http://www.midianls.co.ukLatest Midian JobsFri, 30 Jul 2010 12:31:02 +0000en-ushttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584376http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584376Mon, 9 Nov 2009 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584969http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584969Thu, 10 Jun 2010 +0000On ApplicationWelwyn Garden CityLocation: Welwyn Garden Cityhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584915http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584915Wed, 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 Arial font-size 10pt color 000000 span.ts2 font-family Symbol font-size 10pt color 000000 span.ts3 font-family Calibri font-size 10pt color 000000 span.ts4 font-family Calibri font-size 11pt color 000000 span.ts5 font-family Times New Roman font-size 11pt 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 b br 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 of point of care tests. 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 b Responsibilities br b div div align justify Responsible for the development of point of care tests you will be expected to participate in the provision of a high quality development service for external customers as well as internal projects br span div ul type disc li div align justify span class ts1 The role will be laboratory based and will involve working within a project team on a specific project. span li li span class ts1 You will also be expected to work unsupervised using your own initiative to design and implement individual experiments. span li li span class ts1 The job will also include the analysis of subsequent data, processing and presentation of data in required format, contribution to internal project meetings as well as communication and reporting to external customers. span li li span class ts1 You will be expected to work within the companies ISO 9001 2000 development and reporting system and play a proactive role discussing results and general project planning. span li ul br div div align justify b Education amp Experience b br div Essential br ul type disc li span class ts1 Good BSc or PhD in Biochemistry, Biotechnology or related subject span li li span class ts1 Experience with commercial development of products and working within goal orientated culture span li li span class ts1 Knowledge and experience working with Excel span li li span class ts1 Enthusiastic and dynamic individual span li li span class ts1 Team orientated with excellent communication skills span li li span class ts1 Good report-writing skills span li li span class ts1 Professional person who can represent the company in interactions with customers span li ul br Desirable br ul type disc li span class ts1 Good understanding and experience of working to ISO 9001 2000 span li li span class ts1 Experience of working in a highly regulated industry span li li span class ts1 Experience of lateral flow technology span li ul br nbsp nbsp nbsp nbsp nbsp nbsp nbsp nbsp nbsp br br br div align justify 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=1584916http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584916Tue, 1 Jun 2010 +0000On ApplicationEast EnglandLocation: East Englandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582801http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1582801Tue, 2 Mar 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586190http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586190Fri, 23 Jul 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584968http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584968Wed, 9 Jun 2010 +0000On ApplicationSouth West EnglandLocation: South West Englandhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584265http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584265Fri, 16 Apr 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 Verdana font-size 10pt color 000000 span.ts4 font-family Symbol font-size 10pt color 000000 -- style head body b span class ts1 SUMMARY br span b br span class ts2 Our client, a leading b Virology Research b Company in central London have an opportunity for a b Preclinical Study Director b , to be responsible for all aspects of assigned preclinical studies, in support of clinical studies br br span b span class ts1 RESPONSIBILITIES br b br Reporting to the span span class ts3 Director of Preclinical Operations, your responsibilities will include, but not be limited to br span div align justify span class ts4 nbsp nbsp nbsp span span class ts1 Conducting studies according to the agreed protocol, timeline and budget, in line with GLP standards br span div div align justify span class ts4 nbsp nbsp nbsp span span class ts1 Developing the protocol and services within studies, in line with client requirements. br span span class ts4 nbsp nbsp nbsp span span class ts1 Ensuring studies are conducted safely, ethically and appropriately in compliance to agreed protocols and quality standards. br span span class ts4 nbsp nbsp nbsp span span class ts1 Introduce new techniques and procedures to maintain scientific capability in line with competitors. br span span class ts4 nbsp nbsp nbsp span span class ts1 Providing scientific and professional leadership. br span span class ts4 