Biotechnology

  • Lab Manager R&D 7/16/2019 12:00:00 AM

    Salary: £0 Location: netherlands- delft

    My client is a ground-breaking biotech company using advanced tissue engineering to revolutionise the food sector. Due to consistent growth in the company, they are now looking for a driven, organised and proactive individual to run their labs. The successful candidate will work closely with the science team and the Head Scientist on making sure the lab is run smoothly, the atmosphere is good and everybody can focus on their respective expertise. You will spend your time on a diverse set of activities such as setting up new cell and molecular biology methods, writing and implementing standard operating procedures, procurement and maintenance of laboratory equipment and consumables. You will support the team by executing experiments ranging from culturing cells to media development and tissue engineering. Their culture encourages everybody on the team to actively shape their position and they provide ample opportunities for personal and professional growth. So, if you love the lab and want to put your brainpower towards aiding the development of world-changing research, please apply; What you will need • BSc, Masters or relevant qualification in the Biological Sciences • Significant experience working in R&D laboratory management • Experience culturing iPSCs • Experience in cell and molecular biology assay development What you will get • Excellent Career Development opportunities • Highly competitive salary • Great Benefits Package This a great opportunity for a driven individual wishing to develop their career in a thriving, multidisciplinary and dynamic team. Get in touch today to ensure that you don’t miss out!

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  • QA Specialist (Supplier Assurance) 7/16/2019 12:00:00 AM

    Salary: £0 Location: Motherwell

    My client is a ground-breaking biotech company developing and commercialising innovative cell-based products to treat disease, improving patient health and Quality of Life. They use novel immunotherapy to develop cell-based treatments for cancer and severe viral infections. Due to continuous growth in the company, my client is now looking for a driven, organised and proactive individual to join their team as a QA Specialist (supplier assurance). The successful candidate will enjoy a diverse role performing quality assurance activities relating to product support for the manufacture, packaging, testing, storage and distribution of manufactured drug products; ensuring they are compliant with current GMP and company expectations. My client’s unique culture, values and working environment attracts, retains, and inspires people to give their best. So, if you have an affinity for quality assurance and want to put your brainpower towards aiding the development of world-changing research in a dynamic team environment, please apply; What you will do: • Managing vendor approval system • Maintaining vendor files electronically and physically • Managing supplier performance and liaising with suppliers to complete investigations (vendor complaints) into supplier material defects • Progress and manage vendor change notifications ensuring the correct departments have assessed the applicable changes • Maintaining and updating vendor SOPs • Aid in the completion of technical agreements • To assist the Quality department in the overall implementation of the Quality function necessary for the maintenance of the quality management systems and related activities • Provide general support to all Quality Unit activities relating to GMP, GCP, and other similar Quality Systems established within the company • Identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems • Provide input into the enhancement of quality policies, systems and procedures as appropriate What you will need: • Minimum 5 years’ experience working within QA • Demonstrable experience and good knowledge of GMP regulations and vendor management • Strong follow-up skills and attention to detail • Ability to work independently • Excellent interpersonal skills • Strong time management and organisational skills What you will get: • Great Benefits Package including 32 days paid holiday allowance • Highly competitive salary This a great opportunity for a driven individual wishing to develop their career in a thriving, multidisciplinary and dynamic team. Get in touch today to ensure that you don’t miss out!

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  • QA Specialist 7/16/2019 12:00:00 AM

    Salary: £0 Location: Motherwell

    My client is a ground-breaking biotech company developing and commercialising innovative cell-based products to treat disease, improving patient health and Quality of Life. They use novel immunotherapy to develop cell-based treatments for cancer and severe viral infections. Due to continuous growth in the company, my client is now looking for a driven, organised and proactive individual to perform quality assurance activities and ensure compliance to their Standard Operating Procedures. The successful candidate will enjoy a diverse role that will require a hands-on operational approach, and at the same time influence strategic decisions together with coordinating wide-ranging process improvement projects. Their unique culture, values and working environment attracts, retains, and inspires people to give their best. So, if you have an affinity for quality assurance and want to put your brainpower towards aiding the development of world-changing research in a dynamic team environment, please apply; What you will do: • Issuing accurate creation/revision of documentation • Maintaining/updating Documentation Controls tracking tools and indices to ensure proper tracking of all SOPs/controlled documents/Change controls in the routing/approval process and batch record issuance in line with the Quality Management System (QMS) • Coordinating with Quality Assurance to ensure that all documentation affecting the production schedule is completed prior to issuance of batch records • Assisting Quality in the development, collating and reporting of key quality metrics to drive a culture of continuous process improvement such that it is fully compliant with current applicable regulations and quality requirements • Completing accurate and timely reviews of all documentation within the company and ensure all documentation is current, accurate and on schedule • Actively participating in internal and external audits, where required • Following Health and Safety practices, policies and procedures at all times • Performing other duties, as assigned, or as business needs require What you will need: • Minimum 5 years’ experience working within QA • Excellent oral and written communication skills, with the ability to proofread • Experience with Scientific and/or Pharmaceutical terms • Experience working to GMP and related practices for the manufacture of active pharmaceutical products • Excellent interpersonal skills • Strong time management and organisational skills What you will get: • Great Benefits Package including 32 days paid holiday allowance • Highly competitive salary This a great opportunity for a driven individual wishing to develop their career in a thriving, multidisciplinary and dynamic team. Get in touch today to ensure that you don’t miss out!

