Jobs

We found 178 job(s) for you:

  • QA Officer

    Salary: £25000 Location: BRADFORD

    The Client My client is a knowledge based, science led business focused on delivering the expertise and capabilities their clients demand. Working in the pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products sectors. They support drug discovery and development in the pharmaceutical and biotechnology markets, by providing 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 The Quality Assurance Officer’s function is the independent Good Laboratory Practice (GLP) monitoring of work conducted on site. As the Bradford site conducts work to Good Manufacturing Practices Regulations (GMP) this role will have the opportunity to cross train in GMP auditing. Responsibilities • Participate in reviewing 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. • Prepare and conduct computer validation audits. • Participate in scheduling and conducting external audits. • Review forms, where required. • 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. • Participate and perform administrative tasks as required. Salary is negotiable on experience ----- Are you prepared to begin a new chapter in your career? If so, this could be the role for you! For more information and a confidential discussion, please contact Kieran Whittaker on: - Tel: - 0161 923 8174 Email: - Kieran.whittaker@wearenorthpoint.com

    View
  • Java Software Engineer

    Salary: £35000 Location: SOUTHAMPTON

    Based in Southampton my client is an award winning, software design company, dealing with cutting edge technology for the aerospace, energy and defence sectors. Due to current growth they are looking for a talented Software Engineer with experience in C# or Java (opportunities available in both) and some industry experience. This is a fantastic company with a diverse culture and a passion for its industry. They are looking for like-minded individuals to help propel the company forward and in return can offer a great working environment, excellent benefits and career development opportunities. You will be responsible for developing software for safety-critical embedded systems, working on all development phases of the V-cycle and Performing verification and validation testing in line with project schedules, processes and standards. You will have: At least 3 years of experience using Java, Spring, Hibernate, MySQL, Maven, Git and Java Application Servers; Knowledgeable with web architectures and services (HTTP, SOA, REST, JSON, etc.); Salary £25-£35,000 dependant on experience Excellent career development options Great beenfits

    View
  • Oncology Consultant

    Salary: £80000 Location: LONDON

    Oncological Consultancy - London - £ flexible My Client are a strategic consultancy firm who are set up to help biotech/pharma companies in their decision making processes. An award winning, multinational consultancy this client has opportunities for growth London, New York, San Fransisco, New Delhi and Beijing. This multinational focus allows the company to deliver effective consultancy to the global market. Due to continued growth, a fantastic opportunity for an oncology consultant has opened up. The role itself has an excellent salary and benefits, and would be perfect for someone with; * A successful career in commercial oncology looking to move into a consultancy role. * PhD in Life Science focusing on immuno-oncology and immunotherapy. * Project Managerment * Data analysis * A strong Conference and publication history. If this sounds like you then feel free to get in touch.

    View
  • Technical Leader

    Salary: £32000 Location: BRADFORD

    My client is a multinational business with laboratories throughout the UK focusing on pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical and chemical sectors. Due to expansion, there is an urgent need for a Technical Lead with experience in analytical sciences. * PhD in related Discipline * Small Molecule and Drug Development experience * Experience with Drug solubility If you are looking for a new position and would like to know more, please do get in touch.

    View
  • Senior Design Engineer -IVD medical devices

    Salary: £50000 Location: MANCHESTER

    The Client My client offers an affordable, real-time PCR system that can serve as the basis for rapid detection, quantification, or drug resistance testing of infectious diseases and pathogens, such as TB or Hepatitis. As they further develop their Point of Care philosophy through product development and refinement, they have an opportunity to reach millions of people who currently have limited access to existing diagnostic technology. Ultimately, their goal is to change lives through rapid access to the benefits of molecular diagnostics. The Role Due to a ramp up of their focus on delivering affordable point of care in vitro molecular diagnostics for addressing global infectious disease challenges, my client are looking to strengthen their product engineering team with the addition of an experienced industrial design engineer to support the HCV and TB IVD consumable plastic/ fluidic device programmes; enhancing their system for future success and global impact. Responsibilities • Mechanical/industrial design, prototyping, design verification and manufacturing transfer and component verification • Acting as the industrial design subject matter expert, working closely with programme managers and outsource industrial design innovation companies, contributing to concept development, design transfer oversight, part verification and whole system validation • Leading design history creation including origination of 3D assembly models, schematics, BOMs, material specifications and verification protocols within an ISO 13485 product design and manufacturing environment • Working closely with cross-functional teams of R&D scientists, electronic and software engineers in product design specification, human factors, user experience and FMEA • Supporting internal Operations and outsourced manufacturing teams in process development, validation and incoming goods QC/ component checking • Support Quality/Regulatory teams with CAPA, out-of-spec/non-confirming product investigations on company mechanical/ consumable parts • Maintain good, clear communication with Managers and Directors. Salary is negotiable on experience ----- Are you prepared to begin a new chapter in your career? If so, this could be the role for you! For more information and a confidential discussion, please contact Kieran Whittaker on: - Tel: - 0161 923 8174 Email: - Kieran.whittaker@wearenorthpoint.com