nbsp nbsp nbsp span span class ts1 Designing and executing scientific experiments. Propose, develop and validate new methodologies. Originate and develop new project ideas. br span span class ts4 nbsp nbsp nbsp span span class ts1 Simultaneously manage multiple studies as a Study Director br span span class ts4 nbsp nbsp nbsp span span class ts1 Effective project management of studies as appropriate, ensuring that all resources, including staffing requirements are allocated appropriately and all parties are fully informed. br span span class ts4 nbsp nbsp nbsp span span class ts1 Keeping abreast of current scientific developments and new techniques by maintaining their training records and general reading br span span class ts4 nbsp nbsp nbsp span span class ts1 Writing reports, manuscripts, SOP s and other appropriate documentation in line with company standards and where applicable, using company templates br span span class ts4 nbsp nbsp nbsp span span class ts1 Effectively manages all direct reports, ensuring effective performance management in line with best practice and company policy. br span span class ts4 nbsp nbsp nbsp span span class ts1 Maintaining customer satisfaction of both internal and external clients and stakeholders br span span class ts4 nbsp nbsp nbsp span span class ts1 Managing key accounts and assist in business development activities to achieve high level of client satisfaction and therefore ensuring repeat business opportunities. br br br div b EDUCATION amp EXPERIENCE br b br div align justify A successful study director will have excellent planning and organisational skills with an ability to multitask and meet tight deadlines. They will also be a motivator of people and be able to manage and supervise effectively. This is a client facing role therefore strong communication skills with are essential. A minimum of three years successful study direction is required in one or more of the following areas br div b testing anti-virals, biological assays, in vitro and in vivo. br b br span span class ts1 span body html LONDONLocation: LONDONhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584458http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584458Wed, 28 Apr 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 br b Our client, and innovative diagnostics company, are seeking applicants for the position of b Reagent Development Scientist b . nbsp Reporting to the Assay Development Manager the successful candidate will be responsible for the development of immunodiagnostic reagents that will be optimized for use with the client s detection technology. br br b RESPONSIBILITIES br b br Your primary responsibilities will include br span span class ts2 nbsp nbsp nbsp span span class ts1 Development of procedures for the conjugation of antibodies to a variety of fluorescent and phosphorescent labels and the immobilization of antibodies and antigens to thermoplastic solid supports. br span span class ts2 nbsp nbsp nbsp span span class ts1 Development of reagent formulations for dry format microfluidic based assays. br span span class ts2 nbsp nbsp nbsp span span class ts1 Contribute to the development of novel assay formats based on optical detection technology br span span class ts2 nbsp nbsp nbsp span span class ts1 Implement protocols and procedures which are compatible with current manufacturing practices. br span span class ts2 nbsp nbsp nbsp span span class ts1 Work within the established Quality Management System and to GLP and ISO13485 standards. br span span class ts2 nbsp nbsp nbsp span span class ts1 Representing the Company in relationships with development partners and suppliers. br br br b EDUCATION amp EXPERIENCE br b br Candidates should have a PhD in chemistry, biochemistry or an alternative biomedical science subject with good practical knowledge of the techniques for antibody purification, conjugation and immobilization. nbsp Applicants should also be familiar with immunoassay design and development and data analysis packages such as Excel and Origin. nbsp br br Minimum 5 years experience in the commercial development of immunodiagnostic reagents. br br Experience of micro-dispensing for microfluidic based assays and whole blood filtration is desirable but not essential. br br span span class ts1 span body html LONDONLocation: LONDONhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585046http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585046Thu, 13 May 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, who specialises in the production and sale of antibodies and related products have an opportunity for a Senior Imaging Technician within their Product Development amp Manufacture facility. br br In return our client offers a challenging career in an expanding dynamic company with excellent salary and benefits package. br br b RESPONSIBILITIES br b Working closely with the Imaging Scientists, the Imaging Technician will be responsible for br span span class ts2 nbsp nbsp nbsp span span class ts1 Performing immunofluorescence and immunohistochemical staining techniques, br span span class ts2 nbsp nbsp nbsp span span class ts1 Producing high quality results which they can interpret, analyse and record br span span class ts2 nbsp nbsp nbsp span span class