http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-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 key client of Quanta, a leading vaccine manufacture is seeking a Transportation Specialist to join their Customer Response and Distribution Team. This position will be based at their parent organisation?s central headquarters in Switzerland. Responsibilities will include: * The role holder must ensure all staff associated with shipping product to customers are trained to be competent to deliver their activities, and that there is sufficient capacity for the budgeted distribution work. * Ensuring the Distribution staff at all sites provides current and accurate data for ERP system (and its associated sub-systems e.g. SAP BW.) as required by agreed global and site data management processes. * Ensure cold chain and complex customer warehouse requirements are understood and solutions delivered. Work closely with Quality function for cold chain and transportation SOPs and compliance. * Evaluate cost control opportunities in all areas of transportation and warehousing, as part of the order delivery process to customers. * This is a global role and it is expected a significant proportion of time will be spent sharing standard procedures, training and auditing around manufacturing sites, third party distribution networks and customer receiving-warehouses. * Although having no direct staff responsibilities for Distribution activities at sites, the role holder will provide functional guidance on all transportation matters, including problem-solving for distribution risks and issues, and looking for continuous improvement opportunities. * High travel requirement (up to 75% globally) Education (minimum/desirable): * A degree in Scientific; Engineering or Commercial discipline; if Commercial, then additional industrial experience of supply chain management (logistics / shipping / cold chain). * Languages: English (fluent) and ideally German, French or Italian. Relevant Experiences: * Knowledge and experience of distribution / transportation / shipping. * Knowledge of cold chain requirements, including containers and temperature monitors. * Interpersonal, motivational and training skills ? an ability to influence across all levels and between Commercial regions in the organisation. * First class communication abilities; the role will provide information through presentations at every level of the company. * Experience working within cross-functional teams. * Experience in multicultural and matrix environments. * Demonstrated leadership of change and improvement projects. This is a fantastic opportunity to work with a forward thinking team, offering a great remuneration package and with great professional development chances. Please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/transportation-specialist-(cold-chain)-europe-j011485 Quanta Consultancy Services Ltd Mon, 26 Jul 2010 18:57:28 GMT http://quantacs.contentedmanagement.co.uk/2889 A new permanent opportunity has arisen with a rapidly growing Biopharmaceutical organisation. They require a Senior QA Officer (Auditor) to join their UK headquarters on the Cambridgeshire / Suffolk border. The main purpose of the role will be to maintain and manage cGMP quality systems for the site, including support of implementation of corporate Quality Management System. Assists with administrative support for TrackWise workflows. Provides back-up for internal and supplier audits. Key Responsibilities: * Work with Site Administrator to provide administrative support and training for on-site TrackWise users for all workflows * Provide back-up support for off-site interactions regarding TrackWise * Perform internal audits and external audit / inspections of suppliers of goods and services, included computerised systems as required * Support implementation of corporate QMS system, including communication with site, support of process owners with regard to gap analysis, gap closure and update of SOPs * Develop and maintain metrics for monitoring performance of the site QMS, as required * Support communication of compliance status to site Knowledge, Skills and Experience Required: * Typically a graduate or equivalent, and may be working towards externally accredited qualifications * Demonstrated knowledge of working within a quality management system, including thorough knowledge of cGMP * Demonstrated ability to facilitate/perform quality audits successfully * Ideally have Lead Auditor qualification This is a fantastic time to join this evolving biotech organisation and work in a exciting work environment with great career growth opportunities. Please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/senior-qa-auditor-(compliance)-east-anglia-uk-j011475 Quanta Consultancy Services Ltd Tue, 20 Jul 2010 16:27:29 GMT http://quantacs.contentedmanagement.co.uk/2885 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 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 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 Senior Quality Director is required to join one of the world's foremost biotechnology companies based in Suffolk. The purpose of this opportunity will be to manage the quality department and its relationships both on-site and beyond so that it runs efficiently and effectively. At all times the Senior Quality Director will use their best practices knowledge and the most cost effective methods available to ensure that the site operation, as a minimum, complies to the