http://www.midianls.co.ukLatest Midian JobsWed, 10 Mar 2010 18:35:44 +0000en-ushttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582467http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582467Fri, 26 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Symbol font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br b Our client, a leading Virology Research Company in central London have an opportunity for a QA Manager GCP br br b RESPONSIBILITIES br b Reporting to the Quality Director, your responsibilities will include, but not be limited to br span span class ts2 nbsp nbsp nbsp span span class ts1 Implement and manage the Quality System in line with Business strategy. br span span class ts2 nbsp nbsp nbsp span span class ts1 Develop the QA GCP audit strategy and implement the audit programme in line with the overall QA strategy. br span span class ts2 nbsp nbsp nbsp span span class ts1 Assure management of the compliance level of clinical trials in accordance with business and statutory regulations. br span span class ts2 nbsp nbsp nbsp span span class ts1 Report critical GCP non-compliance to Quality Director and collaborate with Clients during Client audits br span span class ts2 nbsp nbsp nbsp span span class ts1 Delivering the GCP audit programme to verify compliance with GCP, and determine the effectiveness of the Company s quality systems and procedures within agreed timescales br span span class ts2 nbsp nbsp nbsp span span class ts1 Delivering the SOP Management System br span span class ts2 nbsp nbsp nbsp span span class ts1 Acting for the Quality Director in their absence by hosting regulatory inspections and client audits covering GCP and Quality systems. br br b EDUCATION amp EXPERIENCE br b br The Successful candidate will have br span span class ts2 nbsp nbsp nbsp span span class ts1 Minimum education to degree level, and ideally a qualification in quality or QA. br span span class ts2 nbsp nbsp nbsp span span class ts1 Minimum of 5-8 years QA and proven auditing experience across full range of clinical audit types including CROs, Investigator sites, protocols, clinical study reports, systems and submissions. br span span class ts2 nbsp nbsp nbsp span span class ts1 Proven management experience, minimum of 2-3 years. br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience in supporting regulatory inspections and client audits. Hosting inspections including follow up and close-out an advantage. br span span class ts2 nbsp nbsp nbsp span span class ts1 Good knowledge of phase I - IV studies, bioanalytical, PK, skin, blood and urine laboratory analysis. Experience auditing all these study types an advantage. br span span class ts2 nbsp nbsp nbsp span span class ts1 Hands on adaptable pragmatic approach br span span class ts2 nbsp nbsp nbsp span span class ts1 Excellent attention to detail br span span class ts2 nbsp nbsp nbsp span span class ts1 Innovative br span span class ts2 nbsp nbsp nbsp span span class ts1 Excellent multitasking capabilities br br span span class ts1 span body html LONDONLocation: LONDONhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582191http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582191Mon, 15 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br b Our client, an innovative stem cell biology company, are currently seeking a b Stem Cell Culture Scientist, b to join them on a permanent basis. nbsp The main role of the post will be the maintenance and culture of Human Stem Cell lines and their subsequent analysis. br br b RESPONSIBILITIES br b The Stem Cell Culture Scientist will undertake the culture and maintenance of human stem cell lines, in various research projects, and their subsequent analysis, using a variety of assays. In addition they will be responsible for the day to day running of the stem cell culture facility. The post holder would be expected to maintain a high level of data recording for the various projects. br br br b EDUCATION amp EXPERIENCE br b The applicant will have a minimum of a degree or equivalent qualification , in the life sciences. Experience in the tissue culture of human cells is required, specifically stem cells, and a working knowledge of stem cell analysis assays would be beneficial, but not essential. br They should also possess good communication skills and be able to produce high quality documentation and reports for internal meetings, clients and customers. br br br span div align justify span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582405http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582405Mon, 15 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 span.ts3 font-family Times New Roman font-size 10pt color 000000 span.ts4 font-family Times New Roman font-size 12pt color 000000 span.ts5 font-family Arial font-size 12pt color 000000 span.ts6 font-family Arial font-size 9pt color 000000 -- style head body div align justify b span class ts1 SUMMARY br b Our client, a global Biotech firm in Central Scotland, who offers contract services and nbsp manufactures products for the bioscience industry, have a new opportunity for a b Validation Officer b in their Quality Department. br br span div div align justify b span class ts2 In return you will receive a highly competitive salary and benefits package including bonus