http://www.midianls.co.ukLatest Midian JobsTue, 9 Feb 2010 03:05:03 +0000en-ushttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581931http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581931Mon, 8 Feb 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581502http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581502Tue, 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=1581503http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581503Thu, 21 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 Times New Roman font-size 10pt color 000000 span.ts3 font-family Times New Roman font-size 12pt color 000000 span.ts4 font-family Arial font-size 12pt color 000000 span.ts5 font-family Symbol font-size 10pt color 000000 span.ts6 font-family Times New Roman font-size 9pt color 000000 span.ts7 font-family Arial font-size 9pt color 000000 -- style head body div align justify b span class ts1 Summary br b div Our Client, a Global Pharmaceutical Company, seek an exceptional Regulatory CMC Manager based at their Central London Headquarters. nbsp This is a permanent position as a member of a small pharmaceutical technical operations team providing support for the company s international business unit in the manufacture of marketed products for the EU and also for their CMC Research Dept in the development of products and supply of IMP. Office based in London with attendance at CMC Research amp Production sites and at contractor supplier sites throughout the world. br span br div align justify b span class ts1 Responsibilities br b div Reporting to the Senior CMC Manager, you will be an integral member of the Pharmaceutical br Technical Operations team which ensures the reliable supply and quality of commercialised products throughout Europe. nbsp Your primary duties will include, but not be limited to br br span ul type disc li span class ts1 Maintain Regulatory CMC related documentation for ongoing clinical trials span li ul span class ts5 nbsp nbsp nbsp span span class ts1 IMPD-Q sections, storage shipping support statements amp Product Specification Files for IMPs, responses to questions etc. br span ul type disc li span class ts1 Coordinate product support activities at CRO for locally sourced IMP. span li li span class ts1 Provide CMC support for IB updates, contribute to MAA review and to formulation sections of PIP. Prepare CMC related documents and ensure compliance with Marketing Authorisations for marketed products. span li li span class ts1 Contribute to the provision of strategic regulatory advice to colleagues, and to monthly CMC Regulatory Intelligence Reports. span li ul br div align justify b span class ts1 Education amp Experience b br span div ul type disc li span class ts1 Equivalent to degree level in Pharmacy, Chemistry, Biology or other relevant scientific disciplines span li li span class ts1 A least 2 years experience in Regulatory CMC, Manufacturing, Development or Control of Pharmaceutical Products span li li span class ts1 Knowledge pharmaceutical technology related to sterile and non-sterile presentations. span li li span class ts1 Knowledge of requirements of GMP, GLP and GCP span li li span class ts1 Oral and written communication skills span li li span class ts1 Knowledge of EU regulations and Guidelines for CMC for CTA and MAA span li ul br br br br br span class ts1 span body html LONDONLocation: LONDONhttp://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=1580616http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580616Mon, 24 Aug 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 -- style head body b span class ts1 SUMMARY br b br Our client, a leading company it its field of research and development of controlled drugs, have an opportunity for a Quality Assurance Officer. nbsp This position has arisen due to ongoing expansion of the company s operations. nbsp This will be a fixed term 12 month contract. br br b RESPONSIBILITIES br b The company manufactures Active Pharmaceutical Ingredients for both clinical and commercial markets, and Finished Products for commercial, clinical trial, and unlicensed use. br This post offers an exciting opportunity for an enthusiastic Quality Assurance professional. nbsp The position provides a wide and varied scope of responsibility within the company s quality system, and reports to the QA Manager on site. br br br b EDUCATION amp EXPERIENCE br b br The successful candidate will have the following br span span class ts2 nbsp nbsp nbsp span span class ts1 A pharmaceutical background, preferably in Quality Control Assurance, with a strong working knowledge of current Good Manufacturing Practice. nbsp br span span class ts2 nbsp nbsp nbsp span span class ts1 Qualified in a scientific discipline, ideally to degree level. br span span class ts2 nbsp nbsp nbsp span span class ts1 Excellent technical, interpersonal and organisational skills with an eye for detail. nbsp br span span class ts2 nbsp nbsp nbsp span span class ts1 At least two years previous experience in the Quality function would be a definite advantage. br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience in the basic Quality Systems, such as Out-of-Specification OOS and deviation investigations, auditing, and customer complaints would also be a definite advantage. br span span class ts2 nbsp nbsp nbsp span span class ts1 The position will also involve the review of batch records, and so some experience of active ingredient or finished product manufacture would also be beneficial to the role. nbsp br span span class ts2 nbsp nbsp nbsp span span class ts1 A full driving license is essential. br br span span class ts1 span body html South EastLocation: South Easthttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581400http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581400Thu, 14 Jan 2010 +0000Excellent Salary Depending on ExperienceLONDONLocation: LONDONhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581853http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581853Tue, 2 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 div align justify b span class ts1 SUMMARY br b br Our client, a world leading pharmaceutical company, has an opportunity for a Brand Manager, Animal Health to take responsibility for the development and implementation of marketing strategies to support the sale of the company s extensive range of Animal Health amp Veterinary products. nbsp nbsp This position will be a permanent, full time, office based role based in Corby. br br This is a unique and challenging opportunity to join a company in a demanding multinational environment. 