Pharmaceuticals

  • Research Scientist- (Discovery II Host Team) 11/20/2018 12:00:00 AM

    Salary: £0 Location: Aberdeen

    I am currently working with a leading pharmaceutical company who are pioneering a new class of revolutionary biotherapeutic medicines. Due to continued success and a robust product pipeline they are now recruiting for a number of positions. This role will primarily provide scientific expertise to the activities of the Discovery II Host team. The primary focus of the team is to investigate the mechanisms behind the host-microbe interactions of their preclinical LBP candidates. Proficiency in running a variety of cellular and molecular techniques is required along with independent and flexible working. The post-holder will also be responsible for writing reports and SOPs, contributing to writing papers, present at internal and external meetings. If you have a strong immunological background and a want to work with a company who are truly revolutionising the way in which we treat some of the world’s most tenacious diseases, then this could be the opportunity for you. For more information please contact Kieran Whittaker for a confidential discussion on: Email: Kieran.whittaker@wearenorthpoint.com Phone: 0161 923 8174

    View
  • Research Scientist (Microbiology) 11/20/2018 12:00:00 AM

    Salary: £0 Location: Aberdeen

    I am currently working with a leading pharmaceutical company who are pioneering a new class of revolutionary biotherapeutic medicines. Due to continued success and a robust product pipeline they are now recruiting for a number of positions. This role will primarily perform testing required to support the core research and development program of the Discovery I Micro team. The primary focus of the Discovery 1 Micro team is to carry out high-throughput and secondary screening of the propriety strain library to identify candidate LBPs capable of modulating host-microbe interactions. The Research Scientist is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfils generally accepted professional/industry standards. The Research scientist will be expected to propose new screening strategies and introduce and validate new screening approaches/methods ensuring they are current and compliant with industry standards and regulations. Requirements also include maintaining a thorough understanding of my client’s services, technical principles and applications. Proficiency in running a variety of assays and molecular techniques are required along with independent and flexible working. The post holder will also be responsible for writing reports and SOPs, contributing to writing papers and present findings at internal and external meetings. If you have a strong microbiological background, experience working with human bacteria, anaerobic cells and a want to work with a company who are truly revolutionising the way in which we treat some of the world’s most tenacious diseases, then this could be the opportunity for you. For more information please contact Kieran Whittaker for a confidential discussion on: Email: Kieran.whittaker@wearenorthpoint.com Phone: 0161 923 8174

    View
  • Finance Manager 11/19/2018 12:00:00 AM

    Salary: £0 Location: Stevenage

    I am currently looking for a Finance Manager ready to take on a new challenge with our client, based in Stevenage, UK. As a result of continued development, my client is now looking for a hands-on Finance Manager to join their team with responsibility over a number of the finance processes and wider finance function. Reporting to the Financial Controller, the ideal candidate will be in a position to embrace the challenges faced by a developing company whilst aspiring to ensure that processes and controls are adhered to. If you are considering a move; I’d love to hear from you! This is an urgent appointment and the closing date is the 23rd of November, so please dont hesitate to contact me should you have an interest. For a confidential discussion please contact me on: - Tel: 0161 923 8174 Email: kieran.whittaker@wearenorthpoint.co.uk

    View
  • QC Micro Technologist 11/9/2018 12:00:00 AM

    Salary: £0 Location: Salisbury

    My client is a fast-growing biopharmaceuticals company, specialising in the manufacturing and development of life-saving biopharmaceutical therapeutics and vaccines. Due to their rapid success, they are looking to hire a talented QC Technologist to join the bacteriology department. The Bacteriology Technical Services Group is a Unit of the Quality Control (QC) Biological Services which undertake and perform microbiological QC analyses in support of my clients licensed production, service, validation and developmental programmes. Key responsibilities: + To carry out all work in compliance with cGMP + To test microbiological samples from all stages of the production processes of licensed and developmental products and to assess the results against pre-set standards and specifications + To undertake identification of micro-organisms isolated from microbiological tests and samples + To record all information and data clearly and accurately + To pre-test media used within QC and Production against pre-set specifications + To maintain the Bacteriology Technical Services Culture Collection, media stocks, and necessary consumables to ensure the efficient running of the group ***What the Quality Technician will get*** • A Competitive Basic Salary • Full training and investment • Pension scheme • 30 days’ holiday • Free onsite parking • A Canteen, gym and active sports & social club

