Jobs

We found 79 job(s) for you:

  • Territory Manager

    Salary: £0 Location: BIRMINGHAM

    The Client Specialists in producing highly sensitive and specific antibodies for the detection of certain cancers, my client provide in-vitro diagnostic test kits to hospitals and clinical laboratories globally. My client is moving from strength to strength and have now established themselves as the world leading company for this area of clinical testing with global revenue exceeding £80,000,000 in their previous year. The Role A customer interfacing sales role to support the Regional Business Manager in delivering the regional sales target. Territory will be South East (Oxford, Berkshire, Surrey, Sussex, Kent, London (south of the river) Your responsibilities will include: • Decision making, organisational responsibility and accountability for their Territory. • Develop strong customer relationships with allocated customers. • Full responsibility for their role and/or projects within the department on a day to day basis. • Manage own workload to meet the departments objectives and targets. • Will be motivated to drive your area of responsibility forward and achieve targets set. • Maintain confidentiality in Company and employee matter. • Write, review and control documents and deliver them on time. • Communicate effectively to all internal stakeholders and Sales team. • Pro-actively problem solve. • Provide timely feedback to the Regional Business Manager from the field. • Conform to all organisational SOP including travel and expenses policies. Knowledge and Skills • Background in Biological Science or life Sciences (BSc qualified or above) • Knowledge of NHS, especially pathology laboratory • Experience of working within the NHS in one of the fields of Haematology, Immunology, Clinical Chemistry or Blood Sciences • Excellent communication (both written and verbal) • Excellent relationship building skills with internal and external Stakeholders • IT competent (Excellent working knowledge of Microsoft Word, Good working knowledge of Excel and PowerPoint) • Experience working in a sales role within an Immunodiagnostics company preferably involving exchanges with Immunology, Haematology and Clinical Chemistry laboratory stakeholders in the NHS The Candidate Highly self-motivated and highly organised with a passion to excel in your work. You will have experience in working to deadlines and motivating a team. You will need good analytical skills and excellent problem-solving skills, with experience managing and working with budgets and finance decision making. You must live on Territory – London (South of the river), Oxford, Berkshire, Surrey, Sussex & Kent. The Benefits • Bonus available of a potential £15,000 PA • Company Car • £200 to cover monthly expenses (Lunch, washing car etc) • Competitive Salary Salary is negotiable on experience ---- This is an opportunity to join a global leader in clinical testing, to be part of a professional team and make a tangible difference in real world medication. For more information and a confidential discussion, please contact Kieran Whittaker on the below: - Tel: 0161 923 8174 Email: Kieran.Whittaker@wearenorthpoint.com

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  • Regulatory Affairs Specialist

    Salary: £0 Location: BIRMINGHAM

    Regulatory Affairs- Biotech - Midlands - £40k My client is a leading international Medical Diagnostics business. Due to there continued expansion they are looking to hire a Regulatory Affairs Specialist. The ideal candidate for this position should have significant experience working within a global pharmaceutical company in the area of regulatory affairs. The successful candidate will benefit from; + £50k salary + Excellent Benefits Package + Great Career Opportunities

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  • QA Assistant Validation

    Salary: £0 Location: BIRMINGHAM

    The Client Specialists in producing highly sensitive and specific antibodies for the detection of certain cancers, my client provide in-vitro diagnostic test kits to hospitals and clinical laboratories globally. My client is moving from strength to strength and have now established themselves as the world leading company for this area of clinical testing with global revenue exceeding £80,000,000 in their previous year. The Role Working as a QA Assistant your responsibilities will include: • Ensuring all Equipment Qualification and Process Validation is carried out in line with Company Policy & Procedures. • To assist with Validation of IFS and other Software systems. • Generate User Specification Requirements (USRs), Validation Protocols/Reports to Company Standards. • Reporting any issues with Data/Results obtained and assisting in finding solutions. • Preparing and delivering documentation for validation projects. Ensuring validation is carried out to schedule, that any issues are reported in a timely fashion and that all documentation follows company templates. • Carrying out validation trials following Installation and Operation Qualifications protocols documented, and documentation of results. Reviewing and approving of the same documentation for other operators. • Carrying out Performance Qualification/Process Validation trials and documenting results. (Including appropriate data analysis). Knowledge and Skills • Working knowledge of FDA Part 820 and ISO13485 • Working knowledge of computer software validation, FDA Part 11 and GAMP5 • Experience of working within a Validation or Manufacturing Environment • Experience of working with IVDs or Medical Devices • Knowledge of cGMP • Good Data analysis skills • Good report writing skills The Candidate You will be open, friendly and professional with an excellent eye for detail. Having an inquisitive mind and the flexibility to cope with changing priorities would be advantageous. You will be able to understand and follow procedures and processes. Salary is negotiable on experience ---- This is an opportunity to join a global leader in clinical testing, to be part of a professional team and make a tangible difference in real world medication. For more information and a confidential discussion, please contact Kieran Whittaker on the below: - Tel: 0161 923 8174 Email: Kieran.Whittaker@wearenorthpoint.com

