[{"country_short": "USA", "city": "Murray Hill", "description": "QA RA Associate\n\n\n\nIndustry Title\n/Category: Quality Assurance / Regulatory Affairs\nJob ID: 2012-5662\n\nCareer Level: experienced\nLocation/Division: International\n\nRelocation: No\nPosted Date: 5/21/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nThis 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.\n\n\nSummary of Position with General Responsibilities:\n\u2022 Coordinates full spectrum of complaint handling on behalf of Asia geographies.\n\u2022 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.\n\u2022 Wide interaction and communication with all Asia IBC\u2019s and Divisions to assist with entry and closure of complaints.\n\u2022 Prepare and maintain various complaint and MDR reports and metrics, and provide monthly summary on complaints by countries.\n\u2022 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.)\n\u2022 Assists the department head in other administrative duties (i.e. schedule meetings/travel supplies, etc.).\n\nEssential Job Functions:\n\nBasic Qualifications:\n* 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.\n* Strong interpersonal skills in the areas of verbal and written communication, telephone courtesy and professionalism.\n* Strong organizational skills and the ability to take initiative for assigned projects.\n* Attention to detail and the ability to maintain confidentiality of product registration documents.\n* Ability to prioritize and handle several projects concurrently.\n* Must be self-motivated and have ability to take ownership of her/his responsibilities.\n* Must be a team player and capable of working with minimal supervision.\n* Must be able to set goals and accomplish them within a set time schedule and budget.\nBasic Qualifications:\nEducation and/or Experience:\n\u2022 Two-year associate degree or equivalent.\n\u2022 Science major preferred.\n\u2022 Eight+ years minimum office administration/coordination experience in a fast paced environment.\n\u2022 Minimum three years experience working in a medical device-related environment required.", "date_new": "2012-05-21 19:29:35", "url": "http://crbard.jobs/xml/28835512/job", "country": "United States", "company": "C. R. Bard", "title": "QA RA Associate", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 28835512}, {"country_short": "USA", "city": "Murray Hill", "description": "ERP Programmer / Analyst\n\n\n\nIndustry Title\n/Category: ERP Programmer\nJob ID: 2012-5489\n\nCareer Level: experienced\nLocation/Division: Murray Hill\n\nRelocation: No\nPosted Date: 2/23/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nApplies 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.\n\n\nSummary of Position with General Responsibilities:\nEssential Job Functions:\n\u2022 Focused on ERP applications\n\u2022 Configures, analyzes, designs, develops, and maintains ERP program codes and applications to support business processes and functions\n\u2022 Performs all aspects of programming assignments and assists with system design\n\u2022 Develops project functional requirements\n\u2022 Finalizes project and system documentation\n\u2022 Monitors assigned projects to insure that predetermined deadlines are met\n\u2022 Tests all modules to ensure quality\n\u2022 Provides problem resolution for assigned software\n\u2022 Provides user assistance with assigned applications\n\u2022 Analyzes specifications for completeness and accuracy\n\u2022 Leads maintenance to existing applications\n\u2022 Adheres to ITS standards, policies and procedures\n\u2022 Provides technical support to teams\n\nEssential Job Functions:\n\nBasic Qualifications:\n* Strong JDEdwards E1development skills\n* Must have work experience with all facets of the JDE E1 Software Development toolset (OMW, ER, RDA, FDA, JDE C Business function, etc.).\n* Must be able to troubleshoot issues using various debug methods including debugging JDE C business functions.\n* Working knowledge of Order to Cash processes\n* Working knowledge of Oracle Database applications\n\nAdditional Desirable Qualifications Skills and Knowledge:\n* Ability to develop information solutions based on business requirements\n* Understand process and deliverables associated with each systems life cycle phases\n* Ability to determine balance between systems development and maintenance efforts\n* Knowledge of appropriate hardware and software required for application development\n* Knowledge of office productivity tools\n\n\nEducation and/or Experience:\n* Bachelor\u2019s Degree in Computer Science, Information Systems, or other related field. Or equivalent work experience\n* 3 to 5 years of IT work experience in programming and/or ERP systems analysis\n* Advanced programming techniques and software design\n* Knowledge of ERP applications or object oriented analysis and design", "date_new": "2012-04-11 12:36:37", "url": "http://crbard.jobs/xml/27814946/job", "country": "United States", "company": "C. R. Bard", "title": "ERP Programmer / Analyst", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 27814946}, {"country_short": "USA", "city": "Murray Hill", "description": "Clinical Research Associate II (CRA II)\n\n\n\nIndustry Title\n/Category: CRA\nJob ID: 2012-5516\n\nCareer Level: experienced\nLocation/Division: Murray Hill\n\nRelocation: No\nPosted Date: 3/7/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nMid-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\u2019s efforts towards continuous quality improvement.