    View
  • Principal Product Development Scientist

    Salary: £50000 Location: WELWYN GARDEN CITY

    Our client is an award-winning clean technology company that has industrialised the process of recycling waste coffee grounds into advanced biofuels. They are a small, dynamic business with offices in London and a factory in Cambridgeshire. They are passionate about their vision, values and people, and aim to be sustainable in everything they do whilst giving our people the space to grow and develop in a fast-moving and high-growth environment. They are looking for hard working self-starters to join the team, who can keep up with the pace and want to make a difference. They still work in relatively small teams, so there’s no room for coasting along. They are friendly, happy, and most importantly, we work hard. We’re not afraid to get our hands dirty and we’re all hugely passionate about what bio-bean is trying to achieve. The companies head office is in London, with their scientific laboratory is in the BioPark at Welwyn Garden City moving to new premises in Cambridgeshire in the near future. + Previous experience of at least 7 years in industry bringing new innovative, (bio-)chemical compound products to market within the flavour & fragrance, food & beverage or other relevant industry sector, with experience of formulation equipment and processing + A Masters or PhD in Chemistry, food science or a related, relevant discipline + Excellent verbal communication skills, with the ability to communicate clearly, effectively and appropriately with colleagues at all levels. + Excellence in technical report writing plus the ability to bring both detailed information and technical data to commercial life for a range of different audiences. + Experience of presenting to large audiences and networking at relevant external events. + Ability to track and manage an opex and capex budget + Experience of developing, coaching and leading other scientists and work colleagues Salaries are expected to be in the 50k range.

    View
  • Process Compliance Officer

    Salary: £40000 Location: OXFORD

    Our client is a leading biopharmaceuticals organisation based from state-of-the-art offices in Oxford. Having rapidly expanded over the course of the last 3 years to over 300 employees, they are currently recruiting a wide range of biotechnology based positions. The company are at the forefront of the gene and cell therapy sector, having built a novel drug development platform which they leverage to develop products both in-house and with partners. Their proprietary portfolio of products include a lead product for Parkinson’s disease. With preparations completed for this to move into the clinic, they are in active discussions with a number of third parties to potentially out-licence the product, thereby sharing the costs and the risks whilst retaining an interest in the value of the product as it progresses. Other products at development stage include a gene-based therapies for corneal graft rejection and cancer. The company have a very respected name in the industry, and offer potential candidates a strong career path, generous financial renumeration, and a caring yet focussed environment in which to flourish. We are helping them to recruit a process compliance officer within their manufgacturing division. Candidates should have the following skills and experiences; • Experience of working within a GMP manufacturing environment • Experience with Manufacturing documentation such as SOPs, Deviations, Change Controls Risk Assessments and CAPAs • Competency in Microsoft Office • Familiarity with Root Cause Analysis techniques and the ability to amalgamate and interpret complex data in an investigative capacity would be an advantage Salaries are expected to be around the 40k mark.