    View
  • Computer System Validation Specialist 11/8/2018 12:00:00 AM

    Salary: £42000 Location: Salisbury

    My client is a fast-growing biopharmaceuticals company, specialising in the manufacturing and development of life-saving biopharmaceutical therapeutics. Due to their rapid success, they are looking to hire a permanent Computer Systems Validation Specialist The ideal candidate will have validation experience within the Pharmaceutical Industry and have previously worked within a GLP or GMP environment. Knowledge of CAPA, Discrepancies and Non-Conformance Management would be an advantage. Established use of Microsoft Word and Excel is essential. ***What the Computer Systems Validation Specialist will do*** + Take the lead in computer system validation and compliance, manage and deliver specific Validation Projects according to the business priorities + Continuous improvement of validation systems and procedures + Create validation documentation including protocols and reports & manage the timely closure of any discrepancies or non-conformities + Maintaining the ongoing compliance of computer systems associated with equipment + Undertake all work in accordance with GxP ***What the Computer Systems Validation Specialist will get*** • A Competitive Basic Salary of up to £42,000 • Full training and investment • Pension scheme • 30 days’ holiday • Free onsite parking • A Canteen, gym and active sports & social club

    View
  • Research Associate / Research Scientist - Discovery Pharmacology 10/29/2018 12:00:00 AM

    Salary: £0 Location: Cambridge

    My client is a rapidly expanding bio-pharmaceutical company developing a novel class of medicines to treat cancers and other important diseases based on its proprietary product platform. Headquartered in Cambridge, U.K., with U.S. operations in Boston, Massachusetts. As their team in the UK expands, they now have an exciting new opportunity for a skilled and motivated Research Associate or Research Scientist to join their Discovery Pharmacology Team. You will enjoy a varied and rewarding role, developing and running a range of in vitro assays to screen and characterise novel peptides identified by the platform. You will be joining an established and expanding biology team, working across a variety of disease areas supporting both internal oncology and partnered programs, serving multiple therapeutic areas. If you are ready to take the next step in your career or just want a confidential discussion about your options, please dont hesitate to contact Kieran Whittaker on 0161 923 8174 or kieran.whittaker@wearenorthpoint.com

    View
  • Process Engineer 10/16/2018 12:00:00 AM

    Salary: £0 Location: Salisbury

    My Client is a leading manufacturer of biopharmaceutical products and with a rich history of pharmaceutical development in vaccines and therapeutics they are looking for an outstanding process engineer to join their team. The Process Engineer is the System technical expert for all Engineering Utilities systems within the GMP Envelope, and is responsible for the identification of and managing small projects relating to the utilities systems and interfacing with the wider Pharmaceutical Engineering group to ensure Utilities systems within the GMP envelope remain compliant with current Good Manufacturing Practice. Roles and Responsibilities To monitor Utilities equipment trend data as provided by the computerised maintenance management system and liaison with the maintenance teams/users, to recommend and manage process improvements/initiatives and when required prepare justifications for submission within the appropriate capital budget. ? Project Manage small business critical GMP projects as delegated by the Process Engineering Manager in accordance with the GMP Capital Project procedure. ? Represent the Engineering function at BSI, MHRA and FDA audits as subject matter expert for Utilities supported by the Process Engineering Manager. ? To be responsible for the writing, and review of User Requirement specifications, SOP’s, and generation of design documentation related to Utilities systems and other equipment within the GMP envelope. ? Review and Approval of Engineering technical regulatory documents as required to support the Engineering function including review and approval of Safety related documents such as pressure systems written schemes of examination. For more information please contact Robert Frame on: 0161 504 8058 or robert.frame@wearenorthpoint.com

