C.R. Bard Jobshttp://crbard.jobs2012-05-23 10:36:26.613562USAMurray HillQA RA Associate Industry Title /Category: Quality Assurance / Regulatory Affairs Job ID: 2012-5662 Career Level: experienced Location/Division: International Relocation: No Posted Date: 5/21/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: This position is responsible for managing key administrative projects for the Asia Regulatory Affairs and Quality Assurance Department with primary focus on customer complaint handling, coordinating regulatory tasks, as well as providing department administrative support where needed. In addition, this position will provide backup support and work closely with the Latin America Regulatory Affairs and Quality Assurance department (i.e. vacations, time out of office etc.) for complaint management. Summary of Position with General Responsibilities: • Coordinates full spectrum of complaint handling on behalf of Asia geographies. • This includes entering complaint data into the database, coordination of sample returns; gather any additional information requested by the manufacturer for the complaint investigation and the drafting of customer letters. • Wide interaction and communication with all Asia IBC’s and Divisions to assist with entry and closure of complaints. • Prepare and maintain various complaint and MDR reports and metrics, and provide monthly summary on complaints by countries. • Provide supports to miscellaneous regulatory tasks (i.e. update the monthly report on Asia registration status, maintain the tracking log of IBC requests, legalization of regulatory documentation, etc.) • Assists the department head in other administrative duties (i.e. schedule meetings/travel supplies, etc.). Essential Job Functions: Basic Qualifications: * High level of proficiency in the use of a computer with intermediate level of keyboarding skills and proficiency in the use of Outlook, Word, Excel, and PowerPoint. * Strong interpersonal skills in the areas of verbal and written communication, telephone courtesy and professionalism. * Strong organizational skills and the ability to take initiative for assigned projects. * Attention to detail and the ability to maintain confidentiality of product registration documents. * Ability to prioritize and handle several projects concurrently. * Must be self-motivated and have ability to take ownership of her/his responsibilities. * Must be a team player and capable of working with minimal supervision. * Must be able to set goals and accomplish them within a set time schedule and budget. Basic Qualifications: Education and/or Experience: • Two-year associate degree or equivalent. • Science major preferred. • Eight+ years minimum office administration/coordination experience in a fast paced environment. • Minimum three years experience working in a medical device-related environment required.2012-05-21 19:29:35United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ28835512http://crbard.jobs/xml/28835512/jobUSAMurray HillERP Programmer / Analyst Industry Title /Category: ERP Programmer Job ID: 2012-5489 Career Level: experienced Location/Division: Murray Hill Relocation: No Posted Date: 2/23/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: Applies system solutions to business problems though the design and programming of automated systems. Works on multiple projects as a project team member, occasionally as a technical leader. Works on small to large, complex projects that require skill in multiple technical environments and knowledge of a specific business area. Applies knowledge and experience with technology and application development methodologies to perform basic systems analysis techniques, testing, debugging, file design and storage. Summary of Position with General Responsibilities: Essential Job Functions: • Focused on ERP applications • Configures, analyzes, designs, develops, and maintains ERP program codes and applications to support business processes and functions • Performs all aspects of programming assignments and assists with system design • Develops project functional requirements • Finalizes project and system documentation • Monitors assigned projects to insure that predetermined deadlines are met • Tests all modules to ensure quality • Provides problem resolution for assigned software • Provides user assistance with assigned applications • Analyzes specifications for completeness and accuracy • Leads maintenance to existing applications • Adheres to ITS standards, policies and procedures • Provides technical support to teams Essential Job Functions: Basic Qualifications: * Strong JDEdwards E1development skills * Must have work experience with all facets of the JDE E1 Software Development toolset (OMW, ER, RDA, FDA, JDE C Business function, etc.). * Must be able to troubleshoot issues using various debug methods including debugging JDE C business functions. * Working knowledge of Order to Cash processes * Working knowledge of Oracle Database applications Additional Desirable Qualifications Skills and Knowledge: * Ability to develop information solutions based on business requirements * Understand process and deliverables associated with each systems life cycle phases * Ability to determine balance between systems development and maintenance efforts * Knowledge of appropriate hardware and software required for application development * Knowledge of office productivity tools Education and/or Experience: * Bachelor’s Degree in Computer Science, Information Systems, or other related field. Or equivalent work