Engineer Jobs in New Jersey

Job Title: RF/MICROWAVE ENGINEER - PRINCIPAL MEMBER TECHICAL STAFF Company: ITT Defense Electronics & Services Location: Clifton, NJ Description: ITT is a global engineering and manufacturing company with $11.7 billion in sales. Thanks to our talented employees, we develop applications that meet our customers'' exacting requirements and tackle some of the world''s most complex problems. This is an exciting opportunity to join an international leader in the design, production and support of Electronic warfare protection systems. We develop technology critical to our soldiers and you have the potential to become part of a talented team, work on rewarding projects, thrive in a dynamic environment and excel in your career. As a Lead Engineer working on the RF/Microwave Design Engineering Team, you will have the opportunity to investigate and develop new advances being used in high performance RF and Microwave Assemblies and Sub-assemblies. Must have the ability to work with minimal supervision, be a self-starter, work well in a team environment, and follow established policies and procedures. In this role, you will be responsible for the design and development of complex Microwave Assemblies and Multi Chip Assemblies. A high degree of care and attention to detail is required in the performance of duties to minimize any substantial and serious impacts to projects. There may be an opportunity to organize and perform special assignments requiring a high degree of technical and scientific capabilities, as well as provide leadership by directing the technical efforts of other team members. Your designs will use the latest technological advances in susbstrate technologies, MMIC device technologies, packaging technologies, and advanced simulator technologies. Experience Requirements: MS in engineering or BS in Engineering with specific applicable experience to be equivalent to the MS degree. Minimum of 10 to 12 years RF and Microwave Design Experience, strong usage and advanced applications of RF simulation tools (ADS, Sonnet, HFSS, etc) for use in highly detailed circuit design and analysis, Micro-electronic background (chip and wire level) along with complex Multichip Module design and layout, MMIC design and test experience. RF Multilayer CCA design and layout. Advanced scientific and technical concepts, advanced mathematics and the application of these concepts to electronics design and development. Proficient in Microsoft Office. Ability to obtain a Security Clearance. (US Citizenship required) ITT is an Equal Opportunity Employer.

Job Title: Supplier Integration Engineer Company: BAE Location: Wayne, NJ Description: Perform onsite assessments of supplier capabilities looking into their process controls and lean maturity Develop and propose new tools and procedures to support the development of preferred supply partners Recommend supplier-specific improvement opportunities and lean techniques that can be implemented to improve supplier performance in cost, quality, and lead time Provide applicable lean training to suppliers and facilitate Kaizen events if and when necessary Support the development of supplier improvement plans; provide guidance, expertise, and the necessary tools to support the execution of the plan Support the Commodity Team Lead in driving, tracking, and communicating supplier improvement progress against established goals Assess the effectiveness of the implemented lean improvements; follow up with the supplier to identify new areas for continuous improvement Identify areas for Cost Take Out (CTO) at the supplier site and work with the supplier to achieve; support the Commodity Team Lead to develop a means for tracking and measuring the cost savings Serve as the supply chain liaison to the supplier; link the required TAKT and material requirements needs back to the supplier (problem information, TAKT rate, other needs, etc) and help the supplier achieve the requirements Support the Commodity Team Lead(s) as required Support the Supplier Engineering & Supply Chain Organization as required; facilitate internal Kaizen events as requiredBS in technical field or equivalent experience as it relates to commodity expertise and minimum of eight (8) years work experience or Masters degree and six (6) years experience Black Belt or Green Belt certification is a plus Ability to plan and manage multiple initiatives simultaneously, formulate action plans for and execute those plans to drive initiatives through to completion. Creativity and ability to think outside of the box Possess a strong analytical and problem-solving skills Proficiency with continuous process improvement methodologies and tools; strong group facilitation Knowledge or experience in a role that required expertise in change management, process re-designs or re-engineering projects and methodologies Knowledge with lean manufacturing techniques such as; value stream mapping, kaizen, kanban, supplier managed inventories, point of