\n\nAbility to prioritze workload to meet study timelines while monitoring multiple protocols\n\u2022      Perform monitoring visits:\no Qualify potential investigative sites;\no Train and initiate investigative sites;\no Conduct routine monitoring visits and close out visits;\no Complete monitoring trip reports accurately inventoried and documented;\no Review case report forms to ensure data compliance;\no Account for investigational devices ensuring the devices are available, stored appropriately, and accurately inventoried and documented;\no Verify appropriate reporting and documentation of adverse events and protocol deviations per protocol requirements;\no Ensure site regulatory binder is current.\n\u2022      Manage investigative sites from study start up through close out:\no     Provide support to the investigator evaluation and recruitment process;\no     Assist in the collection of initial regulatory documentation;\no  Assist in the preparation of study binders, manuals, or other site specific tools.\n\u2022      Assist in the developmentof study specific monitoring tools.\n\u2022  Perform study tracking activities as requested.\n\u2022  Assists CRA Manager in development of Clinical Monitoring Plan.\n\u2022  Ability to work with little supervision\n\nSummary of Position with General Responsibilities:\nAbility to travel up to 50%.\n\nCertification (CCRA) through ACRP preferred, but not required\n\nBS / BA in a related scientific area;\n\u2022 Knowledge of clinical trial methodology relating to the monitoring of clinical trials, GCP, FDA, and / or country specific regulatory environment;\n\u2022      Minimum of 3 - 6 years of field monitoring experience;\n\u2022 Medical device experience preferred, but not required;\n\u2022 Proficient in MS Office Suite of products;\n\u2022      Experience with Clinical Trial Management System preferred;\n\u2022      Experience with EDC system preferred;\n\u2022 Excellent interpersonal and communication skills;\n\u2022      Proven ability to demonstrate strong decision making and problem solving skills.", "date_new": "2012-04-11 12:36:21", "url": "http://crbard.jobs/xml/27814933/job", "country": "United States", "company": "C. R. Bard", "title": "Clinical Research Associate II (CRA II)", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 27814933}, {"country_short": "USA", "city": "Murray Hill", "description": "Executive Assistant\n\n\n\nIndustry Title\n/Category: Executive Assistant\nJob ID: 2012-5553\n\nCareer Level: experienced\nLocation/Division: Murray Hill, New Jersey\n\nRelocation: No\nPosted Date: 3/29/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nSummary of Position with General Responsibilities:\nThis position is responsible for providing day-to-day administrative support to division Controller, Supply Chain Director and Customer Service Manager.\nEssential Job Functions:\n\u2022 General administrative duties such as typing, faxing, filing, Fedex/DHL mailings and mail distribution.\n\u2022 Heavy calendar management and international travel.\n\u2022 Coordinate complex, international travel arrangements and itineraries.\n\u2022 Organize meetings across multiple time zones.\n\u2022 Consolidate information for monthly reporting purposes.\n\u2022 Preparation and submission of expense reports and check requests.\n\u2022 Facilitate flow of documents that require signature.\n\u2022 Assist international staff with travel to Murray Hill office and other tasks as needed.\n\u2022 Assist in presentation preparations.\n\u2022 Flexible schedule required to meet demands of multiple international geographies.\n\u2022 Manage and maintain customer price files.\n\u2022 Maintain FCPA files and follow up to ensure records are complete and up-to-date.\n\u2022 Other duties as assigned.\n\nSummary of Position with General Responsibilities:\nBasic Qualifications:\n\u2022 Solid computer skills- Microsoft Word, Outlook, Excel and PowerPoint.\n\u2022 Minimum 5-7 years experience in an administrative role supporting multiple executives.\n\u2022 Prior experience supporting global executives.\n\u2022 Prior experience assisting a financial executive in a sales-based company.\n\u2022 Outstanding organizational skills.\n\u2022 Ability to manage confidential information.\n\u2022 Excellent oral and written communication skills.