appropriate quality standards. The Senior Quality Director will also ensure that the business delights its customer and is recognised as a best in class, high performance organisation . The position will require you to report directly to the VP and GM of Operations and the Senior VP or Quality & Technical Operations. Key Responsibilities *Be part of the Senior Management Team developing and managing business strategies designed to place the business in a highly competitive position in line with its strategy and objectives *Network and communicate widely and be highly influential in order to persuade others to see us in an exceptionally positive way and to give appropriate consideration to our stance on the issues that impact our business. *Ensure that the Quality function is adequately resourced to ensure that it can discharge its responsibilities under UK/EU medicines legislation and GMP guidance?s and the relevant legislation/guidance?s of other countries where the client products may be sold or supplied.. *Leads the Quality team, which consists of various QC, QCTS, QA (including QP's) site regulatory affairs and Validation personnel, to excellent and consistent performance through inspiring and visible leadership. Provides direction, coaching and advise to the Quality management staff to achieve goals related to HH supported initiatives while keeping the cost of quality in line with or better than best in class. *Ensure that the quality function maintains a broad knowledge of upcoming and current industry best practices and regulatory requirements and proactively maintains relationships so that the business consistently has a position where internal and external auditors such as the Corporate Audit group, FDA, MHRA, other country Regulatory Agencies and all customers see us as operating with a high degree of Compliance with the relevant regulations, policies and guidance?s and provide product of consistent quality in compliance with all of the relevant regulatory filings *Work as an integral and fundamental part of the Corporate Quality organisation so that the business influencing, aligned with and taking a leadership role in appropriate quality initiatives. *Develop and manage quality systems that ensure that site management, internal departmental function, other client manufacturing sites, contract manufacturers and laboratories, suppliers, Regulatory affairs and Global Quality management to deliver compliant reliable cost effective and timely supply of client products for release to worldwide markets. *Manages the quality process on site so that it is an integral part of the way all departments work by encouraging and facilitating interdepartmental collaboration and the participation of quality interdepartmental activities. The position of Senior Quality Director will not directly supervised other than for setting and achieving objectives. The candidate will be expected to sets objectives for themselves and define methods and measures to be used. This Senior Quality Directors post will require the person to be professionally qualified and will have substantial experience of successfully working at a senior level and be able to demonstrate a broad and deep technical/managerial understanding. They will have managed others successfully and have an advanced grasp of management techniques and be a high quality role model. Please do apply for more details. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/senior-quality-director-east-anglia-uk-j011450 Quanta Consultancy Services Ltd Wed, 14 Jul 2010 18:57:33 GMT http://quantacs.contentedmanagement.co.uk/2869 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 Junior Project Engineer required by leading independent pharmaceutical manufacturing company specialising in healthcare products Due to continuing success, the need to expand their Project Engineering team has arisen. As the Junior Project Engineer you will be required to manage a variety of projects across engineering, systems and facilities disciplines and these projects could range from, civil based works or overseeing the installation of filling lines through to the relocation of existing machinery. Background required: This Junior Graduate position requires applicants with a right to work in the UK, and previous work experience within a relevant industry such as pharmaceutical/medical devices/automotive or food & drink. Person specification: *Degree qualified in an Engineering related discipline * Knowledge of manufacturing equipment such as packaging equipment and manufacturing systems. *Experience of civil based projects *Highly PC Literate *An understanding of the theories of GMP *Knowledge of Lean Manufacturing methodologies This is an exciting first opportunity to join a successful pharmaceutical company enjoying continuing success and expansion. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/project-engineer-north-east-uk-j011418 Quanta Consultancy Services Ltd Fri, 25 Jun 2010 12:27:37 GMT http://quantacs.contentedmanagement.co.uk/2848 A client in the Middle East requires a team of automation / instrumentation individuals to ensure they deliver their project in a 2 year timescale. We require the following individuals for the project: 1) Lead Engineer DeltaV & Ovation 2) Field Service Engineer for DeltaV and Ovation 3) Measurement Instrumentation Engineer for Pressure, temperature, level and flow instrumentation consisting of Rosemount and Micro Motion product range 4) Control Valves Support Engineer for Fisher Control Valves 5) Rosemount Analytical Gas and Liquid Analyzers & Gas Chromatographs Metering Skid Support Engineer for Daniel flow metering skids consisting of DP based flow meters, Ultrasonic flow meters, Flow computers and HMI 6) SCADA Engineer for Bristol system The duration of the contract would be approx. 