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<item><title><![CDATA[Student Information Systems Manager
	      , Computers/Internet]]></title><link>http://cambridge.ipsojobs.com/job/student-information-systems-manager/3-213361</link><description><![CDATA[<p>The Student Information Systems (SIS) Manager position is responsible for the day-to-day operations, sustainment, maintenance, and growth of MIT&rsquo;s Student Information System (MITSIS). The position reports to the Director of Student and Administrative Systems (SAIS) within the central Information Services and Technology (IS&T) department at MIT. The Student Information Systems Manager will work closely with the other managers and staff within the SAIS directorate area as well as other groups within IS&T. The Manager will also work closely with key leadership in the offices of the Dean of Undergraduate Education, Dean of Student Life, and Dean of Graduate Education to ensure system integrity, availability and quality. &nbsp;The position is a leadership role that represents IS&T to the MIT community and other institutions.</p><br /><p>&nbsp;</p><br /><p>The Manager will engage in strategic initiatives related to Student Information Systems, including strategic planning, budget planning, staff development, and priority setting. The Manager is responsible for defining the agenda, reporting monthly project status, issues and risks to the established Student Systems Steering Committee (SSSC). Likewise, the Manager will be responsible to ensure proper adherence to project management methodologies adopted within IS&T and work to promote and improve these methodologies with the Manager&rsquo;s team as well as within the community which this role serves.&nbsp;&nbsp; The Manager will also be responsible to develop organizational and staff performance measures and metrics.</p><br /><p>&nbsp;</p><br /><p>The Student Information System team consists of the manager plus four team leads, 3 in the key functional support areas of Academic (Registrar), Student Financial Services, and Admissions. The fourth team lead heads the &lsquo;common services&rsquo; team and is responsible for project management on key initiatives and program management including maintenance of documentation standards, audit support, end to end process maps, and the SIS Technology Roadmap.&nbsp; The 14 staff members perform applications analysis and programming, production support, and testing of enhancements and new development.</p><br /><p>&nbsp;</p><br /><p>The primary application supported is a Banner-based legacy system which has been highly customized over the past 15 years, referred to as MITSIS.&nbsp; There is a web component of the system referred to as WEBSIS.&nbsp; The system contains 115 software applications, 5,000 programs covering 100 business functions.&nbsp; Programming languages include JAVA, and Oracle Forms is a key component of the system.&nbsp; The underlying infrastructure is based on Oracle Application Server, WebLogic, and Oracle Database, running on a mix of Solaris and Linux servers.&nbsp; A separate team of system administrators and database administrators reports to the Technical Services manager within SAIS.&nbsp; Close collaboration with the colleague is key to SIS Manager&rsquo;s success.</p><br /><p>&nbsp;</p><br /><p>Candidates for this position should have a minimum of five years of management experience with management of technical teams, application development, project lifecycles, and day-to-day operations.&nbsp;&nbsp; Experience with managing student information systems and custom software development and support in a higher education environment, and PMP or ITIL certification is preferred. The ideal candidate will have a broad understanding of the higher education environment, top-notch communication and team building skills, proven commitment to customer service, and interest in developing solid partnerships with the Institute community including but not limited to the Office of Undergraduate Education, Office of Dean of Student Life, and the Office of the Dean for Graduate Education.