\n\u2022 Ability to manage and prioritize multiple tasks and deadlines.\n\u2022 Demonstrates initiative and is proactive.", "date_new": "2012-04-11 12:35:51", "url": "http://crbard.jobs/xml/27814890/job", "country": "United States", "company": "C. R. Bard", "title": "Executive Assistant", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 27814890}, {"country_short": "USA", "city": "Murray Hill", "description": "QualitySystems Engineer/Sr. Engineer\n\n\n\nIndustry Title\n/Category: Quality Systems Engineer\nJob ID: 2012-5475\n\nCareer Level: experienced\nLocation/Division: Murray Hill\n\nRelocation: No\nPosted Date: 2/15/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nSummary of Position with General Responsibilities:\nThe 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.\nEssential Job Functions:\n*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.\n*Prepare and assist in the reporting of the Management Review metrics to corporate executive management.\n*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.\n*Establish ownership of corporate quality information system(s) and provide guidance, assistance and training as a subject matter expert on same.\n*Compile, prepare and assist with the evaluation of Division recall plans when submitted for corporate review.\n*Write and approve validation protocols and reports including software validation.\n*Execute software/process validations.\n*Manage FDA inspection records.\n*Assists with Quality Systems or targeted Quality Audits.\n\nBasic Qualifications:\nBasic Qualifications:\n* Ability to understand and apply statistical and systems improvement tools to improve and sustain  the corporate quality system.\n*Knowledge of medical device regulation, industry or international standard, including management responsibility.\n*Project Management skills, including basic team leadership skills, and good organization skills\n\n\n*Ability to understand Corporate, Division and Plant Quality Systems and be able to implement systemic changes to enhance product quality and improve business efficiency.\n\u2022 Strong organizational, practical mathematical (statistical) skills, analytical and problem solving skills.\n\u2022 Strong communication, presentation, interpersonal, and organizational skills.\n\u2022 Ability to apply quality control theories and principles to an operational environment.\n\u2022 Six Sigma or Lean skills and tools exposure advantageous.\n\u2022 Computer literate; able to utilize MS Office Suite, MS Project various database platforms and custom applications software.\n\nAdditional Desirable Qualifications Skills and Knowledge:\n\nAdditional Desirable Qualifications Skills and Knowledge:\nASQ Certification (CQE, CRE, CQM etc.) a plus.\nEducation and/or Experience:\n\nBS Degree in Science, Engineering or equivalent.\nData management/analysis experience in the medical device or pharmaceutical industries is desired\n3+ years experience with Quality Assurance programs in a corporate environment preferred", "date_new": "2012-02-15 18:35:40", "url": "http://crbard.jobs/xml/26538095/job", "country": "United States", "company": "C. R. Bard", "title": "QualitySystems Engineer/Sr. Engineer", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 26538095}, {"country_short": "USA", "city": "Murray Hill", "description": "Senior Internal Auditor\n\n\n\nIndustry Title\n/Category: Medical Device/ Audit\nJob ID: 2012-5432\n\nCareer Level: experienced\nLocation/Division: Murray Hill, NJ/ Corporate\n\nRelocation: None Offered\nPosted Date: 2/28/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nThe 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.\n\nAs 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.\n\nOvernight travel (about 30-35%) is required to visit field locations. Approximately 75% of travel is domestic and 25% international is international, primarily in Europe.\n\nLong 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.\n\nSummary of Position with General Responsibilities:\nExcellent communication skills (both written and verbal)\n\u2022 Skilled at making presentations to Management and able to effectively sell ideas\n\u2022 Must be self motivated, have a passion for client service and strong desire to obtain new skills\n\n\u2022 BS/MS degree (must be eligible for CPA designation)\n- GPA of 3.0 or higher\n\u2022 MUST BE A Certified Public Accountant (CMA or MBA is a plus)\n\u2022 3-5 years experience in public accounting, big 4 Firms preferred.\n\u2022 Must be familiar with and able to accurately interpret U.S. GAAP.\n\u2022 Experience with manufacturing entities is strongly desired.\n\u2022 SEC client experience a plus.\n\u2022 Strong analytical skills required to gather, interpret and present findings.\n\u2022 Experience with Multi-location and international locations preferred.\n\u2022 Working knowledge of Sarbanes -Oxley and COSO requirements required.