http://quantacs.contentedmanagement.co.uk/jobs en-GB Quanta Consultancy Services Ltd, 1993 - 2008 Thu, 29 Jul 2010 12:27:22 GMT Thu, 29 Jul 2010 12:27:22 GMT Raccoom rss generator, website http://raccoom.sytes.net, email chrisdarebell@msn.com 120 My client is a global Biopharmaceutical organisation; they require an experienced Site QMS Champion for a long term contract position at their campus in East Anglia. The purpose of the role is to manage the implementation on site of the corporate Quality Management System and tracks implementation and reports on progress. Key Responsibilities: * Represents the site at QMS Champion meetings and acts as liaison between site and Corporate Quality Operations Manages review on site of new corporate standards, to deadlines * Supports process owners in facilitation of gap analysis and development of remediation plans, to deadlines * Supports process owners with implementation/remediation, as required * Tracks each stage of implementation and reports metrics on and off site Relationships: * Frequent internal contacts across the site and with Genzyme Corporate Quality Operations * Builds good working relationships with process owners * Responds to requests for information as required Scope/Impact: * Work is not supervised directly but reviewed against project plans and results. Independently determines and develops solutions to identified problems. Work is reviewed upon completion for adequacy in meeting objectives. * Organises time to meet short and medium term deadlines set by others. * Will receive guidance from Manager initially * Assists in meeting site and corporate objectives Knowledge, Skills and Experience Required: * Typically a graduate or equivalent * Prior experience of working within a quality management system an advantage * Demonstrated ability to work to, and manage projects to, deadlines * Knowledge of cGMP preferred This is a fantastic opportunity to work with a growing organisation with cutting edge technology and drugs; to further your professional experience. Please apply now for more information on this long term opening, paying competitive rates. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/site-qms-champion-east-anglia-uk-j011496 Quanta Consultancy Services Ltd Thu, 29 Jul 2010 12:27:22 GMT http://quantacs.contentedmanagement.co.uk/2894 Quanta?s client, a world leading international pharmaceutical company, are seeking x2 Regulatory CMC Specialists / Product Specialists for the department of Network CMC (Chemistry Manufacturing & Control) to be based at their facility in the Netherlands. The Network CMC team is responsible to carry out regulatory activities that are needed in the context of site changes, in particular with respect to chemical/pharmaceutical aspects of the submissions. Network CMC is part of Quality Assurance and Pharmaceutical CMC. Tasks and Responsibilities: * Prepares CMC documentation for international submissions in accordance with local dossier requirements. * Takes part in the review and release of CMC documents in accordance with the applicable procedures. * Supervises the compilation of CMC dossiers. * Answers questions from health authorities and coordinates the Agency Response process. * Is conversant with relevant, worldwide registration requirements. * Is conversant with literature relevant to the projects and products assigned to him/her. * Makes proposals to the organization with regard to variations of chemical/pharmaceutical documents following questions from authorities. Consults wit the departments involved. * Takes the initiative for and coordinates additional studies which are performed by the chemical/pharmaceutical disciplines. * Has contacts with other staff of local companies and other sister companies. * Sees to planning, coordination and implementation of all the tasks related to his/her project. Requirements: * MSc (Chemistry, Physics, Pharmacy, Analytical Chemistry) or BSc with multiple years of experience * Minimum of 2 year registration experience in CMC. * Good command of written and spoken English. * Command of Dutch language is an advantage, but no must * Good editing skills. * Has good social skills and is a good team player. * Communicative, assertive and persuasive person * Good organizational skills The position will start with a 12 months contract, but as the project is expected to be continued, it is very likely that the contract may be extended for a period of about 3 to 4 years. Offering competitive rates of pay, please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/x2-regulatory-cmc-specialists-holland-europe-j011492 Quanta Consultancy Services Ltd Wed, 28 Jul 2010 12:27:22 GMT http://quantacs.contentedmanagement.co.uk/2893 A major Telecoms Vendor requires an A System Design Engineer within SON (Self Organised Network). The desired candidate would work within the New OSS R&D Team as a SON System Design Engineer. This contract role provides an opportunity for an experienced System Design Engineer to work as a System Designer within SON (Self Organised Network). The Work will be based in