use, milk runs, 5S, TPS, DFT, takt and cycle times, single piece manufacturing flow and six sigma Proven teamwork and leadership skills; able to work across boundaries including across multiple functions, program teams, suppliers Strong process knowledge with hands-on experience implementing lean principles Materials & scheduling knowledge a plus Strong written/verbal communication skills Computer proficiency, strong analytical thinking Must be willing to travel (greater than 5 %)BAE Systems is the premier global defense and aerospace company, delivering a full range of products and services for air, land, and naval forces, as well as advanced electronics, information technology solutions, and customer support services. With 1 5, employees worldwide, BAE Systems had 2 8 sales of $34.4 billion.Electronic Solutions, based in Nashua, New Hampshire, provides systems and products that maximize the effectiveness and safety of fighting forces and first responders. Its offerings include infrared countermeasures and electronic protection systems for military and civilian aircraft; information management systems; signal acquisition, analysis, and exploitation systems that optimize use of the electromagnetic spectrum by friendly forces while denying its use by adversaries; interoperable communications systems for firefighters and other first responders; thermal weapon sights; precision targeting systems; situational awareness systems for ground vehicles; night-vision systems; identification friend or foe systems; and radiation-hardened electronics. Electronic Solutions also includes the group?s Advanced Systems & Technology unit, which joins EI&S with government research organizations and industry to develop and demonstrate innovative system concepts in such areas as situational awareness, communications and networking, and precision targeting.People are the greatest asset in any Company ... BAE Systems is committed to a high performance culture and provides an environment that challenges our employees to be remarkable and obtain their full potential. We are an EEO/Affirmative Action Employer that understands the value of diversity and its impact on a high performance culture.

Job Title: Biologics Manufacturing Design and Validation Principle Engineer (Purification) Company: Discovery Solutions Location: Branchburg, NJ Description: Implementing the process validation program for the manufacture of biologicalsGENERAL SUMMARYThis position is responsible for implementing the process validation program for the manufacture of both new and existing biologicals. Responsibilities include planning, writing and managing the execution of process validation protocols, such as consistency and product comparability protocols. The authoring of manufacturing and validation sections of regulatory filings will be required. This position will report to a Sr. Director or Director in Manufacturing Technology and will interact with Engineering, Manufacturing, Validation, Quality Assurance, Quality Control and Regulatory Departments. Interaction may be required with contract producers of the company's products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is essential.ESSENTIAL DUTIES AND RESPONSIBILITIESResponsible for supporting manufacturing operations through the performance of the following duties:1. Plan and manage the execution of process validation studies, such as process consistency studies, performed for the company's products. The main areas of focus are purification and downstream processing activities. Author the required protocols, reports and regulatory documentation associated with the executed studies.2. Review and approve protocols and reports authored by other groups.3. Author relevant portions of drug substance manufacturing and process validation sections of regulatory filings.4. Author technical reports supporting technology transfers, deviation/adverse event reporting and process analyses/trending. This responsibility is shared with the Process Sciences Group.5. Support the Manufacturing Process Sciences Group, the Statistics and Quantitative Sciences Group and the Clinical Manufacturing Group as required.6. Consult with other groups to troubleshoot manufacturing process problems.7. Ensures cGMP compliance.EDUCATION AND EXPERIENCE:1. BS degree in Chemical Engineering (equivalent non-engineering title for Biochemistry, Chemistry, Microbiology degrees). 2. Minimum of 12 years experience in a GMP production/development environment.3. Has previously started-up and/or had a management role in a biotechnology facility.4. Has detailed process and equipment knowledge of protein purification processes and functions. Similar knowledge of cell culture processes a plus.5. Process validation experience required.6. Has a thorough understanding of cGMP requirements for a large scale manufacturing facility.7. Experience in successful facility licensure a plus.8. Excellent communication skills, both oral and written.9. Demonstrated supervisory skills.