&nbsp;&nbsp;</p><br /><p>&nbsp;</p><br /><p>Duties of the Manager may include, but are not limited to--</p><br /><ul><br /><li>Team Management    <br /><ul><br /><li>Lead a team of approximately 20 technical staff in the delivery of uninterrupted services to the core system of MIT &ndash; the Student Information System</li><br /><li>Ensure best use of resources in line with the needs of the business community</li><br /><li>Build a strong relationship with team leads and team members</li><br /></ul><br /></li><br /><li>Business relationships&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;     <br /><ul><br /><li>Build strong positive and trusting relationships with leadership in the Office of the Dean of Undergraduate Education, the Office of Dean for Student Life, and the Office of the Dean of Graduate Education</li><br /><li>Ensure open communication on issues within this environment</li><br /><li>Learn and understand the business culture, processes, requirements and constraints of the business community,.</li><br /></ul><br /></li><br /><li>Production Release Control     <br /><ul><br /><li>&nbsp;ensure proper adherence to Quality Control, approve or delegate approval of transports, train staff in areas of production release control</li><br /></ul><br /></li><br /><li>Ensuring proper project methodology    <br /><ul><br /><li>ensure proper adherence to adopted project management methodology,&nbsp; ensure project plan, risks, issues and budget are on track and communicate to Director in event project is in risk,&nbsp; identify and train staff in areas of project management methodology</li><br /></ul><br /></li><br /><li>Remove project barriers    <br /><ul><br /><li>Responsible for ensuring project delivery and identifying and remediating project barriers, either independently or with support of Director</li><br /></ul><br /></li><br /><li>Ensure adherence to department standards    <br /><ul><br /><li>Ensure that programmers follow the set standards of the architect for SIS.&nbsp; Encourage technical staff to participate and evolve our standards and procedures.</li><br /></ul><br /></li><br /><li>Staff management/development    <br /><ul><br /><li>Understand needs of the business customer and organize team appropriately.&nbsp; Request resources as necessary.&nbsp; Identify gaps in staff skills and train/hire appropriately.&nbsp; Confidently take action on Employment Relations issues in partnership with HR.</li><br /></ul><br /></li><br /><li>Collaborate with NGS3 Team    <br /><ul><br /><li>Work closely with the Next Generation Student Services Program to ensure alignment and sharing of knowledge and work plans,&nbsp; to keep staff informed, and to have input how best to use all Student Information Services resources in the best interest of MIT.</li><br /></ul><br /></li><br /><li>Report metrics     <br /><ul><br /><li>In conjunction with Director and colleagues, define and report quarterly metrics on system availability, system changes, and project status</li><br /></ul><br /></li><br /><li>Leadership Working Group    <br /><ul><br /><li>Actively participate in the Leadership Working Group to support IS&T in the advancement of its mission and goals.</li><br /></ul><br /></li><br /><li>Budget prep and monthly reconciliation    <br /><ul><br /><li>Work in partnership with the Finance Team to develop the budget, define project budgets and track and confirm actual expenditures.&nbsp; Be proactive in communicating to Finance any changes or anticipated changes or requests in projects or work.</li><br /></ul><br /></li><br /></ul><br /><p>&nbsp;</p><br /><p>&nbsp;</p><br /><p>&nbsp;</p><br /><br /><br /><strong>Industry:</strong> Education<br /><strong>Discipline:</strong> IT Mngmnt and Project Mngmnt<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Compensation:</strong> $125K+<br /><strong>Company:</strong> Massachusetts Institute of Technology]]></description><pubDate>Sun, 08 Nov 2009 23:16:23 -0800</pubDate></item><item><title><![CDATA[Senior Web Engineer
	      , Computers/Internet]]></title><link>http://cambridge.ipsojobs.com/job/senior-web-engineer/3-213345</link><description><![CDATA[<p>Our client runs one of the world&rsquo;s largest social networking sites.&nbsp; Based in Cambridge, MA, they offer employees the opportunity to work on some of the most innovative technology platforms and the chance to help solve real business issues.&nbsp; Under the leadership of a new CTO, their technology team is expanding and we&rsquo;re helping them add to an already impressive team.</p><br /><p>&nbsp;</p><br /><p>The Senior Web Engineer is responsible for the development, implementation, and maintenance of applications including development methods and standards. The main function of the Senior Web Engineer is to assist in the development of applications and systems using PHP, Symfony, Memcached, and MySQL.