their Swedish based R&D Office. The role and responsibilities: *To work on the LTE O&M (operation & maintenance) solution Design *To be responsible of the operation & maintenance analysis on the difference between the traditional and Self organised networks, *To take responsibility for the key technologies within SON *Educate & Mentor the System Engineers & Developers Ideal level of experience: * To have a high level of understanding of radio network trends within the Next Generation of OSS * A high level of experience within Radio Network maintenance. * To be familiar with 3GPP and MGMN within SON * Experience of LTE O&M design *Must of worked with an R&D environment *A good understanding of Radio Network and network maintenance trends *Fluent in English *To be eligible to work in Sweden http://quantacs.contentedmanagement.co.uk/jobs/telecoms-jobs/senior-system-design-engineer-within-son-sweden-scandinavia-j011487 Quanta Consultancy Services Ltd Tue, 27 Jul 2010 16:27:24 GMT http://quantacs.contentedmanagement.co.uk/2890 QA Specialist required supporting European new build project. Working within the Upstream Processing area of this biotech facility you will be providing in field QA Support Your role and responsibilities will be varied and will include: *Preparing documentation required for the test execution *Complete any change control documentation required (CCR's, Deviations, etc) *Review completed documentation in advance of final review by Area QA lead *Write the final OQ reports Skills/experience required: *Prior QA experience gained working within a pharmaceutical or biophrma environment *Experience with C&Q a distinct plus This contract opportunity is to start ASAP and will run until the end of the year. http://quantacs.contentedmanagement.co.uk/jobs/biotechnology-and-biopharma-jobs/qa-field-support-engineer-geneva-switzerland-europe-j011429 Quanta Consultancy Services Ltd Fri, 23 Jul 2010 16:27:25 GMT http://quantacs.contentedmanagement.co.uk/2887 A major Telecoms Vendor has an urgent requirement for a Senior System Design Engineer in OAM/O&M Solution. As a Senior System Design Engineer you will be responsible for analysing the operation and maintenance scenarios within configuration, performance and fault management. As the successful Senior System Design Engineer you will be required to interact with customers and participate in the design of solutions within multi-mode BTS OAM/O&M technology area. The work will be based in Sweden and is an opportunity to work with an organisation that has a strong focus on innovation within the Telecommunications industry. The role and responsibilities: * Participating in multi-mode BTS OAM solution design * Analysing operation and maintenance (OAM, O&M) scenarios within configuration management, performance management and fault management * Responsible for developing and seeking key technologies in multi-mode BTS OAM * Responsible for understanding the main problem when operators maintain multi-mode BTS OAM. * Ability to mentor and instruct System Engineers and Developers Ideal level of experience: * 10 years experience of Radio Network maintenance * Understanding of Radio Network trends and Network maintenance trends * Knowledge and a familiarity of RAN OAM/O&M design * Understanding of the organisational structure of operation and maintenance systems within an operators environment * Experience of mentoring and instructing others or running a team Candidates will need to demonstrate: * Free movement around the European Community * A Master of Science or equivalent in ICT related subjects * Excellent organisational skills accompanied with high communication skills * Driven, ambitious and tenacious personality * A strong background and experience in Telecoms http://quantacs.contentedmanagement.co.uk/jobs/telecoms-jobs/senior-system-design-engineer-om-sweden-scandinavia-j011477 Quanta Consultancy Services Ltd Thu, 22 Jul 2010 12:27:43 GMT http://quantacs.contentedmanagement.co.uk/2886 A major European telecoms provider based in Vienna is seeking to hire an experienced Contract Oracle Applications DBA. The Company has recently undergone a major re-organisation and is also upgrading from Oracle 9 to Oracle 11.2. The successful Oracle Apps DBA will need to have experience of working in a busy environment with the many challenges that a large Oracle production system demands. The working language is English though it would be beneficial to also have knowledge of German. Essential skills: - Oracle 11.2 - Oracle 9 - Previous Oracle migration experience - English Desired skills: - German Note: - This is potentially a long term contract assignment and hence if you are an Oracle Apps DBA seeking to stay in one location for a long period then this could be an ideal opportunity for you. http://quantacs.contentedmanagement.co.uk/jobs/telecoms-jobs/oracle-applications-dba-vienna-austria-europe-j011471 Quanta Consultancy Services Ltd Wed, 21 Jul 2010 12:27:27 GMT http://quantacs.contentedmanagement.co.uk/2884 We require an MES Consultant with experience of writing MBR's, reviewing and updating SOP's, completing on-flow support, updating documents and potentially completing on-site training with users. This position is for an MES deployment that is due to conclude later in 2010 and will require a consultant to offer ongoing support beyond the initial contract term. This position will require the successful consultant to be a self-starter and strong team player to successfully complete this contract. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/mes-consultant--ireland-eire-europe-j011472 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 16:27:28 GMT http://quantacs.contentedmanagement.co.uk/2881 An exceptional contract opportunity has arisen for a Program Manager within a global Biotech organisation. This position will be based at their Irish manufacturing facility and accountabilities will include: * Leads cross-functional teams in projects such as continuous improvement, technology transfer, new product introduction, business integration of new products. * Leads the technology transfer of a product from one manufacturing location/scale to another, both within and between sites. * Translates customer needs into defined, approved project scope statements; works with project sponsor(s) and stakeholders within and across sites to quantify resource requirements in support of successful project delivery * Establishes detailed project plan, including completion dates and project workload sequences; drives execution of project tasks in line with agreed scope and time lines * Key Internal Contacts: Quality Control team; Manufacturing and Packaging management teams; Finance; Planning Manager; Regulatory Affairs team; Quality Assurance team; Tec Dev team; Process Engineering; Product Management * Key External Contacts: CMC team leader; Business Unit programme managers, Operations Project Managers. Experience required: * Degree educated in Life Science or Engineering * In depth experience of Program Management in a GMP / FDA regulated environment * Ideally knowledge of oral dosage and/or aseptic fill/finish manufacturing * Experience of analytical methods and associated technical transfer an advantage * A proven track record in the ability to transfer goals and objectives into measurable plans This is a long term contract opening, offering competitive rates for a rapidly expanding Biopharmaceutical organisation. Please apply now for this exciting and challenging position. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/program-manager--ireland-eire-europe-j011473 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 16:27:28 GMT http://quantacs.contentedmanagement.co.uk/2882 A multi-national pharmaceutical organisation requires a SHE specialist (Occupational Health) to work at their manufacturing campus in Boxmeer. The main aim of this role is to set up health plan, ergonomics projects, occupational health advice, sets up plan. Tasks will include: * The implementation of SHE ? inspections. * Ergonomic consultant at project/construction applications applications and modifications. * Preparing and developing Arbo-policy proposals. * Giving instructed and instructions on SHE area. * The implementation of SHE tasks within the organisation. * Developing and preparing ergonomic policy plan. Experience required: * Training Post-HBO industrial hygiene or higher security knowledge; * Knowledge of and experience with health plans, PMO, ergonomics * Strong communicative skills, team player. Please apply now for more information on this freelance contract position. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/hse-specialist-(dutch-speaking)-oc-health-other-holland-europe-j011474 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 16:27:28 GMT http://quantacs.contentedmanagement.co.uk/2883 Javascript Developer required to join a large Financial Software development organisation. Based in Milton Keynes you will join an established and talented team of Java script developers developing award winning web applications and financial services business solutions. The Role: * Working with a team of Software Developers, Business Analysts and Software Testers, to produce complex solutions to client requirements, utilising Object Oriented techniques. * Build strong, on-going relationships with clients and customers * Provide technical expertise and knowledge throughout the team and organisation. Essential Skills and Experience: * Proven Java script development experience * Knowledge of Hibernate * Knowledge of Dojo would be an advantage * OO design and development * Attention to detail, communication and flexibility are a must. If you would like more information on this initial 6 month contract position please forward your CV to Joanna@quanta-cs.com http://quantacs.contentedmanagement.co.uk/jobs/information-technology-jobs/javascript-developer-south-east-uk-j011470 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 12:27:30 GMT http://quantacs.contentedmanagement.co.uk/2878 My client, a global pharmaceutical organisation is building a European Distribution Head Quarters and requires an experienced