Job Title: Master Black Belt/Process Re-engineer Company: Horizon-Blue Cross Blue Shield Location: Newark, NJ Description:  We are currently seeking a Master Black Belt and strategic-thinking leader to execute and manage enterprise-wide core process re-engineering initiatives. In this evolving role, you will lead cross-functional project teams and utilizing Six Sigma and Lean methodologies to evaluate business processes and determine initiatives that will provide greater productivity, efficiency and enable increased growth, as well as facilitate follow-up activities targeted toward increasing revenue, optimizing cycle time, reducing defect rates, and/or improving provider satisfaction.  The successful candidate must be able to quickly understand the business in order to recommend improved, strategic, measurable and sustainable solutions as well as identify further opportunities for improvement.  Responsibilities: Evaluating existing Provider Network Management processes and recommends improved, strategic, measurable and sustainable solutions, as well as identifies further opportunities for improvement. Leading strategic, cross functional, complex process improvements projects targeted toward increasing revenue, optimizing cycle time, reducing defect rates, and/or improving provider satisfaction. Providing continuous coaching, direction and follow up to project teams to ensure on-time, high-quality deliverables and goal achievement. Developing monitoring systems for the collection, documentation and reporting of quality assessment and improvement data. Extracts pertinent information from quality assessment and improvement studies, initiates corrective action plans, and re-monitors results.Partnering with the senior management team to identify, quantify, prioritize, and implement performance improvement initiatives for the organization.Maintaining effective communication with managers and senior leadership regarding the status of quality and performance improvement projects. Acting as a resource and mentor to Black Belts, Green Belts, Champions, and business units in identifying, planning and implementing Six Sigma projects.  To qualify for this opportunity, you must possess the following: Minimum 5 - 7 years in a leadership role in Process Improvement and Productivity and Quality Improvement. Demonstrated experience in leading strategic change initiatives across large corporate organizations, process re-engineering and improvement methodologies, development of metrics programs, benchmarking, management training and internal/external client satisfaction programs.Proven ability to deploy LEAN, Six Sigma and/or Total Quality Management process improvement methodologies, and ability to tailor programs to meet the needs of the organization.Superior critical-thinking ability and problem-solving skills to deal with highly complex, cross functional processes and strategic projects.Exceptional communication and team-building skills. Ability to influence, negotiate and accelerate change across all levels of the organization. Black Belt certification required; Master Black Belt certification strongly preferred. Bachelor’s degree required; Master’s degree preferred. Horizon Blue Cross Blue Shield offers competitive salaries, a dynamic work environment and tremendous opportunity for career growth and development. Our comprehensive benefits package includes health, dental, vision and life insurance; tuition reimbursement; 401K savings plan; retirement savings plan; work-life balance programs; onsite amenities including a fitness center, cafeteria, health center, pharmacy and day care; and much more. Please submit an online application, with a resume attached, to www.horizonblue.com/careers. EOE/AA M/F/D/V

Job Title: Electrical Quality Engineer - Me Company: Biomet, Inc. Location: New Brunswick, NJ Description: Electrical Quality Engineer - Medical DeviceDate Posted:Monday, February 15, 2010Department:EngineeringLocation:Parsippany, NJRequirements:Biomet, a leading manufacturer of orthopedic devices, is seeking an Electrical Quality Engineer - Medical Device, for its Parsippany, NJ office. This position provides quality engineering support for product realization and manufacturing of Class III Bone Stimulation Systems.Essential Duties and Responsibilities include the following.Other duties may be assigned.* Represent Quality Engineering and Regulatory Compliance on project teams to ensure compliance with Biomet, FDA, ISO Quality System Requirements.* Assists in the development of inspection plans which define appropriate quality inspection techniques and methodologies.* Assist product development and manufacturing engineering with appropriate disposition of rejected product (DMRRs).* Design review of electrical product drawings for potential quality issues, GD&T, manufacturability and conformance to applicable standards.* Provide technical support on product requirements and specifications for new products in the preliminary design phase. Coordinate and assist in the design, research & development of new product introductions.* Conduct failure analysis investigations, and risk analysis of reported events. Supervise and provide guidance to electronic technicians in failure analysis of Bone Stimulation products.* Provide assistance for external supplier auditing and supplier control, and provide assistance during internal audits of electrical development activities.