and pension scheme. br span b br br div div align justify b span class ts1 RESPONSIBILITIES br b div The key role of the Validation Officer is to lead multi-discipline validation teams to prepare validation protocols and reports in accordance with operational requirements, ensuring they comply with statutory regulatory requirements and the principals of Good Manufacturing Practice. br br span div align justify b span class ts1 EDUCATION amp EXPERIENCE b br br span div span class ts1 Relevant Degree and at least 2 years industrial experience in producing validation protocols, reports and associated documentation in line with the principals of Good Manufacturing Practice. br br span span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582002http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582002Tue, 19 Jan 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Symbol font-size 10pt color 000000 -- style head body div align justify b span class ts1 SUMMARY br b br div div align justify Applicants are invited to apply for the role of b PERMANENT Protein Scientist b Bioconjugation Group . As a highly experienced Development Scientist you will lead a small team of protein scientists in aspects of project delivery involved in developing robust scaleable processes for the conjugation of cytotoxic drug to antibodies, proteins and peptides as parenteral biologic drugs for the oncology sector. br br The successful candidate will be nbsp working with a leading global supplier of complex organic molecules. nbsp Due to its success our client has several new projects pushing them into an exciting phase of rapid expansion. br br b RESPONSIBILITIES br br b As an experienced Protein Scientist, you will take on each development project as a complete package of development and analysis. The responsibilities will include, but not be limited to br span div span class ts2 nbsp nbsp nbsp span span class ts1 Lead, plan and undertake development and technology transfer projects in line with agreed objectives and timelines br span span class ts2 nbsp nbsp nbsp span span class ts1 Provide technical support and advice for commissioning and manufacturing activities relating to processes developed or transferred. br span span class ts2 nbsp nbsp nbsp span span class ts1 Communicate with other technical personnel in R amp D, QC, QA and manufacturing to exchange information and results that are required to make milestone decisions in development and siting work. br span span class ts2 nbsp nbsp nbsp span span class ts1 Daily task management, training and mentoring of Experiment Scientists, provide performance data to line manager for appraisals. br span span class ts2 nbsp nbsp nbsp span span class ts1 Housekeeping - ensures the development laboratory and other associated areas are kept in a compliant manner and actions any housekeeping requirements accordingly. br span span class ts2 nbsp nbsp nbsp span span class ts1 Will plan development work programmes and manage delivery according to project timelines. br span span class ts2 nbsp nbsp nbsp span span class ts1 Synthesis of protein conjugates in R amp D environment br span span class ts2 nbsp nbsp nbsp span span class ts1 Use of appropriate analytical techniques for characterization br span span class ts2 nbsp nbsp nbsp span span class ts1 Process amp scale-up activities br br div align justify b EDUCATION amp EXPERIENCE br br b div div align justify Ideally you will have protein development characterisation experience and should be comfortable with lab scale protein handling and analysis. This must be coupled with large-scale bio-processing and or protein manufacturing experience. The ideal candidate must be an excellent communicator and will need to demonstrate expertise in one or more of the following br span div span class ts2 nbsp nbsp nbsp span span class ts1 Bioconjugation process development br span span class ts2 nbsp nbsp nbsp span span class ts1 Downstream processing of protein based biologics br span span class ts2 nbsp nbsp nbsp span span class ts1 The use of DoE approach in process development, optimization and characterisation br span span class ts2 nbsp nbsp nbsp span span class ts1 Formulation development for protein based parenteral drugs br span span class ts2 nbsp nbsp nbsp span span class ts1 Scale up and transfer of development projects into a GMP environment br br div align justify The ideal candidate will have as a minimum br span div div align justify span class ts2 nbsp nbsp nbsp span span class ts1 A degree in a relevant scientific discipline br span span class ts2 nbsp nbsp nbsp span span class ts1 At least 2 years experience in process development in a regulated environment br span span class ts2 nbsp nbsp nbsp span span class ts1 A sound understanding of GMP br br span div span class ts1 span body html GrangemouthLocation: Grangemouthhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580587http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580587Mon, 9 Nov 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580526http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580526Mon, 9 Nov 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582003http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582003Wed, 10 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Calibri font-size 