ts1 Assisting with the everyday running of the Imaging Lab. br br br b EDUCATION amp EXPERIENCE br b You will be educated to degree level or equivalent in a biological science. Candidates will have previous laboratory experience. Working knowledge of immunofluorescence and immunohistochemistry is desirable. Experience of any other immunological laboratory techniques would also be an advantage. br br br br span span class ts1 span body html CambridgeshireLocation: Cambridgeshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585393http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585393Thu, 10 Jun 2010 +0000On ApplicationWelwyn Garden CityLocation: Welwyn Garden Cityhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586189http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586189Thu, 1 Jul 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 Our client, a world leading pharmaceutical company are currently recruiting for a b Senior Process Engineer b . nbsp This position will be a 12 month Fixed Term Contract. br br br b RESPONSIBILITIES br b Supporting the Process Engineering Team Leader to provide process engineering expertise to Maintenance, Projects, Production, EHS and Development departments within a cGMP environment. nbsp Your responsibilities will include, but not be limited to br br span div div align justify span class ts2 nbsp nbsp nbsp span span class ts1 Provide Process Engineering Resource for Capital Projects e.g. Calculations, Data Sheets, and Commissioning , Safety Reviews and Process Plant Trouble Shooting as required. br span span class ts2 nbsp nbsp nbsp span span class ts1 Check and approve calculations and other documents by other Process Engineers as required. br span span class ts2 nbsp nbsp nbsp span span class ts1 Work closely with the Production Departments to assess and prioritise opportunities to improve processing efficiency, environmental health safety quality performance and labour efficiency through engineering improvements. br span span class ts2 nbsp nbsp nbsp span span class ts1 Evaluate and cost engineering work, modifications or proposals as required by other departments. Raise expenditure authorisations and carry out engineering work within agreed revenue and capital expenditure budgets and approvals. br span span class ts2 nbsp nbsp nbsp span span class ts1 Manage and motivate project resource, when required, to achieve a high level of productivity and efficiency. This will include management of contractors carrying out Installation work including Method Statement Risk Assessment review approval, accepting Permits to Work incl. Hot Work and ensuring any additional CDM requirements are fulfilled. br span span class ts2 nbsp nbsp nbsp span span class ts1 Carry out hazardous area classification and pressure relief reviews as required by Projects and periodic reviews. br span span class ts2 nbsp nbsp nbsp span span class ts1 Work effectively with other factory managers. Communicate and negotiate with suppliers, contractors, local government officials, factory inspectors and regulatory body representatives auditors etc. br br div div align justify b EDUCATION amp EXPERIENCE br b The successful candidate should meet the following criteria br span div div align justify span class ts2 nbsp nbsp nbsp span span class ts1 Degree in Chemical Engineering or alternative degree with appropriate training and experience with Chartered Engineer status or equivalent experience . br span span class ts2 nbsp nbsp nbsp span span class ts1 Considerable experience of chemical plant, pipe-work, structures and knowledge of service providing equipment br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience of managing engineering projects. br span span class ts2 nbsp nbsp nbsp span span class ts1 Experience in a pharmaceutical, food or chemical plant environment. br br br span div div align justify span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584602http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584602Thu, 20 May 2010 +0000On ApplicationSussexLocation: Sussexhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584803http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584803Mon, 8 Mar 2010 +0000Salary Commensurate with ExperienceTaysideLocation: Taysidehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584726http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1584726Wed, 26 May 2010 +0000On ApplicationNorth WestLocation: North Westhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1583456http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1583456Thu, 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 Manager to join their expanding scientific team, adding quality amp value to their expanding research services. br br This position would suit an experienced Preclinical Study Director with Quality experience looking to move into a 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 you will be solely responsible for creating the GLP quality system. nbsp Additional 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 br span span class ts1 span body html GlasgowLocation: Glasgowhttp://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=1586186http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586186Fri, 