</p><br /><p>&nbsp;</p><br /><p>Looking for candidates who have</p><br /><ul><br /><li>At least 5 years experience with PHP</li><br /><li>Large scale applications (greater than 1 million users)</li><br /><li>Experience with developing and maintaining highly available or fault-tolerant software systems across the full application lifecycle</li><br /><li>Extensive knowledge of PHP, MySQL, Linux, and Apache</li><br /><li>Extensive experience in a Unix environment</li><br /><li>Extensive experience with MySQL database architecture and design</li><br /></ul><br /><br /><br /><strong>Industry:</strong> Internet Services<br /><strong>Discipline:</strong> SW Design/Dev<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Compensation:</strong> $115K<br /><strong>Company:</strong> Premier social networking company]]></description><pubDate>Sun, 08 Nov 2009 23:16:22 -0800</pubDate></item><item><title><![CDATA[Accounting Manager - Public Pharmaceutical
	      , Accounting/Finance]]></title><link>http://cambridge.ipsojobs.com/job/accounting-manager-public-pharmaceutical/18-213279</link><description><![CDATA[<strong>About the company :<br />Our client is a growing, publicly traded Biotech with secured funding platform until 2013..<strong> Job description :<br />An exciting opportunity to join a growing publicly traded biotech in Cambridge. Reporting to the Assistant Controller, the Accounting Manager will be an enthusiastic, strong leader with a solid technical accounting background. The Accounting Manager will be a front-line general ledger manager at a public company.Primary responsibilities include:  Managing the accounting and reporting function consisting of the monthly closing and consolidation process, general ledger, cash receipts/disbursements and shared-based compensation (including SFAS 123R - using Equity Edge).   Ensuring that the close process is streamlined; roles and responsibilities of those involved are appropriate and implement any changes necessary to improve the process.  Creating the majority the of businesss internal financial reports  Lead the creation of all the external reports including SEC Form 10-Qs, and 10-K  Assist in the development of any other SEC reports, as well as, the Annual Report to Shareholders, Audit Committee and BOD Financial Statements  Manager detailed schedules for business collaborations  Lead the coordination and support of the independent auditors in their quarterly reviews and annual audits  Prepare technical accounting memos when needed  Maintain and ensure ongoing compliance with accounting policies and procedures and Sarbanes-Oxley Act (SOX) internal control documentation.  Review journal entries, balance sheet reconciliations / reviews and internal control work  Lead other specific projects and/or initiatives as required  Potentially manage 1-2 members of the finance team<strong> Who we are looking for   :<br />The Accounting Manager will offer:  CPA, Big 4 or large regional CPA firm a must  Experience working with a LifeSciences business a plus  Experience also working in a Industry setting strongly preferred  SEC Reporting experience essential  Strong Management skills required.<strong> Whats on offer  :<br />The Accounting Manager will be offered a competitive base salary to $120k + bonus + strong benefits.</strong></strong></strong></strong><br /><br /><br /><strong>Industry:</strong> Biotech/Pharma<br /><strong>Discipline:</strong> Accounting & Controls<br /><strong>Compensation:</strong> $100K - $120K<br /><strong>Company:</strong> Pharmaceuticals Company]]></description><pubDate>Sun, 08 Nov 2009 23:16:04 -0800</pubDate></item><item><title><![CDATA[Scientist (Analytical Chemistry) - NB50919718
	      , Medical/Health]]></title><link>http://cambridge.ipsojobs.com/job/scientist-analytical-chemistry-nb50919718/9-209857</link><description><![CDATA[Basic Qualifications: Masters degree in analytical chemistry, chemistry, pharmaceutical sciences, biochemistry, or related chemistry field with 5+ years industry experience Experience in any of the following: wet chemistry, separation/spectroscopic sciences and associated instrumentation and synthetic organic chemistry or formulation development Preferred Qualifications: Ph.D. degree in analytical chemistry, chemistry, pharmaceutical sciences, biochemistry, or related chemistry field Research in and hands-on experience with mass