\n\n\nPhysical Demands:\n\n25%-35% - Travel", "date_new": "2012-02-06 20:20:15", "url": "http://crbard.jobs/xml/26338753/job", "country": "United States", "company": "C. R. Bard", "title": "Senior Internal Auditor", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 26338753}, {"country_short": "USA", "city": "Murray Hill", "description": "Assistant General Counsel - Compliance\n\n\n\nIndustry Title\n/Category: General Counsel\nJob ID: 2012-5399\n\nCareer Level: experienced\nLocation/Division: Corporate/Murray Hill\n\nRelocation: No\nPosted Date: 1/9/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nEssential Job Functions:\n\nperformed in coordination with Assistant General Counsels with responsibility for other business units:\n\n* Participating in the continued development and implementation of Bard\u2019s Compliance Program\n* Monitoring compliance trends and sharing best practices\n* Providing advice, on an on-going basis, to business personnel on compliance matters in connection with the day-to-day operation of the company\u2019s business\n* 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)\n* Developing and implementing auditing and monitoring programs to evaluate the company\u2019s compliance with applicable laws, regulations and company policies (includes working with third-party vendors as needed to develop such programs)\n* Drafting company policies\n* Participating in and managing investigations (including oversight of outside counsel, if required), and preparing investigation reports\n* Supporting maintenance of database of compliance-related investigations\n* Reviewing education and research grant proposals, charitable contributions and sponsorships\n* Reviewing corporate copy and advertising copy\nBasic Qualifications:\n\u2022 Graduate degree, MBA or Law degree strongly preferred\n\u2022 5+ years legal/compliance background in healthcare compliance, preferably within medical division or pharma company\n\u2022 Proven record of accomplishment in the areas of compliance policies, training, auditing, monitoring and investigations\n\nAdditional Desirable Qualifications Skills and Knowledge:\n\n* Ability to work effectively with business personnel at all levels\n* Ability to work independently, but also accept direction from Chief Compliance Officer, and/or Associate General Counsel\n* Excellent interpersonal skills with the ability to relate easily with all levels within the organization\n* Collegial style, team player\n* Excellent oral and written communications skills\nExcellent analytical abilities", "date_new": "2012-01-09 21:15:34", "url": "http://crbard.jobs/xml/25783080/job", "country": "United States", "company": "C. R. Bard", "title": "Assistant General Counsel - Compliance", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 25783080}, {"country_short": "USA", "city": "Murray Hill", "description": "Sr. Supply Chain Analyst\n\n\n\nIndustry Title\n/Category: Supply Chain Analyst\nJob ID: 2011-5282\n\nCareer Level: experienced\nLocation/Division: LAPAC/Murray Hill\n\nRelocation: No\nPosted Date: 2/13/2012\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nOverview:\nWork 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.\nSummary of Position with General Responsibilities:\nDevelop full understanding of product portfolio including medical usage, competitive positioning, and manufacturing processes.\nMonitor and maintain supply chain performance against customer service and financial goals\nManage regional demand planning for assigned portfolio\nSupport core SCM functions including SIOP, Inventory Planning, and Annual Budget Planning\nDevelop working knowledge of Bard regulatory and quality systems and change control process\nServe as primary contact for product supply for assigned geographic regions\nLead planning aspects of new product launches during pre and post-launch phases\nIdentify SKU rationalization and other lifecycle management opportunities\nDevelop and maintain inventory strategies including inventory optimization and scrap reduction\nLeverage Lean and Six Sigma concepts to develop and effectively implement advanced Supply Chain solutions and process improvements\nPerform quantitative analysis of demand, supply and inventory issues\nCollaborate and problem-solve cross-functionally with internal business partners\nDevelop decision support tools leveraging enterprise and desktop applications\nTrack and report performance metrics\nPrepare executive-level presentations\nEnsure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.\n\nEducation and/or Experience:\n\nEDUCATION and EXPERIENCE:\n* 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.\n* Must have 2 years experience in healthcare industry with demonstrated understanding of product supply, distribution, quality management systems, and healthcare regulatory practices.\n* 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.