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 Brand Manager is responsible for developing and delivering strategic and operational marketing and advertising activity to support sales growth of branded Animal Health amp Veterinary products. Primarily for markets in GB and Ireland although there will be an increasing degree of European marketing work required. Key responsibilities will include undertaking market research, developing marketing materials in-house as well as the commissioning of marketing support from external agencies and suppliers. The role entails the development and delivery of sales support collateral to meet the needs of the company s field based sales forces. br br You will thrive in a demanding working environment, where adherence to tight deadlines and the necessity to deliver added value is second nature. You must be comfortable progressing a number of major projects simultaneously and proactively meeting the marketing needs of a rapidly expanding multi-national organisation. br br br b EDUCATION amp EXPERIENCE br b br div div align justify The ideal candidate will be a dynamic, ambitious and highly motivated marketing professional with either a primary or secondary marketing qualification. You will have a minimum of 3 years marketing experience in the marketing department of a commercial organisation preferably within the pharmaceutical sector although applications from candidates outside the pharmaceutical sector will also be considered. br br br br span div span class ts1 span body html CumbriaLocation: Cumbriahttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581304http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581304Fri, 8 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 -- style head body b span class ts1 SUMMARY br b Our Client, who specialist in the production and sale of antibodies and related products, have an opportunity for a Junior Development Scientist, to join their Purification Team based within Production, Development and Manufacturing facility br br br b RESPONSIBILITIES br b Working in the Purification Team, this lab based role will be actively focused on routine purification of antibody products for customers. nbsp The role will therefore involve customer contact on an occasional basis. br br b EDUCATION amp EXPERIENCE br b Minimum requirements include a biological sciences degree or equivalent with some industrial experience of a protein production and quality controlled environment. A technical understanding of downstream processing techniques including TCF, SEC and Affinity chromatography is required along with experience of automated chromatography systems, ideally Akta Xpress units. A proven track record in troubleshooting is essential along with strong interpersonal, communication and team-working skills. The successful candidate must have a customer focused approach to their work. br br br span span class ts1 span body html CambridgeshireLocation: Cambridgeshirehttp://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=1580507http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580507Thu, 19 Feb 2009 +0000Excellent Salary and BenefitsGrangemouthLocation: Grangemouthhttp://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=1581790http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581790Tue, 2 Feb 2010 +0000Excellent PackageSouth EastLocation: South Easthttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581791http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581791Tue, 2 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 br Our client, a world leading pharmaceutical company, seeks to appoint a Territory Sales Manager to coordinate business in the South of Scotland. 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 Territory Sales Manager will promote and sell a range of animal healthcare and veterinary pharmaceutical products to veterinary practices and key accounts. The primary focus of this role will be to maximise sales of the company portfolio and to develop strong relationships with new and existing clients. br br br b EDUCATION amp EXPERIENCE br b br The ideal candidate will be a self motivated, highly driven individual who has had previous relevant sales experience or has worked with the veterinary profession. Although sales experience is beneficial, knowledge of the veterinary industry is also a key factor to the candidate s success. To this end, experience as a Vet Nurse or a qualification in a life science background would be advantageous, although not critical. Candidates must be willing to travel extensively to fulfil the needs of these roles. The position would be suited to a well organised, professional and friendly candidate who has a strong determination to succeed and enjoys working with other people. br br br span span class ts1 span body html BordersLocation: Bordershttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581153http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581153Thu, 17 Dec 