spectrometry, solid state characterization, or process analytical technologies (PAT) and data analysis (e.g. chemometrics) packages Familiarity with process/chemical engineering for the manufacturing of small molecule drug substances and products Excellent written and oral communication skills are required for the timely documentation, presentation, and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment Strong abilities in trouble-shooting, problem-solving, data review and interpretation, and multi-tasking  Amgen Inc. in Cambridge, MA is seeking an outstanding scientist to contribute to the scientific development of small molecule drug substance and drug product processes. This primarily laboratory-based position offers the ability to apply, invent and continue learning fundamental and cutting-edge analytical chemistry in a cross-functional team environment. Key responsibilities for this position include the development and execution of on- and off-line chromatographic, spectroscopic, and solid-state methods to monitor and understand process development from initial route screening to pilot and factory scale manufacturing.<br /><br /><br /><strong>Industry:</strong> Biotech/Pharma<br /><strong>Discipline:</strong> Biotech, Pharma, Med. Device R&D<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Compensation:</strong> $100K+<br /><strong>Company:</strong> Amgen Inc]]></description><pubDate>Sun, 01 Nov 2009 23:16:11 -0800</pubDate></item><item><title><![CDATA[COO- Operations & Technology Manager-Financial Services
	      , Sales/Marketing]]></title><link>http://cambridge.ipsojobs.com/job/coo-operations-technology-manager-financial-services/12-207660</link><description><![CDATA[<p>Leading alternative asset manager with a range of institutional and private clients operating in Europe, the United States and Asia Pacific. With established offices in Chicago and New York, they are now looking to build upon their Boston office. Our client specializes in managing equities, commodities & currencies. The firm employs a quantitative style of managing portfolios. <br /> <br /> Manage all operational aspects for the US, including the following:<br /> <br /> Operations and Technology<br /> &bull; Manage relationships with systems administrators, technology vendors, telecom<br /> &bull; Manage evaluations of providers of trading, accounting, risk management, valuation systems versus &lsquo;build it ourselves&rsquo;<br /> &bull; Business continuity plan<br /> &bull; Real estate and office<br /> <br /> Fund operations<br /> &bull; Daily NAV, performance attribution, reconciliation, trade errors, settlement<br /> &bull; Fund cash management<br /> &bull; Monthly reporting to clients<br /> &bull; Margin reports, counterparty reports<br /> &bull; Manage relationship with brokers, administrator, auditor <br /> &bull; Fund audit<br /> <br /> Fund infrastructure<br /> &bull; Cayman, Luxembourg structures, US feeders<br /> &bull; Legal<br /> <br /> Prime brokerage<br /> &bull; Dealer credit relationship<br /> &bull; Control, monitor dealer credit<br /> <br /> Finance<br /> &bull; Budgeting <br /> &bull; Coordinate finance with head office<br /> &bull; Company Audit<br /> <br /> Compliance<br /> &bull; Establish procedures, compliance manual for institutional level due diligence<br /> &bull; Internal control manual<br /> &bull; Regulators (SEC, Cayman&hellip;), ADV<br /> <br /> HR<br /> &bull; Coordinate payroll, benefits etc. with head office<br /> &bull; Lead collecting and screening of resumes, work with recruiters<br /> <br /></p><br /><br /><br /><strong>Industry:</strong> Financial Services<br /><strong>Discipline:</strong> Bus Dev<br /><strong>Experience:</strong> 8 - 10 Years<br /><strong>Level:</strong> Manager<br /><strong>Compensation:</strong> $200K<br /><strong>Company:</strong> Top Asset Managment Firm]]></description><pubDate>Sun, 25 Oct 2009 23:08:12 -0700</pubDate></item><item><title><![CDATA[Director of Regulatory Affairs BHJOB1778_219