10pt color 000000 span.ts2 font-family Calibri font-size 11pt color 000000 span.ts3 font-family Arial font-size 11pt color 000000 span.ts4 font-family Arial font-size 10pt color 000000 span.ts5 font-family Symbol font-size 10pt color 000000 -- style head body div align justify b span class ts2 Summary b br span span class ts4 Our client, b a biotechnology company with a reputed global reputation b specialises in all aspects of rapid test technology. Due to continued expansion they have an exciting opportunity for a b Development Scientist b to be responsible for the development amp manufacture of products. br br b In return our client offers a challenging career in an expanding dynamic company with excellent salary and benefits package and opportunities for career development. br b br br span b span class ts2 Responsibilities br b span div div align justify span class ts4 The role will be split across 2 departments, manufacturing and R amp D, the successful candidate will be involved in assay development and will work as part of a small dynamic team of scientists. br br span div div align justify b span class ts2 Education amp Experience b br span div span class ts4 Essential br span span class ts5 nbsp nbsp nbsp span span class ts4 Good BSc in Biochemistry, Biotechnology or related subject br span span class ts5 nbsp nbsp nbsp span span class ts4 Experience of assay development br span span class ts5 nbsp nbsp nbsp span span class ts4 Enthusiastic and dynamic individual br span span class ts5 nbsp nbsp nbsp span span class ts4 Team orientated with flexible approach to work br span span class ts5 nbsp nbsp nbsp span span class ts4 Experience of GLP or GMP br br Desirable br span span class ts5 nbsp nbsp nbsp span span class ts4 Experience of lateral flow technology br br span span class ts1 span body html DundeeLocation: Dundeehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581088http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581088Mon, 7 Dec 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582417http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582417Tue, 2 Mar 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582524http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582524Mon, 8 Mar 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 span.ts3 font-family Symbol font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br b br Our client, an innovative pharmaceutical company, are currently recruiting for a b Clinical QA Manager. nbsp b This is a span span class ts2 n excellent opportunity to work in one of the most exciting areas of modern medicine as the client is at a key point in its development with Phase III oncology studies due to start in the US, Europe and other territories. br br span b span class ts1 RESPONSIBILITIES br b br span span class ts2 As Clinical QA Manager you will manage the GCP CQA group concentrating on these Phase III studies leading to US FDA NDA approval. nbsp As a key manager within the multi-disciplined company QA team you will utilise your extensive GCP knowledge and excellent leadership and communication skills to lead the CQA audit team and oversee the design and implementation of the audit programme for the clinical development function, including internal systems, external suppliers, documentation and international investigator site audits. nbsp You will also provide support, advice, education and training to other departments involved in clinical trials and may become involved with cross-functional GMP and GLP audits. nbsp As part of the role, you will be tasked with organising a quality system for introducing assessments for training competency at all operational levels. br As well as having knowledge of clinical trials safety reporting requirements, you will also have experience of the commercial commitments for Pharmacovigilance for both EU and US, in order to manage quality audits for these systems in Phase IV studies and a worldwide marketplace. br br You will host Regulatory Authority GCP and Pharmacovigilance inspections where required and manage the CAPA process to close out. nbsp You will give strong input into the set up and maintenance of procedures within Clinical Development departments and support the development and audit of licence application dossiers. This will be a broad based position, providing exposure to all aspects of drug development. Reporting to the Director of Quality and based at the company s Clinical Development offices in Cambridgeshire, this is a highly interactive and influential role, requiring self-reliance, effective strategic thinking and planning skills, the ability to network, lead a busy but well-established and confident team, and build successful interfaces both internally and externally. nbsp Excellent leadership, negotiation and influencing skills are absolutely essential. br br br span b span class ts1 EDUCATION amp EXPERIENCE br b br span span class ts3 nbsp nbsp nbsp span span class ts1 Ideally a bioscience degree br span span class ts3 nbsp nbsp nbsp span span class ts1 Broad experience in clinical research and commercial pharmacovigilance br span span class ts3 nbsp nbsp nbsp span span class ts1 Must have worked in a GCP or regulatory environment for at least eight years br span span class ts3 nbsp nbsp nbsp span span class ts1 Three