experience * 3 to 5 years of IT work experience in programming and/or ERP systems analysis * Advanced programming techniques and software design * Knowledge of ERP applications or object oriented analysis and design2012-04-11 12:36:37United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ27814946http://crbard.jobs/xml/27814946/jobUSAMurray HillClinical Research Associate II (CRA II) Industry Title /Category: CRA Job ID: 2012-5516 Career Level: experienced Location/Division: Murray Hill Relocation: No Posted Date: 3/7/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: Mid-level clinical trial monitoring position within Corporate Clinical Affairs Operations Group. The CRA supports the day to day operations associated with the execution of clinical trials. The primary objective and purpose of this position is to ensure the overall quality of clinical trials by monitoring study data and managing site adherence to the protocol, GCP, all applicable regulations and related study documents. The CRA is the primary contact with the study site and serves as the liaison between clinical investigators and Bard. The CRA is responsible for site training, regulatory document collection, tracking enrollment, and ensuring case report forms are accurate, complete and verifiable against source documents. The CRA will monitor multiple clinical trial sites and studies. The CRA is expected to contribute to the development and improvement of company procedures, processes, and templates in support of Bard’s efforts towards continuous quality improvement. Ability to prioritze workload to meet study timelines while monitoring multiple protocols • Perform monitoring visits: o Qualify potential investigative sites; o Train and initiate investigative sites; o Conduct routine monitoring visits and close out visits; o Complete monitoring trip reports accurately inventoried and documented; o Review case report forms to ensure data compliance; o Account for investigational devices ensuring the devices are available, stored appropriately, and accurately inventoried and documented; o Verify appropriate reporting and documentation of adverse events and protocol deviations per protocol requirements; o Ensure site regulatory binder is current. • Manage investigative sites from study start up through close out: o Provide support to the investigator evaluation and recruitment process; o Assist in the collection of initial regulatory documentation; o Assist in the preparation of study binders, manuals, or other site specific tools. • Assist in the developmentof study specific monitoring tools. • Perform study tracking activities as requested. • Assists CRA Manager in development of Clinical Monitoring Plan. • Ability to work with little supervision Summary of Position with General Responsibilities: Ability to travel up to 50%. Certification (CCRA) through ACRP preferred, but not required BS / BA in a related scientific area; • Knowledge of clinical trial methodology relating to the monitoring of clinical trials, GCP, FDA, and / or country specific regulatory environment; • Minimum of 3 - 6 years of field monitoring experience; • Medical device experience preferred, but not required; • Proficient in MS Office Suite of products; • Experience with Clinical Trial Management System preferred; • Experience with EDC system preferred; • Excellent interpersonal and communication skills; • Proven ability to demonstrate strong decision making and problem solving skills.2012-04-11 12:36:21United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ27814933http://crbard.jobs/xml/27814933/jobUSAMurray HillExecutive Assistant Industry Title /Category: Executive Assistant Job ID: 2012-5553 Career Level: experienced Location/Division: Murray Hill, New Jersey Relocation: No Posted Date: 3/29/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: Summary of Position with General Responsibilities: This position is responsible for providing day-to-day administrative support to division Controller, Supply Chain Director and Customer Service Manager. Essential Job Functions: • General administrative duties such as typing, faxing, filing, Fedex/DHL mailings and mail distribution. • Heavy calendar management and international travel. • Coordinate complex, international travel arrangements and itineraries. • Organize meetings across multiple time zones. • Consolidate information for monthly reporting purposes. • Preparation and submission of expense reports and check requests. • Facilitate flow of documents that require signature. • Assist international staff with travel to Murray Hill office and other tasks as needed. • Assist in presentation preparations. • Flexible schedule required to meet demands of multiple international geographies. • Manage and maintain customer price files. • Maintain FCPA files and follow up to ensure records are complete and up-to-date. • Other duties as assigned. Summary of Position with General Responsibilities: Basic Qualifications: • Solid computer skills- Microsoft Word, Outlook, Excel and PowerPoint. • Minimum 5-7 years experience in an administrative role supporting multiple executives. • Prior experience supporting global executives. • Prior experience assisting a financial executive in a sales-based company. • Outstanding organizational skills. • Ability to manage confidential information. • Excellent oral and written communication skills. • Ability to manage and prioritize multiple tasks and deadlines. • Demonstrates initiative and is proactive.2012-04-11 