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=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=1586188http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586188Thu, 10 Jun 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 world leading pharmaceutical company are currently recruiting for a b Development Chemist b to develop new processes improve existing processes and support production by means of problem solving and trouble shooting. nbsp The position has become available due to internal promotion br br In return you will receive an excellent salary and benefits package along with the opportunity to develop and progress within the role. br br b RESPONSIBILITIES br b Reporting to the Development Project Manager, your responsibilities will include, but not be limited to br br nbsp nbsp nbsp To identify potential routes to new products and plan and conduct experiments to assess the viability of processes and process improvements. br nbsp nbsp nbsp Carry out plant investigations to solve production problems or improve processes. br nbsp nbsp nbsp Develop processes - identifying and optimising the key process parameters. br nbsp nbsp nbsp Assist in the development of analytical methods and prepare IPC s. br nbsp nbsp nbsp Ensure the safe and effective scale-up of processes and process modifications to SSM and or full-scale plant. br nbsp nbsp nbsp Provide technical and analytical support during process commissioning and after transfer of processes to production. br nbsp nbsp nbsp Supervise staff or lead teams where required. br nbsp nbsp nbsp Follow the company procedures relating to SHE, quality, controlled drug regulations and cGMP. br nbsp nbsp nbsp Maintain a record of all experimental work and produce development and technical reports, SOP s and other documents. br br b EDUCATION amp EXPERIENCE br b The successful candidate should meet the following criteria br nbsp nbsp nbsp BSc Hons Chemistry and significant relevant experience or PhD in synthetic organic chemistry. br nbsp nbsp nbsp Sound knowledge of synthetic organic chemistry. br nbsp nbsp nbsp A good knowledge of laboratory process development within the pharmaceutical bulk actives fine chemicals industry. br nbsp nbsp nbsp Experience of scale up of organic processes to pilot plant or full scale production. br nbsp nbsp nbsp Team player. br nbsp nbsp nbsp Excellent practical skills. br nbsp nbsp nbsp Problem solving skills. br br span span class ts1 span body html EdinburghLocation: Edinburghhttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585395http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1585395Mon, 28 Jun 2010 +0000On ApplicationHertfordshireLocation: Hertfordshirehttp://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586187http://www.job-tv.co.uk/websites/midian/VacancyDetails.asp?VacancyID=1586187Tue, 23 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 offering services in formulation development and clinical manufacture across all the main dosage forms is currently recruiting for a Qualified Person br br b RESPONSIBILITIES br b br As a Qualified Person reporting to the CEO your responsibilities will include br nbsp nbsp nbsp Responsible for Quality Assurance and release of Clinical Supplies and Specials for specific projects. Liaises with Business Development Director, Chief Operations Officer and Chief Science Officer. br nbsp nbsp nbsp Perform Qualified Person certification. br nbsp nbsp nbsp Keep up to date with current and proposed pharmaceutical regulations in the EU and USA. br nbsp nbsp nbsp Monitor, trend and, if necessary, correct any Quality aspects pertaining to the CMC projects including responding to customer complaints and advise management on any GMP quality deficiencies as appropriate br nbsp nbsp nbsp Authorise, or designate responsibility for the approval of Batch documentation laboratory records prior to release to a client br nbsp nbsp nbsp Assist in GMP training. br nbsp nbsp nbsp Perform or manage supplier and sub contractor audits and monitor performance. br nbsp nbsp nbsp Attend Quality Review Meetings br br b QUALIFICATIONS br b br Eligible as a Qualified Person in accordance with Directive 2004 27 EC for IMPs br Possessing a qualification in a life-science related subject br br b SKILLS amp EXPERIENCE br b nbsp nbsp nbsp At least 3 years work experience practicing as a Qualified Person in a relevant manufacturing environment. br nbsp nbsp nbsp Well versed in requirements of the EU CT Directive and its importance within a commercial or clinical manufacturing operation. br nbsp nbsp nbsp Experience of working to MHRA amp FDA standards br nbsp nbsp nbsp Proven record of operating effectively in a Quality leadership role br nbsp nbsp nbsp First hand experience of diverse dosage forms with particular expertise in sterile products manufacture is essential br nbsp nbsp nbsp An enthusiastic professional who is passionate about Quality br nbsp nbsp nbsp Has a good understanding of how CMC fits into the drug development process br nbsp nbsp nbsp An authoritative and credible leader who is able to influence and win the respect of their peers, colleagues and clients. br br br span span class ts1 span body html NOTTINGHAMSHIRELocation: NOTTINGHAMSHIREhttp://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 England