to five years quality assurance experience in a GXP environment br span span class ts3 nbsp nbsp nbsp span span class ts1 A working knowledge of Oncology or Neuroscience would be advantageous br span span class ts3 nbsp nbsp nbsp span span class ts1 Experience of successfully managing a team br span span class ts3 nbsp nbsp nbsp span span class ts1 A full driving licence is required along with the ability to travel approximately 25 both within the UK and overseas br br br span span class ts1 span body html South EastLocation: South Easthttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582468http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582468Thu, 4 Mar 2010 +0000Excellent Negotiable PackageEdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582525http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582525Tue, 9 Mar 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br b br Our client, a world leading pharmaceutical company, seeks to appoint a Trade Manager-North East, Midlands, East Anglia of England br br This is a unique and challenging opportunity to join one of the world s leading pharmaceutical companies. The opportunities to grow and develop as the company expands are effectively without limit and the remuneration and bonus packages will not be a barrier to the right candidate. br br b RESPONSIBILITIES br b br The Trade Manager will promote and sell a range of animal healthcare products to the animal health trade, key accounts and animal health outlets. br br br b EDUCATION amp EXPERIENCE br b br The requirement is for a high calibre individual with a demonstrable track record of achievement in delivery of top line sales targets in a competitive business to business environment. The ideal candidate will already have b previous experience at a senior level in a sales role in the animal health sector b . Self sufficient, self motivated and willing to travel extensively to fulfil the needs of this role, the ideal candidate will have a b life sciences background b with skills and knowledge gained from significant commercial experience, as well as a successful track record in field sales. br br br span span class ts1 span body html Location: http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582193http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582193Tue, 16 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Times New Roman font-size 10pt color 000000 span.ts3 font-family Times New Roman font-size 9pt color 000000 span.ts4 font-family Arial font-size 9pt color 000000 span.ts5 font-family Symbol font-size 10pt color 000000 -- style head body div align justify b span class ts1 SUMMARY br b br span div div align justify span class ts1 Our client, a specialist provider of ADME and pharmacokinetic screening services, are currently recruiting for a Senior Research Scientist. nbsp Working within a small team the successful candidate will be responsible for all assay validation work in the group ensuring that all work is performed by trained individuals and to a high standard. br br br span div div align justify b span class ts1 RESPONSIBILITIES br b div div align justify The Senior Research Scientist will work closely with the Laboratory Supervisor of the group in addition to the laboratory assistants and scientists. The individual will ensure that the experimental and data processing aspects of the projects are performed to a high standard and within scheduled time frames. nbsp nbsp Responsibilities will include, but not be limited to br span div div align justify span class ts5 nbsp nbsp nbsp span span class ts1 To act as the single point of contact for all assay validation work in the group and either perform, or provide scientific support guidance to the individuals within the group performing validation of new assays. br span span class ts5 nbsp nbsp nbsp span span class ts1 To be responsible for the design and conduct of non-standard bespoke work within the group following client requests and provide support training for the group. br span span class ts5 nbsp nbsp nbsp span span class ts1 To keep up to date with scientific advances, developments and regulatory guidelines in the area of interest and to inform the group and company of relevant developments. In addition to provide scientific support to the group or Project Managers where appropriate. br span span class ts5 nbsp nbsp nbsp span span class ts1 To be responsible for driving the group forward scientifically, promoting and developing scientific knowledge in the group and presenting data generated internally. br span span class ts5 nbsp nbsp nbsp span span class ts1 To train other individuals within the group in the processes, techniques and interpretation of non-standard work where necessary. br span span class ts5 nbsp nbsp nbsp span span class ts1 To work closely with the Laboratory Supervisor s to schedule staff time for assistance in meeting assay validation targets. In addition to provide support for the routine running of the group when the Laboratory Supervisor is absent. br span span class ts5 nbsp nbsp nbsp span span class ts1 To liaise with the Scientific Computing Group and Information Systems team to enable work to be performed in a timely manner and to improve internal systems processes procedures within the group and company. br br br