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  • Senior FPGA/Hardware Designer

    Salary: £0 Location: FULHAM

    Based in Central London, my client is a market leader in dataflow technologies. The company design their own custom hardware platforms for use within scientific measurements. Their hardware engineers are industry leading professionals and are responsible for developing and sustaining the internal operating system, software libraries and on chip IP. Selling to private companies and governments alike, this is a chance to join a company at the forefront of scientific tech. In order to join as a Senior FPGA/Hardware designer you will have experience in managing the design and delivery of complex systems from the early design stages to final installation in a production environment, interacting with key stakeholders and taking responsibility for delivery on time and within budget. You will need a degree or equivalent professional qualification in Electronic Engineering, Computer Science or a related discipline and experience in digital circuit design, preferably using VHDL for FPGAs. + Multi-layer PCB design and debug with FPGAs. + High-speed digital design (eg. QDR/DDR memory interfaces, PCI-Express, 10G Ethernet, Infiniband) + Product design and test experience (eg. EMC Compliance) + Systems/device driver programming for Linux in C. +Knowledge of object-oriented software techniques in Java or C++. Salaries are expected to be upwards of 65k for this role. If you are interested in hearing more, or submitting an application feel free to get in touch with a member of our team.

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  • Analytical Manager

    Salary: £0 Location: SHEPHERDS BUSH

    Based in London, my client is a global leader in specialist imaging working towards the understanding of disease and translational drug development. You will have- Minimum of BSc in Chemistry or other relevant subject with strong evidence of your analytical expertise Extensive experience in HPLC, GC, IC (LCMS would be beneficial but not essential) Strong people management skills Evidence of leading a team Due to company progression, they are looking for an experienced and time served Analytical manager. Reporting to the head of clinical chemistry, you will be responsible for leading a multidisciplinary team of 6 specialists with in a GMP facility, in analytical chemistry and microbiology. This position requires an individual to lead by example and demands someone with strong people management, technical expertise and effective communication skills. Excellent salary £45-£50k (dependant on experience) Great career progression options.

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  • Statistician

    Salary: £0 Location: BIRMINGHAM

    Statistician - Biotech - Midlands - £35-38k My client is a leading international Medical Diagnostics business. Due to there continued expansion they are looking to hire an experienced Statistician. The ideal candidate for this position should have significant experience working within biotechnology from areas such as varied as statistical design, experiment interpretation, result interpretation, assay development and DoE. The successful candidate will benefit from; + £30-33K Basic Salary + Excellent Benefits Package + Great Career Opportunities

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  • Group Leader - Cell Line Development

    Salary: £0 Location: OXFORD

    Group leader- Cell line development-Permanent-Oxford My client is recruiting for a Group leader-Cell Line Development My client is a specialised contract research organisation offering services to support the discovery, development and production of biologics, gene and cell therapies, they are based in Oxford and their products are are sold both directly and through a global network of distributors. Key responsibilities; Day to day management of activities within Cell Line Development laboratories Direct line management of CLD group To work closely with internal and external stakeholders to define project goals and deliverables, in line with planned project objectives To keep up to date with the scientific literature and developments in the field Support and contribute to protection and assessment of intellectual property Criteria; A Ph.D or DPhil in a relevant discipline, along with several years industry experience applicable to the role. Extensive knowledge of subject area, and ideally a strong network within academic and industry groups High-level attention to detail Experience in managing teams, both via direct line management and through matrix management Good understanding of regulatory requirements for the generation of cell lines for biomanufacturing