12:35:51United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ27814890http://crbard.jobs/xml/27814890/jobUSAMurray HillQualitySystems Engineer/Sr. Engineer Industry Title /Category: Quality Systems Engineer Job ID: 2012-5475 Career Level: experienced Location/Division: Murray Hill Relocation: No Posted Date: 2/15/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: Summary of Position with General Responsibilities: The purpose of this position is to assist Quality Assurance Management with the compilation and analysis of operational metrics and preparing and presenting monthly and quarterly RGL/Management Reviews for Corporate Executive Management and recommending changes for Quality System improvements. The Quality Systems Engineers will lead/participate on company-wide Quality Improvement Projects. Additionally, the Senior Quality Engineer functions as a subject-matter resource for Engineering, Operations, and Quality Assurance. Essential Job Functions: *Collect and analyze monthly and quarterly quality performance metrics and other data using appropriate methodologies, statistics and tools that monitor and measure all aspects of the corporate quality system. *Prepare and assist in the reporting of the Management Review metrics to corporate executive management. *Provide strategies for corporate-wide Quality Systems improvements as well as strategies for improving the collecting and reporting process of the management review data and implement same. *Establish ownership of corporate quality information system(s) and provide guidance, assistance and training as a subject matter expert on same. *Compile, prepare and assist with the evaluation of Division recall plans when submitted for corporate review. *Write and approve validation protocols and reports including software validation. *Execute software/process validations. *Manage FDA inspection records. *Assists with Quality Systems or targeted Quality Audits. Basic Qualifications: Basic Qualifications: * Ability to understand and apply statistical and systems improvement tools to improve and sustain the corporate quality system. *Knowledge of medical device regulation, industry or international standard, including management responsibility. *Project Management skills, including basic team leadership skills, and good organization skills *Ability to understand Corporate, Division and Plant Quality Systems and be able to implement systemic changes to enhance product quality and improve business efficiency. • Strong organizational, practical mathematical (statistical) skills, analytical and problem solving skills. • Strong communication, presentation, interpersonal, and organizational skills. • Ability to apply quality control theories and principles to an operational environment. • Six Sigma or Lean skills and tools exposure advantageous. • Computer literate; able to utilize MS Office Suite, MS Project various database platforms and custom applications software. Additional Desirable Qualifications Skills and Knowledge: Additional Desirable Qualifications Skills and Knowledge: ASQ Certification (CQE, CRE, CQM etc.) a plus. Education and/or Experience: BS Degree in Science, Engineering or equivalent. Data management/analysis experience in the medical device or pharmaceutical industries is desired 3+ years experience with Quality Assurance programs in a corporate environment preferred2012-02-15 18:35:40United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ26538095http://crbard.jobs/xml/26538095/jobUSAMurray HillSenior Internal Auditor Industry Title /Category: Medical Device/ Audit Job ID: 2012-5432 Career Level: experienced Location/Division: Murray Hill, NJ/ Corporate Relocation: None Offered Posted Date: 2/28/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: The purpose of the Senior Internal Auditor position is to assist the Managers and Staff VP of Internal Audit in carrying out the duties assigned by Executive Management and the Audit Committee of the Board. Approximately 1/3rd of the candidates time will be dedicated to assisting our external auditors (KPMG) in performing certain Divisional audits and control reviews in conjunction with KPMG's annual audit (part of our internal/external audit reliance plan for 2012). The remaining 2/3rds of their time will contribute to various Balance Sheet, internal control, and SOX/FCPA/Advamed compliance reviews to be performed as part of our annual Internal Audit Plan. Candidate will also assist with review and coordination of Sarbanes-Oxley control documentation and testing. Role includes special projects, cost savings initiatives, etc. as the need arises. As part of each individual engagement, the candidate is expectd to contribute to the development of a work plan and audit objectives in each area being reviewed. This includes scoping, project flows, sharing project responsibilities between team members, execution of detailed testing, and documentation of work performed. They will be expected to draft written audit reports, and subsequently follow-up on progress made. Overnight travel (about 30-35%) is required to visit field locations. Approximately 75% of travel is domestic and 25% international is international, primarily in Europe. Long term mobility is a strong consideration. A two to three year in audit is expected. Goal is to develop a well-rounded individual to move on as a future accounting manager, seeking a Controller/Finance career path. Summary of Position with General Responsibilities: Excellent communication skills (both written and verbal) • Skilled at making presentations to Management and able