	      , Medical/Health]]></title><link>http://cambridge.ipsojobs.com/job/director-of-regulatory-affairs-bhjob1778-219/9-206177</link><description><![CDATA[<p>The Wellington Group is seeking an experienced regulatory affairs professional for an exciting new medical device / combination therapy position. Excellent opportunity to help bring new medical devices to the global market! <br /><br />The Director of Regulatory Affairs is a key role in the development, research and commercialization of new products and the management of regulatory and quality disciplines for the organization. The Director will ensure that the company complies with applicable global regulatory requirements and standards for the development, pre-clinical and clinical evaluation, manufacturing, and marketing of its products. <br /><br />Responsibilities include: <br />&bull; Lead a team of regulatory professionals to define and implement the regulatory strategy <br />&bull; Lead the preparation, submission, and timely approval of regulatory applications <br />&bull; Lead the interaction and negotiations with regulatory agencies <br />&bull; Maintain regulatory procedures and documents to maintain approvals and certification for development, manufacturing, and marketing of products <br />&bull; Inform senior management of regulatory requirements and status of products and significant regulatory issues/trends <br /><br />The qualified candidate will have: <br />&bull; 10+ years of Regulatory Affairs experience with at least 4 years of medical devices and 4 years in senior manager <br />&bull; 4-year degree required, graduated degree preferred <br />&bull; Experience in providing regulatory direction to development, pre-clinical and clinical evaluation, manufacturing, and marketing of combination products <br />&bull; Experience in preparing and obtaining approval of device/drug combination products <br />&bull; FDA/ISO/CE submissions and follow-up maintenance activities for approvals and certifications <br />&bull; Significant experience planning for and management of regulatory compliance audits <br /><br />Industry: Medical Devices, Biologics, Pharmaceutical <br /><br />Location: Either RTP, NC or Cambridge, MA <br /><br />Permanent position with an employee centered company offering great benefits, salary, bonus and relocation assistance. <br /><br />Don&rsquo;t wait, apply with The Wellington Group today! <br />(all information will be held in the strictest of confidence) <br /><br />The Wellington Group</p><br /><br /><br /><strong>Industry:</strong> Medical Devices & Diagnostics<br /><strong>Discipline:</strong> Biotech, Pharma, Med. Device R&D<br /><strong>Experience:</strong> 11 - 15 Years<br /><strong>Level:</strong> Director<br /><strong>Compensation:</strong> $140K+<br /><strong>Company:</strong> Medical Devices & Diagnostics Company]]></description><pubDate>Sun, 18 Oct 2009 23:13:45 -0700</pubDate></item><item><title><![CDATA[Director of Clinical Research BHJOB1778_220
	      , Medical/Health]]></title><link>http://cambridge.ipsojobs.com/job/director-of-clinical-research-bhjob1778-220/9-205975</link><description><![CDATA[<p>The Wellington Group is seeking an experienced Clinical Operations professional for an exciting new medical device / combination therapy position. Excellent opportunity to help bring new medical devices to the global market through developing a quality clinical program! <br /><br />The Director of Clinical Affairs is a key management position in the development, research and commercialization of new products. The Director will develop, implement and manage the company&rsquo;s clinical research strategy. <br /><br />Responsibilities include: <br />&bull; Design and direct the company&rsquo;s global clinical study strategy to obtain timely regulatory approval of products and acceptance by clinicians <br />&bull; Lead the design of credible clinical studies, integrating inputs from clinical study professionals, clinicians, statisticians, regulatory agencies, and management <br />&bull; Manage contracted Clinical Research and Core Lab staff and other consultants to prepare materials, engage clinicians, conduct studies, compile data, and produce reports on schedule and within budgets <br />&bull; Develop relationships with participating clinicians and clinical research staff to assure effective management and communications <br />&bull; Lead the preparation of the clinical portion of regulatory submissions <br />&bull; Represent the company&rsquo;s clinical perspective in regulatory agency interactions <br />&bull; Inform senior management of clinical study status and issues <br />&bull; Participate in publication of clinical results <br /><br />The qualified candidate will have: <br />&bull; 10+ years working in clinical study programs in the medical products industry, including at least 4 years managing design and successful completion of clinical studies for