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 -- style head body b span class ts1 SUMMARY br b br Our client, a specialist provider of ADME and pharmacokinetic screening services, are currently recruiting for a Principal Scientist to be responsible for project management of ADMET studies br br b RESPONSIBILITIES br br b As a Principal Scientist, your responsibilities will include, but not be limited to br span span class ts2 nbsp nbsp nbsp span span class ts1 Ensure that experimental protocols and other contractual specifications e.g., report format are followed. br span span class ts2 nbsp nbsp nbsp span span class ts1 Plan and design new studies following consultation with the customer and preparation review of proposals, contracts and reports. br span span class ts2 nbsp nbsp nbsp span span class ts1 Support business development team by acting as scientific advisor in meetings and teleconferences with potential and existing customers. br span span class ts2 nbsp nbsp nbsp span span class ts1 Provide interpretation of results, guidance and scientific support to customers as required. br span span class ts2 nbsp nbsp nbsp span span class ts1 Keep abreast of current knowledge and industry practices in ADMET area br span span class ts2 nbsp nbsp nbsp span span class ts1 Organise internal research and development projects to improve current experimental methods and develop novel processes. br span span class ts2 nbsp nbsp nbsp span span class ts1 Develop laboratory staff in experimental scientific processes. br span span class ts2 nbsp nbsp nbsp span span class ts1 Act as the scientific contact for the laboratory supervisors and assist in troubleshooting as required br span span class ts2 nbsp nbsp nbsp span span class ts1 Take an active interest in the maintenance and development of laboratory processes to ensure that all data produced is of a consistently high quality. br span span class ts2 nbsp nbsp nbsp span span class ts1 Participate in quality activities br br br b EDUCATION amp EXPERIENCE br b br span span class ts2 nbsp nbsp nbsp span span class ts1 Ph.D. or equivalent experience in relevant scientific discipline. br span span class ts2 nbsp nbsp nbsp span span class ts1 3 or more years experience in the biotechnology or pharmaceutical industry. br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience of at least one area of i in vitro i ADMET PK is essential br span span class ts2 nbsp nbsp nbsp span span class ts1 Highly motivated 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 Able to communicate effectively with customers and within a team environment. br span span class ts2 nbsp nbsp nbsp span span class ts1 Perform ADMET or other biological assays competently. br span span class ts2 nbsp nbsp nbsp span span class ts1 Good understanding of quantitative analysis using LC-MS or similar. br span span class ts2 nbsp nbsp nbsp span span class ts1 Extensive knowledge of absorption, distribution, metabolism, excretion and toxicology. br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience of working in a commercial environment, preferably a contract research organization. br span span class ts2 nbsp nbsp nbsp span span class ts1 Must be able to undertake travel to visit clients br br span span class ts1 span body html CHESHIRELocation: CHESHIREhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580832http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580832Wed, 25 Nov 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580503http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580503Fri, 18 Apr 2008 +0000On ApplicationGrangemouthLocation: Grangemouthhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580504http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1580504Fri, 4 Jul 2008 +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 Symbol font-size 10pt color 000000 span.ts3 font-family Calibri font-size 8pt color 000000 span.ts4 font-family Calibri font-size 10pt color 000000 -- style head body div align justify b span class ts1 SUMMARY br b Our client, a b world leading b b pharmaceutical company b , has an outstanding opportunity for an b Instrument Technician. nbsp b This will be a permanent role with shift work involved. br br b In return our client offers a challenging career in a supportive environment with excellent prospects for training, development and career progression. b br br br b REQUIREMENTS br span div ul type disc li div align justify span class ts1 Works as part of a team and is responsible for the installation, maintenance and calibration of instrumentation systems in the factory. span b li li span class ts1 Provision of maintenance and repair service for pneumatic and electronic instruments and advise on maintenance routines. span li li span class ts1 Provision of an installation and commissioning service on new equipment and modify existing equipment. span li li span class ts1 Advise users on correct operation and use of instruments and process control systems. span li li span class ts1 Responsible for correct implementation of routine maintenance procedures. span li li span class ts1 Can suggest modifications of instruments, systems or work methods to the Team Manager. span li ul div ul type disc li div align justify span class ts1 EDUCATION amp EXPERIENCE span li ul div ul type disc li span class ts1 Completed either an appropriate instrument engineering apprenticeship or relevant course. span li ul type disc li span class ts1 Has a proven competency in hazardous area equipment maintenance. span li ul ul ul type disc li div align justify span class ts1 The ability to interpret circuit diagram and other engineering drawings, perform fault diagnosis, analyse data, use computer systems eg EPMS and perform appropriate administration duties. span li li span class ts1 Understand and