to effectively sell ideas • Must be self motivated, have a passion for client service and strong desire to obtain new skills • BS/MS degree (must be eligible for CPA designation) - GPA of 3.0 or higher • MUST BE A Certified Public Accountant (CMA or MBA is a plus) • 3-5 years experience in public accounting, big 4 Firms preferred. • Must be familiar with and able to accurately interpret U.S. GAAP. • Experience with manufacturing entities is strongly desired. • SEC client experience a plus. • Strong analytical skills required to gather, interpret and present findings. • Experience with Multi-location and international locations preferred. • Working knowledge of Sarbanes -Oxley and COSO requirements required. Physical Demands: 25%-35% - Travel2012-02-06 20:20:15United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ26338753http://crbard.jobs/xml/26338753/jobUSAMurray HillAssistant General Counsel - Compliance Industry Title /Category: General Counsel Job ID: 2012-5399 Career Level: experienced Location/Division: Corporate/Murray Hill Relocation: No Posted Date: 1/9/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Essential Job Functions: performed in coordination with Assistant General Counsels with responsibility for other business units: * Participating in the continued development and implementation of Bard’s Compliance Program * Monitoring compliance trends and sharing best practices * Providing advice, on an on-going basis, to business personnel on compliance matters in connection with the day-to-day operation of the company’s business * Developing, implementing and presenting division and function-specific training programs (including developing training content internally, working with third-party vendors, and presenting and implementing training programs) * Developing and implementing auditing and monitoring programs to evaluate the company’s compliance with applicable laws, regulations and company policies (includes working with third-party vendors as needed to develop such programs) * Drafting company policies * Participating in and managing investigations (including oversight of outside counsel, if required), and preparing investigation reports * Supporting maintenance of database of compliance-related investigations * Reviewing education and research grant proposals, charitable contributions and sponsorships * Reviewing corporate copy and advertising copy Basic Qualifications: • Graduate degree, MBA or Law degree strongly preferred • 5+ years legal/compliance background in healthcare compliance, preferably within medical division or pharma company • Proven record of accomplishment in the areas of compliance policies, training, auditing, monitoring and investigations Additional Desirable Qualifications Skills and Knowledge: * Ability to work effectively with business personnel at all levels * Ability to work independently, but also accept direction from Chief Compliance Officer, and/or Associate General Counsel * Excellent interpersonal skills with the ability to relate easily with all levels within the organization * Collegial style, team player * Excellent oral and written communications skills Excellent analytical abilities2012-01-09 21:15:34United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ25783080http://crbard.jobs/xml/25783080/jobUSADelranQuality Engineer Industry Title /Category: Quality Engineer Job ID: 2011-5320 Career Level: entry level Location/Division: Davol/Delran Relocation: No Posted Date: 11/30/2011 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Summary of Position with General Responsibilities: Summary of Position with General Responsibilities: This position is responsible for the development and documentation of Quality Systems, as required, to support supplier quality objectives. This position will act as the quality representative regarding quality interests and concerns on manufacturing project teams as well as getting involved in a variety of projects which may include, resolving quality problems, improving areas of high quality costs, assisting suppliers and subcontractors in meeting Davol's quality needs. Essential Job Functions: * Plan and develop the Quality Control Program for various projects often within the context of a manufacturing project team. * Perform qualification studies for new suppliers, components, and inspection test equipment. * Provide technical support to resolve quality problems in manufacturing or with suppliers as warranted. * Design and conduct Quality Engineering studies to determine causes of quality non-conformances, initiate changes in process, tooling, product design, etc. to correct them. * Organize and generate detailed quality information reports to Engineering, Manufacturing, and Management. * Provide documented instructions for performance of Q.C. Inspections, including Inspection plans, Test Procedures, and Quality Standards. * Evaluate customer's specifications for Davol's ability to comply. * Plan and coordinate quality activities that involve Production, Planning, Inventory & Control, Engineering, etc. * Support the goals of the Quality Control Dept. and Profit Improvement Projects. Contribute ideas to these programs and work on implementation. Serve on committees, teams, task forces as assigned. * Conduct other Quality Control Projects as assigned by the Quality Control Manager * Exercise control over the quality of conformance of the products generated in areas assigned. * Facilitates the Material Review Notice (MRN) and Temporary Document Change System (TDCS) programs. This includes