Commissioning Lead for a 12 month contract. This is a Greenfield project and will be focussed on Cold Chain GMP requirements. It is expected that you can lead and drive projects but also be happy to be hands on throughout the project life cycle. You will be responsible for: * Purchasing Distribution Equipment (you will be assisted by Global group) * Commissioning Distribution Equipment * Commissioning Warehouse Control Systems * Commissioning Facilities, Utilities, HVAC * Client representative and interface with sub-contract companies Requirement for this position are: * Essential that you are fluent in both Dutch and English * Extensive GMP / FDA experience * Cold Chain regulations knowledge * It would be advantageous if you had French language skills too Please apply now for further information on this long term opening that is offering competitive rates of pay. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/commissioning-lead-(dutch-speaking)-europe-j011468 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 12:27:29 GMT http://quantacs.contentedmanagement.co.uk/2876 My client, a global pharmaceutical organisation is building a European Distribution Head Quarters and requires an experienced Qualification Lead for a 12 month contract. This is a Greenfield project and will be focussed on Cold Chain GMP requirements. It is expected that you can lead and drive projects but also be happy to be hands on throughout the project life cycle. You will be responsible for: * Lead all the qualification / validation activities * Be hands on in drafting, writing, executing and reviewing validation documents (URS, Impact Assessments, Protocols etc) * Qualification of Distribution Equipment * Qualification of Warehouse Control Systems * Qualification of Facilities, Utilities, HVAC * Client representative and interface with sub-contract companies for qualification purposes Requirement for this position are: * Essential that you are fluent in both Dutch and English * Extensive GMP / FDA experience * Cold Chain regulations knowledge * It would be advantageous if you had French language skills too Please apply now for further information on this long term opening that is offering competitive rates of pay. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/qualification-lead-(dutch-speaking)-europe-j011469 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 12:27:29 GMT http://quantacs.contentedmanagement.co.uk/2877 A leading European based Biotech organisation involved in an exciting expansion project has a requirement for a Configuration Manager/Database Developer for an initial 6 month contract. As the Configuration Manager working within the automation group you will be responsible for creating and documenting a well structured database for maintain PAS Configuration management information. Skills/Experience required: *Prior experience working within the pharmaceutical industry *Database development experience (MS Access & MS SQL) *Strong database manipulation skills: Able to create and run reports *Demonstrate experience of developing databases and managing conformity *MS package experience *Experience of Completing Configuration Management SOP http://quantacs.contentedmanagement.co.uk/jobs/biotechnology-and-biopharma-jobs/configuration-manager-geneva-switzerland-europe-j011415 Quanta Consultancy Services Ltd Mon, 19 Jul 2010 18:57:32 GMT http://quantacs.contentedmanagement.co.uk/2847 A major Telecoms Vendor requires an OSS Consultant in Radio Network Planning & Optimization / OSS System Designer to work within their OSS R&D Team. This OSS Consulting role provides an opportunity for an experienced OSS RAN Consultant to work as a Business Analyst and work on the System Design within the project that consists of improving and innovating their Radio Network Design & Planning system design tools. The Work will be based in their Swedish based R&D Office. The role and responsibilities: *To be responsible for the E2E business analysis and system Design *To participate in the Radio Network Design & Planning & Optimisation system design *Responsible for the analysis of the Radio Network Planning and optimisation scenario *To take ownership of the analysis of the technology trends within RNO / RNP / RND *Educate & Mentor the System Engineers & Developers Ideal level of experience: *An extremely high amount of experience within Operations in context of the Radio Network Optimisation & planning or Radio Network Design *Experience of using RNO / RNP tools *A high amount of experience of Radio Network feature, optimisation processes and Optimisation parameters. *A good understanding of Radio Network and network maintenance trends *Experience in architecture design for RNO / RNP Tools *Fluent in English *To be eligible to work in Sweden http://quantacs.contentedmanagement.co.uk/jobs/telecoms-jobs/oss-consultant-in-radio-network-planning-sweden-scandinavia-j011461 Quanta Consultancy Services Ltd Mon, 19 Jul 2010 18:57:32 GMT http://quantacs.contentedmanagement.co.uk/2875 European Biotech new build project requires C&Q Technicians to