apply Company and Site procedures and standards. span li ul br br div div align justify span class ts1 span body html MontroseLocation: Montrosehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581501http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581501Fri, 15 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 div Our Client, a Global Pharmaceutical Company, seek an exceptional Regulatory CMC Manager based at their Central London Headquarters. nbsp This is a permanent position as a member of a small pharmaceutical technical operations team providing support for the company s international business unit in the manufacture of marketed products for the EU. Office based in London with attendance at CMC Research amp Production sites and at contractor supplier sites throughout the world. br br div align justify b Responsibilities br b div Reporting to the Senior CMC Manager, you will be an integral member of the Pharmaceutical br Technical Operations team which ensures the reliable supply and quality of commercialised products throughout Europe. nbsp Your primary duties will include, but not be limited to br 1. nbsp nbsp nbsp Prepare CMC related documents and ensure compliance with Marketing Authorisations for marketed products br span ul type disc li span class ts1 Maintain Product Technical Files, span li li span class ts1 Prepare variations, rewrite MAA sections, span li li span class ts1 Review batch manufacturing documents, identify regulatory action, span li li span class ts1 Review CMO change requests, span li li span class ts1 Prepare Annual Product Quality Reviews, span li li span class ts1 Organise product support activities at CRO for locally manufactured products, span li li span class ts1 Prepare stability reports span li ul br 2. nbsp nbsp nbsp Manage CMC development projects for commercial products br ul type disc li span class ts1 Prepare project proposals amp justifications, span li li span class ts1 Develop project requirement specifications, span li li span class ts1 Identify service providers span li ul br 3. nbsp nbsp nbsp Contribute to the provision of strategic regulatory advice to colleagues. br br 4. nbsp nbsp nbsp Provide monthly activity reports for Senior Management. br br 5. nbsp nbsp nbsp Support clinical studies using marketed products br ul type disc li span class ts1 Review IMPD-Q, span li li span class ts1 Source placebo comparator products, span li li span class ts1 Update IB span li ul br div align justify b Education amp Experience b br div ul type disc li span class ts1 Equivalent to degree level in Pharmacy, Chemistry, Biology or other relevant scientific disciplines span li li span class ts1 A least 2 years experience in Regulatory CMC, Manufacturing or Development of Pharmaceutical Products span li li span class ts1 Knowledge pharmaceutical technology related to sterile and non-sterile presentations. span li li span class ts1 Knowledge of requirements of GMP, GLP and GCP span li li span class ts1 Oral and written communication skills span li li span class ts1 Knowledge of EU regulations and Guidelines for CMC for CTA and MAA span li ul br br span class ts1 span body html LONDONLocation: LONDONhttp://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=1581762http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1581762Thu, 10 Dec 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 Times New Roman font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br br b Our client, a preclinical CRO have an exciting new opportunity for a Preclinical QA Study Manager to join their expanding scientific team, adding quality amp value to their expanding research services. br br This position would suit an experienced Project Leader or Study Director looking to move into a more strategic Quality role. br br br b RESPONSIBILITIES br b br In this role you would be working closely with the global quality team and responsibilities will include, but not be limited to br span span class ts2 nbsp nbsp nbsp span span class ts1 Working closely with study directors to prepare SOPs and appropriate documentation for their studies. br span span class ts2 nbsp nbsp nbsp span span class ts1 Creating and maintaining quality systems br span span class ts2 nbsp nbsp nbsp span span class ts1 Quality control of documentation and reports br span span class ts2 nbsp nbsp nbsp span span class ts1 Quality control of data entered into spreadsheet formats br span span class ts2 nbsp nbsp nbsp span span class ts1 Training scientific staff to implement procedures set out in SOPs br span span class ts2 nbsp nbsp nbsp span span class ts1 Ensuring that risk assessments are complete and up to date for all laboratory processes br br br b EDUCATION amp EXPERIENCE br b br span div align justify span class ts1 The ideal candidate will be a highly motivated self-starter experienced in a GLP working environment within a contract research organisation or pharmaceutical setting. nbsp They must also have the following b essential b qualifications and experience br span div span class ts2 nbsp nbsp nbsp span span class ts1 Degree in a relevant scientific discipline br span span class ts2 nbsp nbsp nbsp span span class ts1 4-5 years laboratory experience br span span class ts2 nbsp nbsp nbsp span span class ts1 A flexible approach to documentation SOP implementation br span span class ts2 nbsp nbsp nbsp span span class ts1 Exceptional attention to detail br span span class ts2 nbsp nbsp nbsp span span class ts1 Excellent written and oral communication skills br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience of working on their own initiative and working within a multidisciplinary team br br br Knowledge of COSHH and lab safety experience would be an advantage. br br span span class ts1 span body html GlasgowLocation: Glasgow