span div div align justify b span class ts1 EDUCATION amp EXPERIENCE br b br span div span class ts5 nbsp nbsp nbsp span span class ts1 Minimum BSc preferably PhD or equivalent experience in a relevant bio-scientific discipline. br span span class ts5 nbsp nbsp nbsp span span class ts1 Experience minimum ca 4 years in and excellent knowledge of in vitro physicochemical assays and demonstrating a detailed scientific understanding of the following in vitro assays br o Lipophilicity Assays LogD, CHI br o pKa LogP Measurements br o High Throughput Equilibrium Protein Binding br o Solubility Assays br span span class ts5 nbsp nbsp nbsp span span class ts1 Demonstrated experience of assay development and experimental design. br span span class ts5 nbsp nbsp nbsp span span class ts1 Demonstrated use of initiative and innovation to solve problems and troubleshoot whilst working under pressure to deadlines. br span span class ts5 nbsp nbsp nbsp span span class ts1 Able to communicate effectively within a team environment to individuals with varying levels of knowledge and experience. br span span class ts5 nbsp nbsp nbsp span span class ts1 Demonstrated use and understanding of laboratory information management systems and preferably an understanding of LC-MS MS. br span span class ts5 nbsp nbsp nbsp span span class ts1 Knowledge and understanding of PK studies and bioanalysis would be advantageous br span span class ts5 nbsp nbsp nbsp span span class ts1 Experience working in a contract research organisation would be desirable but is not essential. br br span span class ts1 span body html CHESHIRELocation: CHESHIREhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580505http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580505Mon, 19 Jan 2009 +0000On ApplicationScotlandLocation: Scotlandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580506http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580506Thu, 5 Feb 2009 +0000On ApplicationScotlandLocation: Scotlandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580530http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580530Thu, 30 Apr 2009 +0000On ApplicationCambridgeshireLocation: Cambridgeshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581524http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581524Fri, 19 Jun 2009 +0000On ApplicationSouth EastLocation: South Easthttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580829http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580829Tue, 6 Oct 2009 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Symbol font-size 10pt color 000000 span.ts3 font-family Arial font-size 10pt color 000000 span.ts4 font-family Symbol font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br br b Our client, world class, contract biomanufacturing company offering process development services and pre-GMP and cGMP manufacturing, have an opportunity a Development Scientist, due to an exciting period of expansion. br br The post will initially be a 6 month contract with the possibility of extension permanent offer. br br b RESPONSIBILITIES br br b The Development Scientist will be responsible for ensuring the contract manufacture of products to GMP standards by assisting in the technical transfer of projects between Development and Production. br br Your responsibilities will include, but not be limited to br span span class ts2 nbsp nbsp nbsp span span class ts1 Perform activities related to the contract manufacture of Investigational Medicinal Products. br span span class ts2 nbsp nbsp nbsp span span class ts1 Monitor the plant and equipment to ensure continued calibration and maintenance. br span span class ts2 nbsp nbsp nbsp span span class ts1 Analyse, interpret and report experimental data and deviations from expectation to line manager, project team and Quality Assurance in a timely manner. br span span class ts2 nbsp nbsp nbsp span span class ts1 Liaise closely with Senior Scientists and Director of Operations for the effective planning and technical transfer of projects from Development to Engineering and GMP manufacturing according to project plans. br span span class ts2 nbsp nbsp nbsp span span class ts1 Perform work under periodic line management direction according to documented procedures including, but not limited to, Standard Operating Procedures, Analytical Methods, Development Manufacturing Batch Records and Standard Operating Procedures. br br br b EDUCATION amp EXPERIENCE b br br b Essential br b span span class ts2 nbsp nbsp nbsp span span class ts1 BSc HND degree in relevant discipline or 2-3 years relevant practical experience. br span span class ts2 nbsp nbsp nbsp span span class ts1 2 years experience in downstream processing. br nbsp nbsp nbsp Knowledge of word processing, spreadsheet and database entry skills. br br b Desirable br b nbsp nbsp nbsp Experience in protein purification and scale-up. br nbsp nbsp nbsp Experience in developing performing analytical protein assays e.g. SDS-PAGE ELISA HPLC. br nbsp nbsp nbsp Understanding knowledge of DSP br br br b Key Attributes br span b span class ts4 nbsp nbsp nbsp span span class ts3 Ability to use own initiative and pay close attention to detail br span span class ts4 nbsp nbsp nbsp span span class ts3 Excellent organisational and time management skills br span span