* Collaborate with engineering, manufacturing, and marketing to identify and coordinate efforts toward corrective action where quality problems have been identified. Implement quality cost reductions through corrective and preventative actions.* Assist in the development, execution, and maintenance of software, process and manufacturing equipment validation protocols (IQ, OQ, PQ).This position is for a Mid to Senior level Electrical Engineer with the safety, regulatory, and electrical component design and troubleshooting experience to maintain compliance with FDA Quality System Requirements (QSR) and ISO 13485:2003 requirements for Class 3 Medical Devices.The ideal candidate must possess the following:* BS in Electrical Engineering and 4-5 years in medical device quality assurance.* Must have prior experience with Class II and Class III medical devices (and/or active implantable).* Must have experience leading the development of product Risk Management per ISO 14971, including development of Hazard Analysis and DFMECA.* Applied working knowledge of QSR, ISO 13485:2003, JGMP, MDD, and AIMD. Quality engineering statistical analysis including DOE, MSA, reliability engineering, sampling plans, t-test, f-test, ANOVA, and SPC.* A working understanding of FDA Quality System regulations, EU Active Implantable and Medical Device Directives, and ISO 13485:2003 principles.* Knowledge of IEC 60601 medical device safety standards and IEEE software quality standards is preferred.* Must have good verbal and communication skills, and the ability to multi-task.* Must have good PC skills, and be proficient with the following: Microsoft Office (Excel, PowerPoint, and Word) Agile, and Mapics.* Familiarity with common support IC's and battery cell technologies. Knowledge of popular schematic capture applications is a plus.* Experience and ability to analyze chip use, analog and digital, as needed to check operating margins (if necessary).* PCB layout, especially those for surface mount devices, is desirable.Strong Qualifications in:* IEC/IN 60601-1-1 (5 years medical - general requirements for electrical equipment/systems safety and /electromagnetic compatibility - requirements and tests)* FDA Quality Systems Requirements and ISO 13845:2003 (5 years -with ISO 9001 substitutable)* 21 CFR 820.30 (5 years QSR design controls for medical devices)* Risk Management per ISO 14971 (5 years hazard analysis, failure mode effects criticality analysis, hazard mitigation, etc.)* Software & Hardware Troubleshooting and Resolution Recommendation (5 years component level troubleshooting and providing Supplier corrective/preventive actions)Biomet offers an attractive compensation package including dental, 401(k), and tuition reimbursement. Only those candidates who meet these qualifications will be evaluated. For confidential consideration, submit resume with salary history to: Register to View Biomet is an Equal Opportunity Employer.

Job Title: Principal Engineer (IRC1165) Company: Integra LifeSciences Corp Location: Plainsboro, NJ Description: Integra LifeSciences Corporation is a world leader in developing and marketing high quality surgical instruments, as well as innovative devices and products for use in neurosurgery, reconstructive surgery, general surgery and soft tissue repair.  Integra has increased revenues over 40% annually over the last 10 years.  We anticipate our significant growth to continue as we celebrate 20 years of clinically relevant, innovative and cost-effective products.  In 2005, 2006, and 2008 Integra LifeSciences was named to the Forbes 200 Best Small Companies list.  In 2007 Integra was named Medical Device Manufacturer of the Year by Medical Device & Diagnostic Industry Magazine, and was selected as the New Jersey Technology Council's Master Technology Company of the Year. Reporting to the Engineering Manager, this position is responsible to execute & manage project assignments in the evaluation, selection, and application of various engineering techniques, procedures, and criteria with minimal supervision. Independently plans, schedules, and leads detailed phases of the engineering work in a part of a major project or in a total project of moderate scope. Solves basic and complex problems identified through process characterization, monitoring & trending. Apply innovative approaches in the development of new processes, equipment, & systems. The incumbent should be able to complete complex design and engineering tasks and manage projects with little assistance. This includes constructing detailed, accurate project schedules, interfacing with internal and external engineering & technical resources in solving project problems, and having the ability to prioritize multiple projects and tasks.   To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. ?         Responsible for process engineering and project management to support improvement of existing processes, and introduction of new product & processes. These projects are typically higher level capital projects with increased complexity, and can pose significant risk to product and processes if not designed and implemented correctly.?         Responsible for liaising with Product development group to  provide plant input in the product development process, to include but not limited to, design requirements, risk analysis, traceability matrix, design history file, etc.?         