device/drug combination products <br />&bull; Demonstrated effectiveness in managing and motivating Clinical Research Organizations <br />&bull; Significant role in directing participating clinicians <br />&bull; Knowledge of international clinical regulatory requirements <br />&bull; Strong planning, communication, and management skills <br />&bull; Preparation of clinical publications <br />&bull; BS/MS in life sciences with training in clinical research <br />&bull; Frequent international travel <br /><br />Industry: Medical Devices, Biologics, Pharmaceutical <br /><br />Location: Either RTP, NC or Cambridge, MA <br /><br />Permanent position with an employee centered company offering great benefits, salary, bonus and relocation assistance. <br /><br />Don&rsquo;t wait, apply with The Wellington Group today! <br />(all information will be held in the strictest of confidence)</p><br /><br /><br /><strong>Industry:</strong> Medical Devices & Diagnostics<br /><strong>Discipline:</strong> Biotech, Pharma, Med. Device R&D<br /><strong>Experience:</strong> 11 - 15 Years<br /><strong>Level:</strong> Director<br /><strong>Compensation:</strong> $100K+<br /><strong>Company:</strong> Medical Devices & Diagnostics Company]]></description><pubDate>Sun, 18 Oct 2009 23:10:06 -0700</pubDate></item><item><title><![CDATA[Sr. Software Development Engineer - Research - 256573
	      , Computers/Internet]]></title><link>http://cambridge.ipsojobs.com/job/sr-software-development-engineer-research-256573/3-205944</link><description><![CDATA[Do you have a passion to build innovative tools and services  Do you want to work in a research lab on state of the art projects  Are you curious about interdisciplinary research that brings together computer scientists and social scientists  <br /><br />Located in Cambridge, Massachusetts, Microsoft Research New England is building on Microsoft&rsquo;s commitment to advance the state of the art in multiple areas of computing research. The lab, Microsoft Research&rsquo;s sixth research facility worldwide, is pursuing new, interdisciplinary areas of research that bring together core computer scientists and social scientists to understand, model, and enable the computing online experiences of the future. <br /><br />We are looking for a software developer who will be a member of the research lab working on projects that may be in any stage of development. As part of an engineering team you will work with researchers, program managers and designers to implement new concepts into prototypes, research tools and services. We are looking for someone who has a passion for developing and delivering product quality code while working in a dynamic research environment. <br /><br />You will be responsible for executing all phases of development on new projects. You will scope deliverables and participate in writing requirements and design specs. Your primary work will involve programming, including prototyping, product quality coding, automated unit and regression testing, and debugging. <br /><br />Qualified candidates will have 5-8 years of software development experience, including testing and deploying iterative releases of software systems. Candidates must be adept at working with MSR researchers to translate their ideas into production-ready code. Strong theory/algorithms background and exceptional problem solving and analytical skills are a must. Experience developing commercial software using C# / .NET and C++ development experiences with expert knowledge of Windows programming is required. All candidates must have outstanding communication skills, and be capable of establishing and maintaining relationships with all levels and roles within Microsoft New England Research and Development Center.<br /><br /><br /><strong>Industry:</strong> Software<br /><strong>Discipline:</strong> SW Design/Dev<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Compensation:</strong> $100K+<br /><strong>Company:</strong> Microsoft Corporation]]></description><pubDate>Sun, 18 Oct 2009 23:09:30 -0700</pubDate></item><item><title><![CDATA[Fiber - Optic Engineer  /  Scientist - ST / 078013