class ts2 nbsp nbsp nbsp span span class ts1 Ability to work independently and within a team environment. br span span class ts2 nbsp nbsp nbsp span span class ts1 Possess good problem solving abilities and a high level of communication skills. br span span class ts2 nbsp nbsp nbsp span span class ts1 Ability to plan and perform work assignments, interpret and present data. br br span span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580515http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580515Tue, 6 Oct 2009 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br br b Our client, world class, contract biomanufacturing company offering process development services and pre-GMP and cGMP manufacturing, have an opportunity for a Senior Manufacturing Scientist, due to an exciting period of expansion. br br The post will initially be a 6 month contract with the possibility of extension permanent offer. br br b RESPONSIBILITIES br br b As a member of the GMP Production Department, you will be responsible for the contract manufacture of IMP APIs to GMP standards in the Production Facility. You will perform activities to maintain GMP compliance and assist in the effective technical transfer of projects. br br Responsibilities will include, but not be limited to br nbsp nbsp nbsp Perform activities related to the contract manufacture of Investigational Medicinal Products br nbsp nbsp nbsp Identify and resolve procedural equipment manufacturing problems and deviations, requiring minimal line management direction. br nbsp nbsp nbsp Monitor equipment to ensure continued calibration and maintenance, and that all equipment used in the manufacturing process and any new equipment is validated for its particular use. br nbsp nbsp nbsp Assist in the cross-training of development personnel in GMP procedures br nbsp nbsp nbsp Perform work under periodic line management direction according to documented procedures including, but not limited to, Standard Operating Procedures, Analytical Methods, Development Manufacturing Batch Records and Standard Operating Procedures br br b EDUCATION amp EXPERIENCE b br br b Essential br span b span class ts2 nbsp nbsp nbsp BSc HND degree in Life Science or Biological Science discipline or 3-5 years relevant practical experience. br nbsp nbsp nbsp 3-5 years experience in Mammalian Cell Culture. br nbsp nbsp nbsp Knowledge of word processing, spread Sheet and database entry skills. br br span b span class ts1 Desirable br span b span class ts2 nbsp nbsp nbsp Understanding and experience in Stem Cells Culture. br nbsp nbsp nbsp Understanding and experience of bacterial Fermentation or Mammalian bioreactor vessels. br nbsp nbsp nbsp Understanding knowledge of DSP br br span b span class ts1 Key Attributes br span b span class ts2 nbsp nbsp nbsp Ability to use own initiative and pay close attention to detail br nbsp nbsp nbsp Excellent organisational and time management skills br span span class ts1 nbsp nbsp nbsp Ability to work independently and within a team environment. br nbsp nbsp nbsp Ability to delegate effectively and lead a team br nbsp nbsp nbsp Possess good problem solving abilities and a high level of communication skills. br nbsp nbsp nbsp Ability to plan and perform work assignments, interpret and present data. br br span span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580531http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580531Tue, 6 Oct 2009 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 span.ts3 font-family Symbol font-size 10pt color 000000 span.ts4 font-family Symbol font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br br b Our client, world class, contract biomanufacturing company offering process development services and pre-GMP and cGMP manufacturing, have an opportunity for a Senior Development Scientist Cell Culture , due to an exciting period of expansion. br br The post will initially be a 6 month contract with the possibility of extension permanent offer. br br b RESPONSIBILITIES br br b The Senior Development Scientist Cell Culture will be responsible for leading the management and delivery of a variety of GMP process development projects to quality, time and cost standards. You will provide support to the technical teams in execution of projects and liaise with the sales team in the development of new project definition and contract. br br Your responsibilities will include, but not be limited to br span span class ts3 nbsp nbsp nbsp span span class ts2 Provide a high level of specialist technical knowledge and practical expertise in cell culture processing activities. br span span class ts3 nbsp nbsp nbsp span span class ts2 Monitor equipment to ensure continued calibration and maintenance, and that all equipment used in the development process and any new equipment is suitable for its particular use. br span span class ts3 nbsp nbsp nbsp span span class ts2 Liaise closely with the Director of Operations for the effective planning and transfer of projects from GMP process development to GMP manufacturing according to project. br span span class ts3 nbsp nbsp nbsp span span class ts2 Manage the cell culture process development and assay development functions of the Company. br span span class ts3 nbsp nbsp nbsp span span class ts2 Lead the design and development of