    View
  • Quality Systems Officer

    Salary: £35000 Location: OXFORD

    Our client is a leading biopharmaceuticals organisation based from state-of-the-art offices in Oxford. Having rapidly expanded over the course of the last 3 years to over 300 employees, they are currently recruiting a wide range of biotechnology based positions. The company are at the forefront of the gene and cell therapy sector, having built a novel drug development platform which they leverage to develop products both in-house and with partners. Their proprietary portfolio of products include a lead product for Parkinson’s disease. With preparations completed for this to move into the clinic, they are in active discussions with a number of third parties to potentially out-licence the product, thereby sharing the costs and the risks whilst retaining an interest in the value of the product as it progresses. Other products at development stage include a gene-based therapies for corneal graft rejection and cancer. The company have a very respected name in the industry, and offer potential candidates a strong career path, generous financial renumeration, and a caring yet focussed environment in which to flourish. We are helping them to recruit an experienced Quality Systems Officer for their quality department. Candidate should have the following skills and experience; + Minimum of 3 years working within a GMP pharmeuticals environment. + Solid working knowledge of validation and quality management systems. + Experience conducting quality based audits, investigations and root cause analysis. + Experience of document control and/or records management. + Strong team skills Salaries for the role are expected to be around the 35k mark.

    View
  • Senior Downstream Processing Scientist

    Salary: £45000 Location: OXFORD

    Our client is a leading biopharmaceuticals organisation based from state-of-the-art offices in Oxford. Having rapidly expanded over the course of the last 3 years to over 300 employees, they are currently recruiting a wide range of biotechnology based positions. The company are at the forefront of the gene and cell therapy sector, having built a novel drug development platform which they leverage to develop products both in-house and with partners. Their proprietary portfolio of products include a lead product for Parkinson’s disease. With preparations completed for this to move into the clinic, they are in active discussions with a number of third parties to potentially out-licence the product, thereby sharing the costs and the risks whilst retaining an interest in the value of the product as it progresses. Other products at development stage include a gene-based therapies for corneal graft rejection and cancer. The company have a very respected name in the industry, and offer potential candidates a strong career path, generous financial renumeration, and a caring yet focussed environment in which to flourish. We are currently helping them to recruit a senior downstream scientist within their process, research and development team. Candidates will be recognized experts in downstream processing including bioprocess design, protein expression and purification. They will be primarily involved in purifying and characterizing a variety of therapeutic candidates in support of projects from early stage research to pre-clinical programs. Process, Research and Development works with the companies research teams involved in vector and cell engineering to ensure the seamless transfer of processes from research to manufacturing. The scope of work may include, but are not limited to vector purification, novel purifications, purification process development and verification, technology assessment, data analysis and project reporting. The individual must have a demonstrated ability to work independently and to manage multiple projects either through direct supervision or in collaboration with the programme team. The individual must be innovative and creative, show initiative, collaborative ability and have good general science management skills. Applicants are expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. The individual should also enjoy working in a team setting and be able to work well with both research scientists and as well as external collaborators. Salaries for the senior downstream processing roles are expected to be in the 40 to 45k range.

    View
  • Analytical Scientist (PR&D)

    Salary: £0 Location: OXFORD

    Our client is a leading biopharmaceuticals organisation based from state-of-the-art offices in Oxford. Having rapidly expanded over the course of the last 3 years to over 300 employees, they are currently recruiting a wide range of biotechnology based positions. The company are at the forefront of the gene and cell therapy sector, having built a novel drug development platform which they leverage to develop products both in-house and with partners. Their proprietary portfolio of products include a lead product for Parkinson’s disease. With preparations completed for this to move into the clinic, they are in active discussions with a number of third parties to potentially out-licence the product, thereby sharing the costs and the risks whilst retaining an interest in the value of the product as it progresses. Other products at development stage include a gene-based therapies for corneal graft rejection and cancer. The company have a very respected name in the industry, and offer potential candidates a strong career path, generous financial renumeration, and a caring yet focussed environment in which to flourish. We are helping them to recruit an analytical scientist within their process, research and development team. Candidates should have the following skills and experiences; •An undergraduate degree (or equivalent-level qualification) in a Life Sciences or Biotechnology-related subject •Good aseptic techniques •Knowledge of general cellular and molecular biology laboratory techniques •Practical experience of a range of bioprocess analytical techniques (such as cell-based assays, FACS based assays, nucleic acid extractions, qPCR, SDS PAGE, Western blot analysis, ELISA, HPLC, etc.) •The ability to work in a high paced team environment and to, meet challenging deadlines •Demonstrated ability to work independently as well as in a team setting •Strong written and verbal skills Salaries are expected to be in the 35-38k range.

    View

« previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 next »