	      , Computers/Internet]]></title><link>http://cambridge.ipsojobs.com/job/fiber-optic-engineer-scientist-st-078013/3-189028</link><description><![CDATA[Defining the future. Join the men and women of Northrop Grumman Aerospace Systems in meeting the largest, most complex systems challenges imaginable for government, military and business. Job Title: Fiberoptic Engineer/Scientist Job ID # 78013 Job Description: Perform as member of interdisciplinary team of scientists and engineers on different project assignments focused on the design, modeling, test, and transfer to manufacturing of fiberoptic components and subsystems. Support laboratory product integration as well as development of hardware for fiberoptic communication systems. Design methods and techniques for components and system testing of high-speed digital and optical modules and subsystems. Develop mathematical models for performance analysis. Support proposal teams and work with customers on product definition. Complete tasks according to schedule, budget, cost and design objectives. Basic Qualifications: BS in Physics, Optics, or Electrical Engineering. 5+ years experience in fiberoptic system/component engineering. Thorough understanding and experience with fiber optics components, such as diode lasers, external modulators, various fibers types, couplers, isolators, WDMs, tunable filters, EDFAs, dispersion compensators, fiber switches, receivers etc. Experience in the fundamentals of F/O subsystems assembly, including fiber pig-tailing, splicing, connectorization, and optical packaging. Demonstrate understanding of fiber-optic transmission and digital communication theory. Knowledge of high-speed optoelectronic test equipment for SONET and Ethernet optical modules is advantageous. U.S. citizenship required. Must possess or be able to obtain a Top Secret security clearance. Assets (Preferred, not needed): Current TS/SCI security clearance MS or PhD a plus <br /><br /><br /><strong>Industry:</strong> Aerospace / Defense<br /><strong>Discipline:</strong> Electrical/Electronic Engin.<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Compensation:</strong> $100K+<br /><strong>Company:</strong> Northrop Grumman]]></description><pubDate>Sun, 13 Sep 2009 23:19:43 -0700</pubDate></item><item><title><![CDATA[Manager, Industrial Security - ST /  089868
	      , Computers/Internet]]></title><link>http://cambridge.ipsojobs.com/job/manager-industrial-security-st-089868/3-188707</link><description><![CDATA[Defining the future. Join the men and women of Northrop Grumman Aerospace Systems in meeting the largest, most complex systems challenges imaginable for government, military and business. Job Title: Manager of Industrial Security & IT Job ID:89868 Job Description: Responsible for department of three individuals providing Security support to multiple locations. Will operate as Facility Security Officer (FSO). Develops, and administers security programs and procedures for classified or proprietary materials, documents, and equipment. Studies and implements federal security regulations that apply to company operations. Obtains rulings, interpretations, and acceptable deviations for compliance with regulations from government agencies. Prepares manuals outlining regulations, and establishes procedures for handling, storing, and keeping records, and for granting personnel and visitors access to restricted records and materials. Conducts security education classes and security audits. Investigates security violations and prepares reports specifying preventive action to be taken. Additionally, responsible for day to day oversight of secure operating systems and networks. Invovled in a wide range of security issues including arhcitectures, firewalls, electronics data traffic, and network access. Uses cryption technology, penetration and vulnerability analysis of various security technologies. Basic Qualifications: B.A. or B.S. degree in related field A minimum of 6 years experience in Security field; minimum 3 years in Information Technology Knowledge and experience with the NISPOM Must be self-directed, dependable, detail-oriented and able to multi-task. Excellent organizational skills and oral/written communication skills are necessary. TS (Top Secret) clearance required Assets (Preferred qualifications): CISSP certification FSO experience<br /><br /><br /><strong>Industry:</strong> Aerospace / Defense<br /><strong>Discipline:</strong> Networks & Systems<br /><strong>Experience:</strong> 5 - 7 Years<br /><strong>Level:</strong> Manager<br /><strong>Compensation:</strong> $100K+<br /><strong>Company:</strong> Northrop Grumman]]></description><pubDate>Sun, 13 Sep 2009 23:18:06 -0700</pubDate></item>

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