GMP compliant cell culture processes and associated activities according to project plans, and perform problem solving troubleshooting of cell culture processes by identifying issues and designing experiments to overcome problems. br span span class ts3 nbsp nbsp nbsp span span class ts2 Ensure that all procedures are documented to appropriate quality standards including, but not limited to, Laboratory Notebooks, Standard Operating Procedures, Bioprocess Methods, Development Manufacturing Batch Records, Deviation Concession Notes. br br span b span class ts1 EDUCATION amp EXPERIENCE br b br b Essential br span b span class ts3 nbsp nbsp nbsp span span class ts2 BSc HND degree in Life Science or Biological Science discipline or 3-5 years relevant practical experience. br span span class ts3 nbsp nbsp nbsp span span class ts2 3-5 years experience in Mammalian Cell Culture. br span span class ts3 nbsp nbsp nbsp span span class ts2 Knowledge of word processing, spreadsheet and database entry skills. br br span b span class ts1 Desirable br span b span class ts3 nbsp nbsp nbsp span span class ts2 PhD in relevant Science discipline or 3-5 years relevant practical experience br span span class ts3 nbsp nbsp nbsp span span class ts2 Understanding and experience in Stem Cells Culture. br span span class ts3 nbsp nbsp nbsp span span class ts2 Understanding and Experience of bacterial fermentation or Mammalian bioreactor vessels. br span span class ts3 nbsp nbsp nbsp span span class ts2 Understanding knowledge of DSP. br br br br span b span class ts1 Key Attributes br span b span class ts3 nbsp nbsp nbsp span span class ts2 Ability to use own initiative and pay close attention to detail br span span class ts3 nbsp nbsp nbsp span span class ts2 Excellent organisational and time management skills br span span class ts4 nbsp nbsp nbsp span span class ts1 Ability to work independently and within a team environment. br span span class ts4 nbsp nbsp nbsp span span class ts1 Ability to delegate effectively and lead a team br span span class ts4 nbsp nbsp nbsp span span class ts1 Possess good problem solving abilities and a high level of communication skills. br span span class ts4 nbsp nbsp nbsp span span class ts1 Ability to plan and perform work assignments, interpret and present data. br span span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582522http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582522Mon, 8 Mar 2010 +0000Salary Commensurate with ExperienceTaysideLocation: Taysidehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582523http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582523Mon, 8 Mar 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 span.ts3 font-family Symbol font-size 10pt color 000000 span.ts4 font-family Symbol font-size 9pt color 000000 span.ts5 font-family Arial font-size 9pt color 000000 -- style head body b span class ts1 SUMMARY br b br Our client, an innovative pharmaceutical company, are currently recruiting for a Formulation Technician to join their Formulation Team based in the south east of England br br b RESPONSIBILITIES br b br span span class ts2 The formulation team is involved in the development of a range of dosage forms from pre-formulation to commercialisation. nbsp Some of the key functions of the department include experimental development of new formulations, manufacture of clinical trial supplies, stability evaluations, compilation of regulatory information and technology transfer to full scale manufacture. Close collaboration with other departments will be required. br br span b span class ts1 EDUCATION amp EXPERIENCE br b br The ideal candidate will be expected to meet the following criteria br br span span class ts4 nbsp nbsp nbsp span span class ts5 A BSc degree or equivalent in a relevant science br span span class ts4 nbsp nbsp nbsp span span class ts5 Good communication skills both verbal and written br span span class ts4 nbsp nbsp nbsp span span class ts5 Basic computer skills i.e. Microsoft Word and Excel br span span class ts4 nbsp nbsp nbsp span span class ts5 High attention to detail br span span class ts4 nbsp nbsp nbsp span span class ts5 Some experience in formulation development and GMP GLP would be preferred, although it is not essential as training will be provided br span span class ts4 nbsp nbsp nbsp span span class ts5 Good time keeping and self-motivation is essential as it is often necessary to work to tight timelines br br br span span class ts1 span body html South EastLocation: South Easthttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582004http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582004Thu, 11 Feb 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582188http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582188Fri, 18 Apr 2008 +0000On ApplicationGrangemouthLocation: Grangemouthhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582189http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582189Mon, 8 Feb 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581022http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581022Fri, 30 Oct 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580828http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580828Wed, 1 Jul 2009 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 span.ts2 