support OQ activities on Automation process equipment. As part of the automation team you will be out in the field performing OQ phase testing within media prep area. Running phases (EM?s and CM?s), writing punches and being involved in deviation management. Skills/experience required: *Pharma production experience in DCS qualification (OQ *Understanding phases (EM?s, CM?s) *Experience with Yokogawa or Delta V systems http://quantacs.contentedmanagement.co.uk/jobs/biotechnology-and-biopharma-jobs/csv-consultant-geneva-switzerland-europe-j011426 Quanta Consultancy Services Ltd Fri, 16 Jul 2010 16:27:28 GMT http://quantacs.contentedmanagement.co.uk/2853 Senior Qualification / Validation Engineer The Engineering Services Department (30 employees) is part of Global Supply Chain. Engineering Services (ES) and is responsible for giving support to all large and complex investment projects. In addition, the department responsible for managing and coordinating all the (project) activities for the qualified to deliver systems and monitoring the quality of those activities. The QV Engineer reports hierarchically and functionally to the manager and operational at the QV project manager of the project where the work to be performed. We are looking for this Senior Qualification/Validation Engineer to work a 6 month contract opportunity in Holland. Responsibilities: - To provide input, advice for the determination of the principles of the project and evaluate them (with the client and / or QA). - Is involved in projects and evaluate projects in terms of qualification and validation. - Does any proposals for such a project to adjust to meet cGMP / cGLP and company policy. - Assesses independently or in a project equipment / systems or qualified to be validated processes and review this with QA. - Assesses ES by others within or outside firms established qualification documents and release these documents may change according to his insights. - Is validation leader of commissioning and validation within projects. Sends in these projects also involved in other fields of knowledge, QC, and CTS, and it is responsible for quality and planning. - Responsible for supervising and checking validation activities performed by third parties. - Maintain contact with QA, QC's, Site Services, Client Representatives, Consultants, Equipment suppliers and manufacturers, inspection authorities, agencies external validation. Job Requirements: - HBO / academic level technical direction (Chemical Engineering) - Experience in the pharmaceutical industry (for Q / V relevant discipline). - Communicative - Good command of English verbal and written (Dutch language knowledge is an advantage) - Good writing skills - Wide-cutting of expertise (technical) knowledge - Experience with inspections is a plus. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/qualification-validation-engineer-eindhoven-holland--europe-j011441 Quanta Consultancy Services Ltd Fri, 16 Jul 2010 08:27:41 GMT http://quantacs.contentedmanagement.co.uk/2865 My client, world leading international pharmaceutical companies are seeking a Regulatory Affairs Scientist for the department of Global Regulatory Affairs- Chemistry Manufacturing & Control (GRA -CMC) in the Netherlands. The CMC department is responsible to carry out all activities that are needed to obtain new registrations and to maintain existing registrations for the projects and products of this manufacturing campus?s portfolio, in particular with respect to chemical/pharmaceutical aspects of the submissions. Tasks and Responsibilities: * Project work encompassing administrative and scientific regulatory activities varying from writing of technical summaries and filling of databases to compliance work, both for pharmaceuticals and/or medical devices. * Draws up CMC documentation for international submissions. * Takes part in the review and release of CMC documents in accordance with the applicable procedures. * Answers questions from health authorities and coordinates the Agency Response process. * Is conversant with relevant, worldwide registration requirements. * Makes proposals to the organization with regard to variations of chemical/pharmaceutical documents following questions from authorities. Consults wit the departments involved. * Has contacts with other MSD staff of local companies and other sister companies. * Sees to planning, coordination and implementation of all the tasks related to his/her project. Requirements: * MSc (Chemistry, Physics, Pharmacy, Analytical Chemistry) or BSc with multiple years of experience. * Minimum of 1 year registration experience in CMC and/or Medical Devices. * Good command of written and spoken English. * Command of Dutch language is an advantage, but not essential. * Good editing skills. * Has good social skills and is a good team player. This is initially a 6 month contract paying competitive rates with possible extensions for a multi-national pharmaceutical organisation. Please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/regulatory-affairs-specialist-holland-europe-j011431 Quanta