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  • Interim QA Specialist- Project Support 7/15/2019 12:00:00 AM

    Salary: £0 Location: Stevenage

    The Client: My client was established in 2012 as an independent centre of excellence to advance the growth of the UK cell and gene therapy industry, by bridging the gap between scientific research and full-scale commercialisation. We offer leading-edge capability, technology and innovation to enable companies to take products into clinical trials and provide clinical, process development, manufacturing, regulatory, health economics and market access expertise. Our aim is to make the UK the most compelling and logical choice for UK and international partners to develop and commercialise these advanced therapies. They are currently looking for a QA Specialist – Project Support, who will be responsible for providing oversight and subject matter expertise to the expansion phase build project as a key member of the wider project team. Reporting to and with the guidance of the Head of Quality Assurance, this role will ensure that the manufacturing centre, via proactive engagement, meets the standards and expectations of two key stakeholders; the regulatory authorities and potential collaborators. Most candidates will have: - Degree in life science or similar - Sound knowledge of FDA regulatory requirements and global standards (ISO 9001) - Ability to manage multiple projects and prioritise workload - Good team player with organisational qualities - A passion for delivering excellence - Ability to evaluate situations and find solutions For more information about the role or for a chance to apply, please contact Philip at 0161 250 5049 or philip.adebiyi@wearenorthpoint.com and I’ll be happy to help

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  • Assay Scientist 7/9/2019 12:00:00 AM

    Salary: £0 Location: Wetherby

    My client is an industry leading life sciences company dedicated to providing Life Scientists with the high quality, unique and powerful tools they need to develop safe and novel diagnostics and treatments. Currently, the company are developing novel bio-therapeutics that will compete with monoclonal antibodies and antibody mimetics in the future of diagnostics and treatments. Due to recent expansion and growth, they are looking for a Assay Scientist to join their state of the R&D facility. Working in a state-of-the-art facility, you will be responsible for optimising and validating a range of in vitro assays (such as ELISA, cell-binding assays etc.) to support the characterisation and the validation of their technology in industry-standard assays. Main Duties and Responsibilities: + Perform routine molecular techniques for QC of targets prior to phage display. + Design, develop and validate assays including sandwich ELISA, agglutination assays, LFD assays, cell binding and cell-based activity assays. + Evaluation of assay requirements, timelines, quality and accuracy of the experimental data produced. + Comply with existing Standard Operating Procedures and validates new methods. + Line Management of Research Associates. + Produce scientific reports/presentations for internal purposes or external clients, where necessary. >>>>> You Will Have <<<<< + PhD + 1 year or more working in the field of biotechnology or MSc + 3 years or more working in the field of biotechnology or 5 years or more working in the field of biotechnology. + Strong technical skills including experience in SDS, WB, ELISA, flow cytometry, protein interactions. + A bold and innovative nature and a desire to be fully involved in driving the growth of the business. For more information on this opportunity, please call Robert Frame on 0161 923 8189 or send a direct enquiry to robert.frame@wearenorthpoint.com

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  • Scientists or Senior Scientists - Cellular Immunology 7/9/2019 12:00:00 AM

    Salary: £0 Location: Motherwell

    My client is an emerging cancer immunotherapy company developing cell-based treatments for cancer and severe viral infections. The company have a clear vision to make CAR-T a mainstream therapy for eradicating cancer. They are developing safer, cheaper, consistent and durable CAR-T drugs for haematological and solid tumours My client is currently expanding at their state-of-the-art manufacturing facility and are looking for a number of talented scientists at all levels applying expertise across cellular immunology. The successful candidate will apply their expertise across a number of practical skills including primary cell culture of immune cells, development of cell-based assays, multiparameter flow cytometry, and molecular biology. Experience of working with clinical samples or with infectious material would be advantageous. The successful candidate will have the following skills/experience: + Working with others in the team, develop, optimize and perform in vitro assays for characterizing the biological activity of novel CAR constructs in T cells across a number of assay formats including kinetic and end-point analysis. + Have significant experience in working with primary immune cells (practical experience of gamma delta T cells would be particularly advantageous) across a range of applications, including cell isolation, cell-based assays, and flow cytometry. + Have experience and understanding of cell culture (including of primary immune cells), cell-based assays and of flow cytometry. Practical experience of the ACEA xCELLigence RTCA system would be particularly advantageous. + Have knowledge of T cell biology and an awareness of the challenges in developing CAR-T cell-based therapies. + Have proven experience of leading on R&D projects with successful and timely delivery of milestones and be familiar with GxP procedures, ideally in a cell therapy context. If you would like to know more about the role then please directly email Robert Frame on robert.frame@wearenorthpoint.com or call 0161 923 8189 for a confidential chat.