font-family Arial font-size 10pt color 000000 -- style head body div align justify b span class ts1 SUMMARY br b br Our client, a global Biotech firm in Central Scotland, who offers contract services and nbsp manufactures products for the bioscience industry, have a new opportunity for a b Product Development Manager. nbsp br b br span div div align justify b span class ts2 In return you will receive a highly competitive salary and benefits package including bonus and pension scheme. br br span div div align justify span class ts1 RESPONSIBILITIES br br div div align justify Reporting to, and working closely with, the Product Development Director b , you will be responsible for the management of the development of new products and or processes within a bio-manufacturing organisation with an international product portfolio. br div div align justify Development and manufacturing capabilities include pilot and large-scale cell culture, polyclonal antibody production, etc. nbsp All manufacturing is carried out according to current Good Manufacturing Practice. br br The candidate will participate and, where required, manage various company wide projects involving interaction with external parties. br br br br b EDUCATION amp EXPERIENCE b br br div div align justify The successful candidate will be qualified to Degree level in an appropriate science. A minimum of five years experience in a similar environment is b essential, b with extensive experience in immunology, antibodies etc. Experience in molecular techniques and project management would be beneficial. br br In addition the successful candidate must have excellent communication skills including both presentation and report writing with an attention to detail , leadership skills and experience, and able to organise themselves and the work of others. br br br span div span class ts1 span body html Central ScotlandLocation: Central Scotlandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580831http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580831Tue, 24 Nov 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581260http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581260Mon, 28 Sep 2009 +0000On ApplicationBerkshireLocation: Berkshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580513http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580513Mon, 5 Oct 2009 +0000Excellent Salary and BenefitsKENTLocation: KENThttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581086http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581086Mon, 5 Oct 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580502http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580502Wed, 10 Sep 2008 +0000On ApplicationWelwyn Garden CityLocation: Welwyn Garden Cityhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581195http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581195Mon, 20 Jul 2009 +0000Excellent Salary DOEWelwyn Garden CityLocation: Welwyn Garden Cityhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580968http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580968Thu, 26 Nov 2009 +0000On ApplicationSouth West EnglandLocation: South West Englandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582406http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582406Fri, 26 Feb 2010 +0000 DOCTYPE HTML PUBLIC - W3C DTD HTML 4.01 Transitional EN html head title Untitled document title meta http-equiv Content-Type content text html charset iso-8859-1 style type text css -- span.ts1 font-family Arial font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br b Our client, a leading Virology Research Company in central London have an opportunity for a Senior QA Associate GLP . br br b RESPONSIBILITIES br b Reporting to the Quality Director, your responsibilities will include, but not be limited to br nbsp nbsp nbsp Ensuring delivery of the Audit Programme. br nbsp nbsp nbsp Ensuring that GLP studies are performed in accordance with GLP regulatory requirements and local laws. br nbsp nbsp nbsp Managing assigned projects, as necessary br nbsp nbsp nbsp Authoring of QA SOP s and review of functional SOPs br nbsp nbsp nbsp Acting as a source of advice and Guidance on Quality GLP GCP laboratory Issues br nbsp nbsp nbsp Assist in implementation of in-house GLP amp GCP laboratory training programme br nbsp nbsp nbsp Implementation of quality audits, both internally and external suppliers and sub-contractors br nbsp nbsp nbsp Implementation of audit reporting system and assurance of timely audit closure br nbsp nbsp nbsp Lead auditor facilitator of audits br nbsp nbsp nbsp Signing QA statement on GLP reports br nbsp nbsp nbsp Completion and closure of audits to defined schedule br br b EDUCATION amp EXPERIENCE br b br The Successful candidate will have br nbsp nbsp nbsp Worked in QA for a number of years including 3 years in a GLP accredited facility br nbsp nbsp nbsp A proven track record in GLP QA with experience of conducting protocol, report, process, critical phase and supplier audits br nbsp nbsp nbsp Sound knowledge of preclinical processes br nbsp nbsp nbsp Excellent attention to detail br nbsp nbsp nbsp Good multi-tasking skills br nbsp nbsp nbsp Experience of GCP Laboratory requirements obtained through audit br br span span class ts1 span body html LONDONLocation: LONDON