability to work effectively within cross more »

ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with … in Engineering or a related field. Minimum of 5 years of industrial experience in CQV roles. At least 2 years of experience in the pharmaceutical industry. Strong understanding of industry regulations and standards. Excellent analytical and problem-solving skills. Effective communication and interpersonal skills. Ability to work effectively within cross more »

of Quality Full-time Permanent Hybrid Salary: Negotiable based on experience Novumgen – the group of Entrepreneurs and Scientists. Novumgen is a diverse, integrated specialty pharmaceutical and biological company focused on investing, developing, manufacturing, and supplying innovative products that benefit patients and prescribers. We are focused on delivering life-changing medicines … Novumgen has made a lasting commitment to patient safety, introducing new products to our portfolio while maintaining unrivaled quality and exceptional service to the pharmaceutical industry. We are currently looking to recruit a Head of Quality this role is rudimentary and requires excellent knowledge and communication skills to ensure a … is on a growth trajectory, and we are looking for candidates who align with our purpose, have an entrepreneurial mindset, and want to impact pharmaceutical research. You will join a friendly, dynamic, committed international team to deliver consistent results to tight deadlines . Job Summary The Head of Quality is more »

and personal development. Job Summary We are seeking an experienced Engineering Project Manager with a strong background in industrial project management, particularly within the pharmaceutical industry, to join our team. As an Engineering Project Manager, you will be responsible for overseeing engineering projects from inception to completion, ensuring they meet … quality standards, deadlines, and budget constraints. Responsibilities Lead and manage engineering projects in the pharmaceutical industry. Collaborate with cross-functional teams to define project scope, goals, and deliverables. Develop detailed project plans, schedules, and cost estimates. Monitor project progress and make adjustments as needed to ensure successful project completion. Ensure … Engineering or a related field. Minimum of 5 years of industrial experience in engineering project management. At least 2 years of experience in the pharmaceutical industry. Strong project management skills with proficiency in project management software. Excellent organizational and multitasking abilities. Effective communication and leadership skills. Ability to work effectively more »

and personal development. Job Summary We are seeking an experienced Engineering Project Manager with a strong background in industrial project management, particularly within the pharmaceutical industry, to join our team. As an Engineering Project Manager, you will be responsible for overseeing engineering projects from inception to completion, ensuring they meet … quality standards, deadlines, and budget constraints. Responsibilities Lead and manage engineering projects in the pharmaceutical industry. Collaborate with cross-functional teams to define project scope, goals, and deliverables. Develop detailed project plans, schedules, and cost estimates. Monitor project progress and make adjustments as needed to ensure successful project completion. Ensure … Engineering or a related field. Minimum of 5 years of industrial experience in engineering project management. At least 2 years of experience in the pharmaceutical industry. Strong project management skills with proficiency in project management software. Excellent organizational and multitasking abilities. Effective communication and leadership skills. Ability to work effectively more »

Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that more »

Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants more »

Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants more »

Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants more »

Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants more »

Cambridge Up to £600 per day – Outside IR35 We are seeking a dynamic and detail-oriented Data Analyst to join our client in the pharmaceutical sector. This is a 6-month contract role with the possibility of extension and/or permanent placement at the end of the project. This … trends and best practices in knowledge management and information architecture. Ideally, your skills and experience will include: Ideally from a highly regulated industry i.e. pharma, finance, public sector etc. Demonstrated expertise in knowledge management, information architecture, or a relevant discipline. Solid grasp of taxonomy, metadata, and ontology principles and their more »