maintaining database and reporting to management. * Reviews DHR documentation for compliance and release of components and finished product. * Oversees the calibration program. This includes approval of new vendors, review of test results, and monitoring for compliance. * Responsible for coordination activities related to the Complaint review process and maintaining reporting programs to inform management * Serve on the Material Review Board (MRB). This includes providing leadership and coordination of activities for the investigation and disposition of non-conforming product and/or components. Basic Qualifications: ? A high level of competence in Quality Technology including statistical techniques, control charts, sampling plans, Quality costs, design of experiments, correlation and regression, analysis of variance, probability, etc. ? ASQ Certified Quality Engineer or equivalence ? ASQ Certified Quality Auditor or equivalent ? Experience with Statistical software and MS project software ? Good oral and written communication skills. ? Ability to work with and motivate people. ? Understanding of GMP, QSR, and other applicable regulations, and the ability to interpret these as they apply to company issues ? Good project planning skills and focused on meeting customer needs. ? Proven leadership skills in a facts pace environment Additional Desirable Qualifications Skills and Knowledge: Additional Desirable Qualifications Skills and Knowledge: * Experience in medical device Class II/III environment preferred Education and/or Experience: * Bachelor Degree in Mechanical/ Engineering or Technical Sciences * 3-5 years’ experience in quality technology or engineering, .2011-11-30 20:23:55United StatesC. R. BardNew JerseyNoneNJDelran, NJ25113253http://crbard.jobs/xml/25113253/jobUSAMurray HillSr. Supply Chain Analyst Industry Title /Category: Supply Chain Analyst Job ID: 2011-5282 Career Level: experienced Location/Division: LAPAC/Murray Hill Relocation: No Posted Date: 2/13/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Overview: Work independently or under little supervision to perform Supply Chain activities for assigned product portfolio to achieve customer service and financial goals in a global supply chain context. This includes demand forecasting, supply planning, inventory control, and monitoring and reporting of results. Summary of Position with General Responsibilities: Develop full understanding of product portfolio including medical usage, competitive positioning, and manufacturing processes. Monitor and maintain supply chain performance against customer service and financial goals Manage regional demand planning for assigned portfolio Support core SCM functions including SIOP, Inventory Planning, and Annual Budget Planning Develop working knowledge of Bard regulatory and quality systems and change control process Serve as primary contact for product supply for assigned geographic regions Lead planning aspects of new product launches during pre and post-launch phases Identify SKU rationalization and other lifecycle management opportunities Develop and maintain inventory strategies including inventory optimization and scrap reduction Leverage Lean and Six Sigma concepts to develop and effectively implement advanced Supply Chain solutions and process improvements Perform quantitative analysis of demand, supply and inventory issues Collaborate and problem-solve cross-functionally with internal business partners Develop decision support tools leveraging enterprise and desktop applications Track and report performance metrics Prepare executive-level presentations Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance. Education and/or Experience: EDUCATION and EXPERIENCE: * Undergraduate degree in quantitative discipline with minimum 3-5 years of related experience in supply chain or distribution role; MBA/MS preferred; or equivalent combination of education and experience. * Must have 2 years experience in healthcare industry with demonstrated understanding of product supply, distribution, quality management systems, and healthcare regulatory practices. * Must have strong analytical skills with the ability to work effectively and implement solutions in a cross-functional and multi-cultural environment. International experience preferred. * Must demonstrate strong verbal and written communication, interpersonal, and presentation skills; foreign language skills preferred. * Must be proficient in enterprise applications (ERP, APS, BI or ETL) and all Microsoft Office applications including advanced modeling in Excel and Access. * Must be able to maintain flexible work hours. Ability to travel domestically or internationally up to 10% is required.2011-11-04 19:02:57United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ24691464http://crbard.jobs/xml/24691464/jobUSAMurray HillERP Programmer/Analyst Industry Title /Category: ERP Programmer/Analyst Job ID: 2011-5259 Career Level: experienced Location/Division: Murray Hill/Corporate Relocation: No Posted Date: 11/3/2011 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Summary of Position with General Responsibilities: Must develop and support applications software for all users of Bard PeopleSoft Human Capital Management (HCM) Systems, develop project functional requirements, analyze, design, build, test, document, implement reports and interfaces using People Tools, such as Application Designer, Application Engine, Component Interface, PeopleCode , SQR and Crystal, apply PeopleSoft tax updates, patches, and