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  • Clinical Chemist Manager

    Salary: £50000 Location: BIRMINGHAM

    My client is a leading immunodiagnostic company based in the Midlands. With a successful medical diagnostic platform, this company are a place where career aspirations meet with a resoundingly positive commercial environment. Supporting Industry, healthcare professionals and hospitals, this company has both the drive and innovation to improve the lives of patients globally. The role is for a Team Leader in Clinical Chemistry; running a small team of clinical chemist professionals in terms of clinical studies, assay development and scientific support to the diagnostic division of the company. You will have; + A postgraduate degree in chemistry or biology related subject + Experience of working within the NHS + Accomplished electrophoresis scientist + Experience of SPE, IFE, FLC and Mass Spectrometry. If this sounds like the perfect opportunity for you – do get in touch on 01619238186 or contact me on adam.robinson@wearenorthpoint.com.

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  • QC Officer

    Salary: £0 Location: OXFORD

    The Client Based in Oxford, my client is an extremely successful gene and cell therapy company focussed on developing life changing treatments for serious diseases. They have expanded from around 80 people in 2014 to over 250 currently, and are continuing to expand due to a number of extremely high-profile contracts won over the last 18 months. As a result of this continued growth, they are currently looking for ambitious and dedicated Senior QC Analysts to manage an ever-growing quality department. The Role Working within a bio-pharmaceutical environment, youll be responsible for leading a dynamic team. As a Senior QC Officer, youll share your knowledge and experiences of working with Immunoassays and Molecular assays. Responsibilities • Over-see collation of data points from assay controls and product data to trend results, capture metrics leading to assay improvement and optimisation • Maintain QC databases, Certificates of Analysis and Product Specifications • Prepare assay performance reports and product reviews. • Ensure stability study are set up, performed within the time point window and reported in a timely manner • Issue test samples and control materials, prepare outgoing shipments and receive incoming shipments • Review of contract testing organization protocols and reports • Ensure departmental records are progressed in agreed timelines and provide monthly departmental metrics • Experience within a QC testing laboratory in a GMP regulated environment • Good interpersonal and communication skills • Delivery focused; strong organizational and time management skills • Able to prioritise workload and adapt to changing business needs • Computer literate (Word, Excel, MS Office) The Candidate You will have 4 or more years of experience working in a BioPharm environment. You will have a core understanding of current GMP, with experience in a number of different techniques pertaining to QC Testing. E.g. Elisa, PCR, SDS-Page etc. ----- This is an incredible opportunity to really push your career forwards in a thriving company. For more information and a confidential discussion, contact Kieran Whitaker on: - Tel: 0161 923 8174 Email: Kieran.whittaker@wearenorthpoint.com Salary is negotiable on experience

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  • QC Manager

    Salary: £60000 Location: OXFORD

    My client is a fast growing Biopharmaceutical company based in the Oxford area who are currently looking for an experience QC manager to join their team. The company have expanded from 70 people in 2014 to over 250 in 2017.The organisation is on the cutting edge of gene and cell therapy treatments, and have developed an indutry leading technology leading to contracts of more than £100 million already in 2017. The departments primary focus is based around in-process, QC release and stability testing for a number of my clients large pharma and biopharma based clients. They use a mixtue of chemical and biochemical based testing methodologies including qPCR, HPLC, spectrophotemtry and UV. The ideal candidate for this position should have the following skills; + In excess of 10 years working within the QC environment of a pharma or biopharma organisation. + Strong GMP experience. + Team leading exposure + Departmental management experience of a similar laboratory, + Understanding of method development and validation Ideally candidates will currently be a QC manager within a respected pharma company, however applications will be considered from candidates who are currently working in a senior QC capacity and are looking for the next step. Please bear in mind that if the latter is the case then extensive experience must have been developed previously. Salaries are expected to be in the 45k to 60k region.

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