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  • Senior Preclinical Scientist 7/8/2019 12:00:00 AM

    Salary: £0 Location: Shepherds bush

    Senior Preclinical Scientist – London- Permanent- Competitive salary My client is an expert within imaging sciences, based in London. A fantastic opportunity for an Senior Preclinical Scientist has become available and they are looking for driven and enthusiastic people to join a technologically impressive company. You will be responsible for contributing to the delivery of in vitro and in vivo imaging studies using established and novel in vivo, ex vivo and in vitro techniques and methodologies to support novel PET ligands evaluation. You will also be asked to supervise a small team of preclinical research assistants. You will need: • PhD. or equivalent in a relevant discipline (e.g Biology, Biochemistry, Pharmacology, Molecular Biology) • Excellent knowledge of relevant preclinical in vitro laboratory techniques and a willingness to support in vivo studies, (PIL preferred). Excellent salary Professional development opportunities, generous holiday allowance, private healthcare insurance and company benefits.

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  • Analytical Chemist 7/8/2019 12:00:00 AM

    Salary: £0 Location: Shepherds bush

    Analytical Chemist – London- Permanent- Competitive salary My client is an expert within imaging sciences, based in London. A fantastic opportunity for an Analytical Chemist has become available and they are looking for driven and enthusiastic people to join a technologically impressive company. You will be responsible for the QC method development and routine analysis of PET radiotracers, to support clinical and pre-clinical studies with in a GMP environment, using (but not limited to) HPLC, LC/MS, GC, IC and NMR. You will also be responsible for raising / investigating OOS results and deviations with in QMS You will need: •BSc/MSc or equivalent in relevant Scientific field. •Experience of working analytical laboratory experience. •Experience with short-lived radioisotopes preferable (especially carbon-11 and fluorine-18). •Good knowledge of analytical chemistry techniques including but not limited to: HPLC, LC/MS, GC, IC and NMR. •Good understanding and compliance with GMP. Excellent salary Professional development opportunities, generous holiday allowance, private healthcare insurance and company benefits.

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  • Formulation Scientist 7/8/2019 12:00:00 AM

    Salary: £30000 Location: Nottingham

    Formulation Scientist- Nottinghamshire – up to £30k Based in Nottinghamshire, my client is a market leader in biotechnology and clinical manufacturing. Due to continued growth they are looking for Formulation Scientist from to join their experienced drug development team. Working in state-of-the-art facilities, you will be involved in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. As a Formulation Scientist you will conduct formulation development work including pre-formulation and formulation characterisation whilst supporting development and validation of radiolabelling methods for clinical studies. You’ll transfer formulation and radiolabelling methods into GMP clinical manufacturing, with input on manufacturing protocols, validation criteria and other key parameters and write experimental protocol and reports You will have: A BSc, equivalent or higher in pharmacy or chemistry related discipline Biochemistry, Pharmaceutical Chemistry etc.) 6 months plus experience in formulation development (specifically in Solid Oral Dose and/ or Spray Dry) Experience of GMP would be an advantage Competitive salary (up to 30k – depending on experience) Generous benefits package, State of the art facilities Fantastic development opportunities All applicants must have the right to work in the UK.

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  • Regulatory Affairs Manager 7/8/2019 12:00:00 AM

    Salary: £0 Location: Nottingham

    The Client: My client is a pharmaceutical organisation dedicated to accelerating the drug development of new drugs for patients around the world. They provide formulation development, clinical pharmaceutical trials and clinical and commercial manufacturing services to the pharmaceutical and biotech industry. Their vision is to transform drug development with science and innovation and hence, operate from state-of-the-art manufacturing and clinical facilities in both UK and US. They are currently hiring for a Regulatory Affairs Manager at their site in Nottingham who will act as Regulatory Lead in providing a centralised service coordinating regulatory submissions (CTA applications, ARSAC applications & Research Ethics Committee (REC) submissions) for clinical studies conducted by the company. As the Regulatory Affairs Manager, you will drive continuous quality improvement relating to regulatory processes. Most candidates will have: - Educated to a degree level in a biological or life science - 3 years’ minimum regulatory experience, preferably in a pharmaceutical company or CRO - Project leadership experience would be advantageous - Familiarity with CTA and REC - Confident and articulate communicator - Previous interaction with regulatory authorities would be an advantage - Experience in IND and eCTD submissions is highly desirable but not essential In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.

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