Responsible for total Project management, process development, process improvement, IQ/OQ/PQ validations, and Manufacturing process troubleshooting. Must be able to manage the project in its entirety, and be able to perform / deliver specific project tasks as necessary.?         Responsible for analysis and upgrade of utility systems when needed (WFI, DIUF, Lyophilizers, HVAC, CCA, & steam generation)?         Perform timely technical investigations and provide practical manufacturing solutions, under appropriate regulatory guidelines for Medical Device Manufacture.?         Provide daily analytical and technical support to meet manufacturing objectives.   ?         Assemble and lead technical teams for identified projects and products, which may include personnel from Engineering, Manufacturing, Product Development, Marketing, QA, and Clinical & Regulatory Affairs. ?         Work closely with Development Engineers, Marketing, Sales, and Clinical colleagues to ensure smooth transfer of product and process scale-up.?         Apply experience with manufacturing process equipment to lead the selection and/or design of equipment for prototype and full scale manufacturing?         Lead teams in performing and updating Process FMECA risk management?         Effectively implement problem solving skills and techniques to identify potential issues, assess their impact and develop and implement mitigation and resolution plans and activities?         Coordinate specific efforts of the project team, including the core team members (Manufacturing, Plant QA/QC/RA, Facilities, Materials Management, and Engineering) and supporting members (Corporate Regulatory, Finance, etc.). Includes such tasks as development of Manufacturing requirements, accounting documentation, specifications, validations, and Engineering drawings and ECN paperwork.?         Ensure that all appropriate documentation, drawings specifications are generated in compliance with Integra?s procedures and statutory requirements ( US FDA and ISO)?         Responsible for process scale up to plant standards and manufacturing volumes.?         Provide technical input for analysis of process changes?         Develop P&ID and PFD as required?         Working knowledge of Automation & PLC required?         AutoCAD experience required   DESIRED MINIMUM QUALIFICATIONSThe requirements listed below are representative of the knowledge, skill, and/or ability required. ?         MS in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or equivalent.  ?         Minimum of 15 years experience in the medical device, pharmaceutical industry, or chemical industry with experience in process development. ?         Experience with Quality System Regulation (QSR), Design Control and Process Validation guidelines, Engineering Change Controls, QSR, ISO, and Design Control and Regulatory procedures is required. Experience in clean rooms, Lyophilization a plus.?         Experience in biomaterials desirable. ?         General chemistry, processing and materials expertise ?         Exceptional practical problem solving skills, excellent organizational and communication skills ?         Practical product fabrication a plus. ?         Use of statistical process tools highly desirable. Minitab a plus. ?         Six Sigma  training highly desirable?         PE certifivcation a definite plus. We are committed to creating an environment where all employees are valued and respected.  We offer a competitive benefits package including 401(K) savings plan with match, medical, vision, dental, life insurance, tuition reimbursement, and employee stock purchase plan.To find out more about our company, visit our website at: http://www.integra-ls.com No Agencies.  LOCAL CANDIDATES ONLY PLEASE.  EOE, M/F, D/VIntegra is not currently accepting unsolicited assistance or resumes from search firms for this employment opportunity.  All resumes submitted by search firms or agencies to  Integra or its employees, agents, directors or representatives in any form or method without a valid written agreement covering this  position will be deemed the sole property of Integra.  No fee shall be paid in the event the candidate is hired by Integra as a result of the referral or through other means. Search firms are essential to the recruitment and staffing efforts at Integra and we value the partnerships we have built with our preferred vendors. For this reason, Integra has established and regularly maintains a vendor list. Please note that even preferred vendors are required to have a written search agreement signed by an authorized signatory of Integra in order for a fee to be paid for any candidate referrals. Please click the following URL to apply for this job https://erpiapps.integra-ls.com/OA_HTML/OA.jsp?OAFunc=IRC_VIS_VAC_DISPLAY&p_svid=1165&p_spid=33285&p_site_id=21