2 years and you will be working on a rotation basis of 4 weeks (so 4 weeks on-site, 4 weeks off-site). This project is offering excellent rates of pay; brilliant expenses so please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/field-service-engineer---delta-v-middleeast-j011395 Quanta Consultancy Services Ltd Wed, 16 Jun 2010 16:27:40 GMT http://quantacs.contentedmanagement.co.uk/2834 A client in the Middle East requires a team of automation / instrumentation individuals to ensure they deliver their project in a 2 year timescale. We require the following individuals for the project: 1) Lead Engineer DeltaV & Ovation 2) Field Service Engineer for DeltaV and Ovation 3) Measurement Instrumentation Engineer for Pressure, temperature, level and flow instrumentation consisting of Rosemount and Micro Motion product range 4) Control Valves Support Engineer for Fisher Control Valves 5) Rosemount Analytical Gas and Liquid Analyzers & Gas Chromatographs Metering Skid Support Engineer for Daniel flow metering skids consisting of DP based flow meters, Ultrasonic flow meters, Flow computers and HMI 6) SCADA Engineer for Bristol system The duration of the contract would be approx. 2 years and you will be working on a rotation basis of 4 weeks (so 4 weeks on-site, 4 weeks off-site). This project is offering excellent rates of pay; brilliant expenses so please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/measurement-instrument-engineer-middleeast-j011396 Quanta Consultancy Services Ltd Wed, 16 Jun 2010 16:27:40 GMT http://quantacs.contentedmanagement.co.uk/2835 A client in the Middle East requires a team of automation / instrumentation individuals to ensure they deliver their project in a 2 year timescale. We require the following individuals for the project: 1) Lead Engineer DeltaV & Ovation 2) Field Service Engineer for DeltaV and Ovation 3) Measurement Instrumentation Engineer for Pressure, temperature, level and flow instrumentation consisting of Rosemount and Micro Motion product range 4) Control Valves Support Engineer for Fisher Control Valves 5) Rosemount Analytical Gas and Liquid Analyzers & Gas Chromatographs Metering Skid Support Engineer for Daniel flow metering skids consisting of DP based flow meters, Ultrasonic flow meters, Flow computers and HMI 6) SCADA Engineer for Bristol system The duration of the contract would be approx. 2 years and you will be working on a rotation basis of 4 weeks (so 4 weeks on-site, 4 weeks off-site). This project is offering excellent rates of pay; brilliant expenses so please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/control-valves-support-engineer-middleeast-j011397 Quanta Consultancy Services Ltd Wed, 16 Jun 2010 16:27:40 GMT http://quantacs.contentedmanagement.co.uk/2836 A client in the Middle East requires a team of automation / instrumentation individuals to ensure they deliver their project in a 2 year timescale. We require the following individuals for the project: 1) Lead Engineer DeltaV & Ovation 2) Field Service Engineer for DeltaV and Ovation 3) Measurement Instrumentation Engineer for Pressure, temperature, level and flow instrumentation consisting of Rosemount and Micro Motion product range 4) Control Valves Support Engineer for Fisher Control Valves 5) Rosemount Analytical Gas and Liquid Analyzers & Gas Chromatographs Metering Skid Support Engineer for Daniel flow metering skids consisting of DP based flow meters, Ultrasonic flow meters, Flow computers and HMI 6) SCADA Engineer for Bristol system The duration of the contract would be approx. 2 years and you will be working on a rotation basis of 4 weeks (so 4 weeks on-site, 4 weeks off-site). This project is offering excellent rates of pay; brilliant expenses so please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/rosemount-skid-support-engineer-middleeast-j011398 Quanta Consultancy Services Ltd Wed, 16 Jun 2010 16:27:40 GMT http://quantacs.contentedmanagement.co.uk/2837 A client in the Middle East requires a team of automation / instrumentation individuals to ensure they deliver their project in a 2 year timescale. We require the following individuals for the project: 1) Lead Engineer DeltaV & Ovation 2) Field Service Engineer for DeltaV and Ovation 3) Measurement Instrumentation Engineer for Pressure, temperature, level and flow instrumentation consisting of Rosemount and Micro Motion product range 4) Control Valves Support Engineer for Fisher Control Valves 5) Rosemount Analytical Gas and Liquid Analyzers & Gas Chromatographs Metering Skid Support Engineer for Daniel flow metering skids consisting of DP based flow meters, Ultrasonic flow meters, Flow computers and HMI 6) SCADA Engineer for Bristol system The duration of the contract would be approx. 2 years and you will be working on a rotation basis of 4 weeks (so 4 weeks on-site, 4 weeks off-site). This project is offering excellent rates of pay; brilliant expenses so please apply now for more information. http://quantacs.contentedmanagement.co.uk/jobs/pharmaceuticals-jobs/scada-engineer---bristol-middleeast-j011399 Quanta Consultancy Services Ltd Wed, 16 Jun 2010 16:27:40 GMT http://quantacs.contentedmanagement.co.uk/2838