\n* Must demonstrate strong verbal and written communication, interpersonal, and presentation skills; foreign language skills preferred. \n* Must be proficient in enterprise applications (ERP, APS, BI or ETL) and all Microsoft Office applications including advanced modeling in Excel and Access. \n* Must be able to maintain flexible work hours. Ability to travel domestically or internationally up to 10% is required.", "date_new": "2011-11-04 19:02:57", "url": "http://crbard.jobs/xml/24691464/job", "country": "United States", "company": "C. R. Bard", "title": "Sr. Supply Chain Analyst", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 24691464}, {"country_short": "USA", "city": "Murray Hill", "description": "ERP Programmer/Analyst\n\n\n\nIndustry Title\n/Category: ERP Programmer/Analyst\nJob ID: 2011-5259\n\nCareer Level: experienced\nLocation/Division: Murray Hill/Corporate\n\nRelocation: No\nPosted Date: 11/3/2011\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nSummary of Position with General Responsibilities:\nMust 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.\nEducation and/or Experience:\n\nMust 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.\n\nBS in Computer Science or related field.", "date_new": "2011-11-03 22:02:21", "url": "http://crbard.jobs/xml/24577702/job", "country": "United States", "company": "C. R. Bard", "title": "ERP Programmer/Analyst", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 24577702}, {"country_short": "USA", "city": "Murray Hill", "description": "Senior Quality and Regulatory Systems Auditor\n\n\n\nIndustry Title\n/Category: Medical Device/ Regulatory\nJob ID: 2011-5004\n\nCareer Level: experienced\nLocation/Division: Murray Hill, NJ/ Corporate\n\nRelocation: Yes\nPosted Date: 5/13/2011\n\nClose Date: .. \nC. 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.\n\nWe expect the highest levels of quality, integrity, service, and innovation from our employees \u2013 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.\n\nBe Your Best at Bard \u2013 and ultimately, you can have an impact on the lives of people around the world.\n\nApply for this position\n* Refer a friend to this job\nMore information about this job:\nSummary of Position with General Responsibilities:\nThe 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.\nEssential Job Functions:\n\n1. 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.\n\n2. Conducts routine and directed audits as assigned to assure compliance with FDA regulations, international standards and requirements, local SOP\u2019s and corporate standards.\n\n3. 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.\n\n4. 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.\n\n5. 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.\n\n6. Maintains a high degree of personal professional development through a combination internal and external training and participation in professional associations as appropriate.\n\n7. Assists his/her management in optimizing resource utilization in the development of audit plans and implementation of audit schedules.\n\n8. Provides support to management in the development of formal auditor training programs for corporate, division and plant internal auditors.\n\n9. 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.\n\n10. Supports his/her manager in the development of quarterly and annual audit metrics and summaries for distribution to key division and manufacturing management.\n\n11. Support management development of Corporate Policies, Standards procedures and guidelines as assigned to support the corporate audit program.\n\n12. Maintains corporate audit files to assure conformance with applicable regulatory requirements.\nBasic Qualifications:\nB.S. degree in Engineering or the Physical or Biological Sciences\n6+ years auditing of quality and regulatory systems for medical device manufacturers\nKnowledge of FDA quality systems regulations for medical devices\nEffective verbal and written communications at all levels of management\n\nAdditional Desirable Qualifications Skills and Knowledge:\n\nKnowledge of FDA regulatory requirements for pharmaceuticals and combination products\nCertified Quality Auditor/ISO lead Auditor Certified\nM.S. or PhD in Engineering or the Physical or Biological Sciences\n\nExperience/working knowledge of design controls and regulatory systems as applied to medical devices\n\nStrong analytical skills and a high standard of judgment to identify significant quality and compliance issues\nPhysical Demands:\n\nIncumbent must be physically able to travel domestically and internationally\n(Travel is 40% - 60%)", "date_new": "2011-05-13 23:48:11", "url": "http://crbard.jobs/xml/21274910/job", "country": "United States", "company": "C. R. Bard", "title": "Senior Quality and Regulatory Systems Auditor", "reqid": null, "state": "New Jersey", "state_short": "NJ", "location": "Murray Hill, NJ", "uid": 21274910}]