Job Title: Sr. Power Electronics Engineer (Sustaining Engineering) Company: Company Confidential Location: Piscataway, NJ Description: This is one exciting and growing company that will define a new era for it's respective employee as the company is positioned for 200% growth in the next 2 years and has quickly become the leader in it's respective renewable energy sector. Summary: Responsible for the technical design aspects of all products that have been released to production. Will be required to identify and implement continuous improvements to these products in order to increase production yield and improve reliability. Will work within the Engineering Department to ensure the smooth transition of new products into production.  Will interact with people in various other departments throughout the organization to resolve issues, answer questions, and provide product training.  Interaction with vendors and contract manufacturers will also be required.  Will analyze high reliability, small/micro-electronics circuitry for DC-DC power converters and related devices.  Improve products by suggesting innovative circuit designs, updating documentation, conducting analysis, and characterization.  Manage multiple projects including scheduling preparation and reporting.  Provide mentoring and training to other engineers. Essential Functions:Knowledge of design elements including, inverter design, u-Controller algorithm development, wireless RF design, EMI filtering, transient protection, analog design, component selection, simulation/test, PCB layout, and product functional specification. Will participate in, circuit analysis, bread boarding, hardware requirements analysis and derivation, reliability studies, and design verification testing. Be involved in continuing engineering maintenance and manufacturing floor support of existing products. Recommend changes in circuitry or installation documents to improve assembly, maintenance, testing methods or product performance. Analyze and interpret test data. Adjust, calibrate, align and modify circuitry and components and record effects on unit performance. Participate in the test, troubleshooting, diagnosis, and root cause analysis of sub-assembly and system-level problems down to the component level.  Generate recovery plans and corrective action.   Proactively define and suggest improvements to the design engineering environment as well as areas unrelated to engineering. Provides overall project planning for activities surrounding released products including schedules, generating test and qualification plans, and updating specifications. Oversees the accuracy and maintenance of the full documentation package for all released products including but not limited to: BOMs, operator manuals, test procedures, process sheets, work instructions, etc. Work with and provide detailed defect data to Manufacturing, Engineering, and Quality organizations. Interfacing with cross-functional departments: marketing, manufacturing, quality and senior management, and external customers. Implement engineering change instructions. Working with Engineering Technicians. Perform other job-related duties as assigned.  To apply for this position, please Email your resume to Lou Petto:  Register to View

Job Title: Electrical Quality Engineer Medical Device Company: Biomet Location: Parsippany, NJ Description: Biomet, a leading manufacturer of orthopedic devices, is seeking an Electrical Quality Engineer – Medical Device, for its Parsippany, NJ office. This position provides quality engineering support for product realization and manufacturing of Class III Bone Stimulation Systems. Essential Duties and Responsibilities include the following. Other duties may be assigned. · Represent Quality Engineering and Regulatory Compliance on project teams to ensure compliance with Biomet, FDA, ISO Quality System Requirements. · Assists in the development of inspection plans which define appropriate quality inspection techniques and methodologies. · Assist product development and manufacturing engineering with appropriate disposition of rejected product (DMRRs). · Design review of electrical product drawings for potential quality issues, GD&T, manufacturability and conformance to applicable standards. · Provide technical support on product requirements and specifications for new products in the preliminary design phase. Coordinate and assist in the design, research & development of new product introductions. · Conduct failure analysis investigations, and risk analysis of reported events. Supervise and provide guidance to electronic technicians in failure analysis of Bone Stimulation products. · Provide assistance for external supplier auditing and supplier control, and provide assistance during internal audits of electrical development activities. · Collaborate with engineering, manufacturing, and marketing to identify and coordinate efforts toward corrective action where quality problems have been identified. Implement quality cost reductions through corrective and preventative actions. · Assist in the development, execution, and maintenance of software, process and manufacturing equipment validation protocols (IQ, OQ, PQ). This position is for a Mid to Senior level Electrical Engineer with the safety, regulatory, and electrical component design and troubleshooting experience to maintain compliance with FDA Quality System Requirements (QSR) and ISO 13485:2003 requirements for Class 3 Medical Devices. The ideal candidate must possess the following: BS in Electrical Engineering and 4-5 years in medical device quality assurance. Must have prior experience with Class II and Class III medical devices (and/or active implantable). Must have experience leading the development of product Risk Management per ISO 14971, including development of Hazard Analysis and DFMECA. Applied working knowledge of QSR, ISO 13485:2003, JGMP, MDD, and AIMD. Quality engineering statistical analysis including DOE, MSA, reliability engineering, sampling plans, t-test, f-test, ANOVA, and SPC. A working