    View
  • Quality Manager GLP IDDS 10/2/2018 12:00:00 AM

    Salary: £35000 Location: Dundee

    My client is a knowledge based, science led business focused on delivering the expertise and capabilities their clients demand. We work in the pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products sectors. My client supports drug discovery and development in the pharmaceutical and biotechnology markets. The site in particular provides testing and specialist analytical services and consultancy to the food and environmental sectors. They also provide toxicology services to the agrochemical, consumer products, chemical and pharmaceutical industries and materials chemistry services to the petrochemical industry. The Role An opportunity has arisen to join the team in Dundee as Quality Manager. Due to substantial business growth my client has recently expanded their Regulatory Good Laboratory Practice (GLP) services at the Dundee site. To do this the Quality Manager shall: Assume responsibility for the maintenance of the quality assurance programme in accordance with current regulations and guidance. Assume responsibility for the day to day management of QA functions. Perform GLP and GCP monitoring of work conducted. Review the Quality Assurance programme to ensure it meets regulatory requirements and is of maximum benefit reporting any deficiencies to the Group Head of Quality Assurance. Develop or improve in conjunction with the Group Head of Quality Assurance auditing strategies for new systems introduced at Dundee or other sites as required. Develop in conjunction with the Group Head of Quality Assurance and deliver formal GLP and GCP training. Act as QA contact for site.

    View
  • Deputy Quality Manager - Analytical Services 10/1/2018 12:00:00 AM

    Salary: £35000 Location: Manchester

    My client is a knowledge based, science led business focused on delivering the expertise and capabilities their clients demand. They have a broad scope and focus their work in the pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products sectors. My client works in supporting drug discovery and development in the pharmaceutical and biotechnology markets. The Role The role of the Deputy Quality Manager is to work with the Quality Manager to manage and maintain the day to day running and compliance of the Quality Management Systems within the Environmental Testing Laboratories in Manchester. The Laboratories are currently accredited to the ISO 17025 Standard by UKAS. Main Duties to: Work with the Quality Team in implementing and maintaining the quality systems and processes within the Laboratories. Maintain the site audit schedule reporting any deficiencies to the Quality Manager. Perform and review audits of systems, processes and records. Assist with audits by customers and regulators/accreditation bodies. Assist with reviewing quality control charts, proficiency testing scheme results and appropriate follow ups as required. Assist with the control, issue and maintenance of documents within the quality system. When required, working with Quality Managers in monitoring of customer complaints and items of non-conforming work. Modify quality system documentation and Laboratory Standard Operating Procedures (SOPs) under supervision of the Quality Manager. Qualifications/Role Requirements: A science graduate with experience in ISO17025 testing industry. Experience in a high throughput environment would be an advantage. Thorough knowledge, skills and abilities in managing ISO 17025 guidance. Proven knowledge and experience of scheduling and performing audits. Experience in hosting/supporting customer accreditation inspections. Excellent organisational, interpersonal and communication skills. Competent at preparing and delivering presentations to employees, customers and regulatory bodies. Ability to challenge and drive quality and a compliant culture forward. Experience in developing audit schedules and training initiatives.

    View
  • Quality Assurance Officer GLP Analytical Services 10/1/2018 12:00:00 AM

    Salary: £30000 Location: Dundee

    My client is a knowledge based, science led business focused on delivering the expertise and capabilities their clients demand. We work in the pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products sectors. My client supports drug discovery and development in the pharmaceutical and biotechnology markets. The site in particular provides testing and specialist analytical services and consultancy to the food and environmental sectors. They also provide toxicology services to the agrochemical, consumer products, chemical and pharmaceutical industries and materials chemistry services to the petrochemical industry. The Role Due to sustained business growth, the Dundee site has a brand new opportunity to join the site as a Quality Assurance Officer. The Quality Assurance Officer’s function is the independent Good Laboratory Practice (GLP) monitoring of work conducted at the Dundee site as required by the regulatory guidelines employed therein. Main Duties: Review Study Plans where required. Schedule and conduct all audits as assigned. Write up findings of Quality Assurance Audits and Inspections. Report all audit findings to management and Study Director/Principal Investigator (as applicable). Prepare and issue Quality Assurance Statements. Write and review Quality Assurance Standard Operating Procedures. Review Standard Operating Procedures for compliance with principles of GLP, as required. Conduct computer validation audits. Schedule and conduct external audits. Conduct reviews of forms. Train other personnel in all aspects of Quality Assurance Systems and Procedures as required. Advise management of any deficiencies in Regulatory Requirements. Host or partake in Sponsor and Regulatory visits as appropriate. Liaise with site personnel to ensure a full understanding of regulatory requirements.

    View

« previous 1 2 3 4 5 next »