bundles, maintain/develop UNIX scripts, and administer PeopleSoft application, web, and process scheduler servers. Education and/or Experience: Must have a minimum 5 years (collectively) of direct application development experience in (i) PeopleSoft (HCM) and (ii) Oracle Database. Of experience required, must have at least 3 years (concurrent) experience with PeopleSoft HR, Benefits and Payroll Applications version 8.9 or higher and 3 years (concurrent) of PeopleSoft Tools version 8.47 or higher. Must also have minimum 2 life-cycle PeopleSoft HCM implementation/upgrade experience. Relocation is not being offered with this position. BS in Computer Science or related field.2011-11-03 22:02:21United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ24577702http://crbard.jobs/xml/24577702/jobUSAMurray HillSenior Quality and Regulatory Systems Auditor Industry Title /Category: Medical Device/ Regulatory Job ID: 2011-5004 Career Level: experienced Location/Division: Murray Hill, NJ/ Corporate Relocation: Yes Posted Date: 5/13/2011 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare. We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded. Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world. Apply for this position * Refer a friend to this job More information about this job: Summary of Position with General Responsibilities: The Senior Quality and Regulatory Systems Auditor is responsible for implementing quality and regulatory audits of C.R. Bard and supplier facilities and products and for providing training and guidance for corporate and internal auditors. In this role, he/she assists the Director, Corporate Regulatory and Quality Audit with the planning of required annual audits and other audits as needed and assigned. He/she conducts in depth audits of quality and regulatory activities for compliance with applicable regulatory standards and functions as a subject matter expert for quality and regulatory issues. He/she provides leadership to the corporate audit team and Divisional/site internal auditors as needed in the conduct of audits, documentation of findings, support for auditee development of audit action plans and evaluation of effectiveness checks. He/she assures high quality reporting of audit findings and interfaces with division and manufacturing facility management to promote effective auditee corrective action plans. Essential Job Functions: 1. Provides leadership to the corporate audit team for the implementation of regulatory, quality (including design control) and quality system effectiveness audits of divisions, plants and suppliers by functioning as audit team leader. 2. Conducts routine and directed audits as assigned to assure compliance with FDA regulations, international standards and requirements, local SOP’s and corporate standards. 3. Provides guidance and coaching for corporate auditors in the conduct of audits, documentation of findings, support for auditee development of audit action plans and evaluation of effectiveness checks. 4. Acts as a subject matter expert for quality and regulatory audits and, as such, maintains a comprehensive knowledge of FDA quality and regulatory requirements and their interpretation, along with knowledge of international standards and requirements. 5. Provides guidance and direction to division and manufacturing facilities in the development of corrective action plans including corrections, corrective actions, preventive actions and effectiveness checks to address corporate audit findings. 6. Maintains a high degree of personal professional development through a combination internal and external training and participation in professional associations as appropriate. 7. Assists his/her management in optimizing resource utilization in the development of audit plans and implementation of audit schedules. 8. Provides support to management in the development of formal auditor training programs for corporate, division and plant internal auditors. 9. Provides auditor training to corporate audit staff, internal auditors and supporting auditors as assigned through formal classroom training, web based or on-the-job training. 10. Supports his/her manager in the development of quarterly and annual audit metrics and summaries for distribution to key division and manufacturing management. 11. Support management development of Corporate Policies, Standards procedures and guidelines as assigned to support the corporate audit program. 12. Maintains corporate audit files to assure conformance with applicable regulatory requirements. Basic Qualifications: B.S. degree in Engineering or the Physical or Biological Sciences 6+ years auditing of quality and regulatory systems for medical device manufacturers Knowledge of FDA quality systems regulations for medical devices Effective verbal and written communications at all levels of management Additional Desirable Qualifications Skills and Knowledge: Knowledge of FDA regulatory requirements for pharmaceuticals and combination products Certified Quality Auditor/ISO lead Auditor Certified M.S. or PhD in Engineering or the Physical or Biological Sciences Experience/working knowledge of design controls and regulatory systems as applied to medical devices Strong analytical skills and a high standard of judgment to identify significant quality and compliance issues Physical Demands: Incumbent must be physically able to travel domestically and internationally (Travel is 40% - 60%)2011-05-13 23:48:11United StatesC. R. BardNew JerseyNoneNJMurray Hill, NJ21274910http://crbard.jobs/xml/21274910/job