understanding of FDA Quality System regulations, EU Active Implantable and Medical Device Directives, and ISO 13485:2003 principles. Knowledge of IEC 60601 medical device safety standards and IEEE software quality standards is preferred. Must have good verbal and communication skills, and the ability to multi-task. Must have good PC skills, and be proficient with the following: Microsoft Office (Excel, PowerPoint, and Word) Agile, and Mapics. Familiarity with common support IC’s and battery cell technologies. Knowledge of popular schematic capture applications is a plus. Experience and ability to analyze chip use, analog and digital, as needed to check operating margins (if necessary). PCB layout, especially those for surface mount devices, is desirable. Strong Qualifications in: · IEC/IN 60601-1-1 (5+ years medical - general requirements for electrical equipment/systems safety and /electromagnetic compatibility – requirements and tests) · FDA Quality Systems Requirements and ISO 13845:2003 (5+ years -with ISO 9001 substitutable) · 21 CFR § 820.30 (5+ years QSR design controls for medical devices) · Risk Management per ISO 14971 (5+ years hazard analysis, failure mode effects criticality analysis, hazard mitigation, etc.) · Software & Hardware Troubleshooting and Resolution Recommendation (5+ years component level troubleshooting and providing Supplier corrective/preventive actions) Biomet offers an attractive compensation package including dental, 401(k), and tuition reimbursement. Interested applicants must submit their resumes, which must include salary requirements, to Register to View , Attn.: QE EEO/AAP

Job Title: Principal Engineer - Packaging Company: BD (Becton, Dickinson and Company) Location: New Brunswick, NJ Description: Title: Principal Engineer - PackagingLocation: New Jersey-Franklin LakesHigh Impact position responsible for developing & executing strategies for sustainable medical device packaging, supporting BD's environmental sustainability initiative.The candidate will be a dedicated Technical Lead for identifying, managing & delivering green packaging for new and existing medical devices across multiple product platforms. Specific responsibilities include,* Bring expertise in designing for green and life cycle analysis in identifying & evaluating materials, designs, and configuration of primary, secondary, and other packaging levels, as applicable, optimizing carbon footprint, customer benefit and the supply chain requirements* Identify, evaluate & recommend new packaging materials for cost effectiveness, recyclability & re-usability* Development and Validation (per design control requirements) of packaging components, designs and processes/technologies for various sterilization modes preserving the safety and efficacy over the shelf life* Evaluates new packaging concepts and technologies using engineering first principles* Create prototypes, drawings, specifications, test instructions for customer approval, external testing and tooling requirements.* Work directly with suppliers to qualify new materials / designs* Visit / interview external customers to gather Voice of customer related to packaging* Proactively develops and maintains technical knowledge in specialized area(s), remaining up-to-date on current trends and best practices. Actively teach and promote learning.* Provide Project Leadership to cross-functional teams comprising QA, purchasing, product R&D, MA, RA, marketing, manufacturing engineering, sterilization sites.* Independently plan, implement, delegate, monitor and deliver designated tasks and deliverables.* Effectively lead and direct the work of other engineers and laboratory technicians to achieve objectives.* Ensure compliance with BD quality policies, procedures and practices as well as with all local, state, federal and BD safety regulations, policies and procedures.*Minimum: MS degree in Materials Science, Industrial Design or other technical discipline (Polymers, Design, Mechanical, Packaging) with at least 4 - 6 years direct, relevant experience.*Experience in the medical device or pharmaceutical industry is preferred.*Ph.D. in above disciplines with 2 years relevant experience is preferred*Lean / Six Sigma preferred*Design packages for green consideration*Experience developing packaging green strategy*Life cycle analysis and strategic tradeoff between materials/ design*Experience in at least one environmental sub-field, such as carbon accounting, life cycle assessment, sustainable materials, or waste management*Experience with rigid and flexible forming materials and technologies (corrugate, paper board materials, F/F/S, Flow wrap)*VOC analysis*Experience with Package processing equipment & process development package loading*On line labeling & printing experience*Familiarity with blow molding, injection molding, and film extrusion*Leading Lean/Six Sigma projects preferred* Fundamental package design principles & techniques*Packaging design software (e.g. TOPS, CAPE, ArtiosCAD)*Excellent cross-functional influencing skills*Understanding of disciplined product development processes*Strong Organization skills*Sound technical judgment*Working knowledge of ISO, FDA and international regulatory and quality requirements applicable to Medical Device Packaging*Knowledge of environmental science principles and ecological impacts*Design and statistical analysis of experiments*Project planning*Value stream analysis, preferred