Consultancy Services Ltd Thu, 15 Jul 2010 16:27:29 GMT http://quantacs.contentedmanagement.co.uk/2857 Quanta?s client, a world leading international pharmaceutical company, are seeking a Regulatory CMC Guideline Specialist / Region Specialist for the department of Network CMC (Chemistry Manufacturing & Control) to be based at their facility in the Netherlands. The Regulatory CMC Guideline Specialist supports the Product Specialists by keeping track of the local regulatory requirements worldwide and update the database with this new information. The Network CMC team is responsible to carry out regulatory activities that are needed in the context of site changes, in particular with respect to chemical/pharmaceutical aspects of the submissions. Tasks and Responsibilities: * The Network CMC point of contact and centre of knowledge with respect to global Health Authority dossier requirements. Advices on filing strategies for Network CMC derived submissions. * Is the centre of knowledge in Network CMC with respect to regulatory requirements and Health Authority expectations for CMC submissions and corresponding submission procedures * Collects Intelligence based on multiple sources (info from local RA representatives, existing and new guidelines, Health Authority responses on earlier submissions) and provides interpretation and practical consequences. * Maintains a regulatory CMC requirements database with key data on dossier content and submission procedures per country/region. Adapts the database as needed, based amongst others on Health Authority feedback and new legislation. * Advices in and outside Network CMC about interpretation of guidelines and provides best practices for dossier content and and submission strategy * Actively supports initiatives on harmonization and standardization of dossiercontent * Supports the Product Specialists by collecting certain dossier elements ( samples, CofA?s, legalized certificates) * Advices Network CMC Planner on official Health Authority review and approval times Requirements: * At minimum a bachelor degree. * Experience in Pharmaceutical CMC or Regulatory Affairs. * Good command of written and spoken English. * Command of Dutch language is an advantage, but not essential * Good editing skills. * Has good social skills and is a good team player. * Able to work on an independent base. The position will start with a 12 months contract, but as the project is expected to be continued, it is very likely that the contract may be extended for a period of about 3 to 4 years. Offering competitive rates and working for a global pharmaceutical organisation this is an opportunity to be taken, please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/regulatory-cmc-guideline-specialist-holland-europe-j011457 Quanta Consultancy Services Ltd Thu, 15 Jul 2010 16:27:29 GMT http://quantacs.contentedmanagement.co.uk/2872 We are currently recruiting for a contract Packaging Engineer for a 9 month position in Ireland. The successful candidate will have experience in the introduction of a new packaging line within a GMP environment. Specific experience of cartoning equipment is required, along with a good understanding of working within regulated environments. This position is due to start in August and will continue for at least nine months. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/packaging-engineer--ireland-eire-europe-j011448 Quanta Consultancy Services Ltd Wed, 14 Jul 2010 12:27:39 GMT http://quantacs.contentedmanagement.co.uk/2867 Senior Project Manager A major Energy Trading company has a requirement for a high level Project Manager. This senior role provides an excellent opportunity for a highly motivated, Project Manager. You will be expected to gain a thorough understanding of a highly complex business area. The role and responsibilities: *To Project Manage and deliver strategic enterprise-wide projects *Planning, estimating and managing work across the full Project life-cycle *Communicate and agree work plans with Senior Management, end-users and technical communities. *Work to defined standards and methods *Demonstrate the ability to lead teams and project work in multi-locations Level of experience required: *Industry experience of Energy or Commodity Trading or Investment Banking as a high level Project Manager *Managing complex, long-term projects within the full trade life cycle *Successful management of application and infrastructure-based projects *Strong stakeholder management skills *Exposure to Front Office, fast-paced Trading environments *Prince2 certified and practitioner *Experience of Trading systems would be advantageous An outstanding daily rate is on offer along side a real opportunity to further your career development within this exciting and expanding global trading company as a Senior Project Manager. Please apply today http://quantacs.contentedmanagement.co.uk/jobs/renewable-energy-and-energy-trading-jobs/project-manager-germany-europe-j011410 Quanta Consultancy Services Ltd Tue, 13 Jul 2010 12:28:55 GMT http://quantacs.contentedmanagement.co.uk/2863