Job Title: Sr. Reliability Engineer Company: Merck Location: Whitehouse Station, NJ Description: Description Job Description Job Title: Sr. Reliability Engineer Job ID: 33051 Location: GA, Atlanta Full/Part Time: Full-Time Regular/Temporary: Regular Position Details Leadership position within Cox Corporate Engineering to help develop and implement the overall program relative to reliability in areas of network design, maintainability, life cycle costs and field performance. Key Responsibilities 1.Develop tools, techniques, measures and program that can be used to model/simulate reliability of designs prior to network deployment. 2.Analyze the results to highlight advantages/concerns with hardware, software and life cycle costs (including maintainability). 3.Incorporate recommendations of designs as part of the planning process to ensure the best overall solution is selected.  4.Follow-up on analysis to ensure trending is tracking to prediction. 5.Develop tools, methods, measures and program of tracking/improving field reliability and performance of network components.  6.Analyze information, providing opportunities for improvement.  7.Develop plans and implement improvement initiatives with internal partners and product suppliers that reduce overall outages and failures in the network (e.g. vendor/supplier quality programs). 8.Develop and implement programs centered on reducing overall life cycle cost (including optimized maintenance strategies and reduction of repair intervals). 9.Provide guidance and direction on service level agreements and ensure methods exist to measure compliance. 10.Participate in government sponsored reliability forums as necessary (e.g. NRIC). Qualifications 1.Typically requires BS/BA in EE, MIS, CIS or related discipline. Generally 5-8 years of experience in related field. MS/MA and generally 3-5 years of experience in related field. Certification required in some areas or specialized training in reliability engineering 2.Minimum of 5 years experience in an applicable technology discipline performing a reliability engineering role. 3.Demonstrated knowledge and experience in reliability engineering tools and methods including: 4.Basic/advanced statistics (e.g. SPC, confidence intervals, hypothesis testing, probability/PDF, MLE, discrete/continuous distributions such as Weibull/Poisson and DOE). 5.Reliability block diagrams (RBD) and reliability modeling techniques. 6.Reliability simulation techniques (e.g. Monte Carlo, Markov, etc.). 7.H/W and software reliability predictions (e.g. MTBF, FITS, failure rate, availability, software reliability engineering, etc.) 8.Warranty or spares analysis 9.Failure mode and effects analysis (FMEA and also FMECA). 10.Corrective and prevent action programs. 11.Six Sigma green belt / black belt a plus. 12.Demonstrated project management skills. 13.Telecommunications, data or network engineering experience in an engineering role is highly desired Dept/Org Scope & Impact - Seasoned professional contributor with responsibility for an advanced area of work in the professional field; May be responsible for entire projects or functions having modest scope/impact or portions of projects having considerable scope/impact to department, area, and, at times, business unit results Problem Complexity - Performs advanced areas of work for the professional field; Identifies key barriers/core problems and applies problem-solving skills in order to deal creatively with complex situations. Troubleshoots and resolves complex problems Autonomy - Independently performs assignments with instruction limited to results expected. Determines and develops approach to solutions; Receives technical guidance only on unusual or complex problems or issues Knowledge - Possesses and applies comprehensive knowledge of particular field of specialization to the completion of complex assignments. Advanced knowledge of organization's technologies and practices Primary contribution is in applying knowledge (product, industry, professional, technical) rather than managing people.  Greater than 50% of time is doing individual contributor work No responsibility for developing and managing operating plans/budgets Influence/People Leadership - May oversee the completion of projects or assignments, including planning, assigning, monitoring, and reviewing progress and accuracy of work, evaluating results, etc.; Contributes to employees' professional development, but does not have hiring or firing authority Cox Communications, Inc. and its subsidiaries are Equal Opportunity Employers. We have a tradition of encouraging a wide diversity of talents through a broad range of hiring practices. Please note those individuals submitting resumes online or by mailing a resume are not considered an applicant for employment until a signed employment application form is completed, usually at the time of interview. For more information about Cox Communications and its subsidiaries, please click here www.cox.com, www.coxmedia.com, www.coxbusiness.com. Statement to ALL Third Party Agencies and Similar Organizations: Cox Communications accepts resumes only from agencies with which we formally engage their services.   Please do not forward resumes to our applicant tracking system, Cox Communications employees, or send to any Cox Communications facility. Cox Communications is not responsible for any fees or charges associated with unsolicited resumes.