At Bureau Veritas, our most valuable resource is our people.

Bureau Veritas Consumer Product Services, Inc. (BVCPS) is a leading quality assurance service provider to the consumer product and retail markets with expertise in testing, consulting, training, inspection, auditing and social accountability.

BVCPS offers over 60 offices and laboratories in 40 countries with 5,000 employees and a global network of quality assurance services supported by 600 Bureau Veritas offices in 140 countries with a workforce of more than 20,000 employees.

DescriptionRsponsibilities will include but are not limited to sample preparation and analysis of various samplematrices by X-ray diffraction, data review with senior analyst oversight, write and review StandardOperating and Specific Task procedures.

Required SkillsTime management, good organization, strong verbal and written skills, ability to workindependently and in a team environment, capable of making sound decisions quicklyand efficiently, ability to handle mutiple projects, and knowledge of Microsoft Excel, Work, and Access.

Knowledge of and coursework in Geology is a plus.We offer an attractive salary/benefit package and an opportunity to play a vital role with a dynamic organization.For more information and to apply online, please visit our website at: http://hostedjobs.

openhire.com/epostings/jobs/submit.cfm?fuseaction=dspjob&jobid=202216&company_id=15890&jobboardid=24 LOCAL CANDIDATES ONLY – NO RELOCATION ASSISTANCE PROVIDED FOR THIS POSITION.

EOE M/F/D/V

Laboratory Analyst (1214) Job in Novi

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The selected candidate will be responsible for creation and maintenance of queries and reports to support the data requirements of the S2 LOB as well as ongoing support to users of self service reporting solutions.

Provide demonstration support for audits as well as testing support for upgrade, integration, and process improvements efforts.

Ensure a high level of data quality through ongoing self audit of reporting quality.

Perform day-to-day responsibilities with a strong customer service focus and sense of urgency.

Responsibilities: – Perform day-to-day reporting tasks and customer support for the S2 LOB. Work with customer to translate customer needs to a defined set of reporting requirements.

Strong attention to self audit and constant evaluation of reporting quality.

- Work with and understand data across a variety of applications: Peoplesoft HR, Deltek, HodesIQ, SumTotal Systems (L&D), Berkshire, etc. and how the data relates across the applications.

- Partner with functional HR counterparts to deliver effective support, solutions, and services to the broader LOB.- Establish and maintain relationships and effectively interact across the LOB to analyze reporting needs and formulate working solutions.

Possess strong customer service focus; demonstrated ability to understand the customer’s business, issues, and needs, proactively respond to customer requirements.

Maintain clear communication and take action to continuously enhance the customer experience.

- Perform activities with a constant attention to areas where process improvements and automation can increase data integrity, standardize solutions across the LoBs, decrease manual workload, and enhance the delivery to the customer.

Effectively communicate areas targeted for improvement and proposed solutions.

- Provide functional support for process improvements activities, upgrades, integrations, and reorganizations.

Participate in testing and feedback process.

- Provide support for internal and external audits.

- Actively seek to understand needs of business and balance such requests with trend toward consistency across the enterprise in delivering effective HRIS solutions and services.

Must have: High school diploma and 6 years related experience OR Associate degree and 4 years related experience OR Bachelor’s degree and 2 years related experience Ability to communicate effectively, both orally and in writing Developed communication skills to exchange complex informationSound interpersonal skills Ability to utilize computer skills to prepare appropriate reports and documents Strong organizational and analytical skills and demonstrated track record for results Demonstrated responsiveness and sense of urgency with customer requests and project schedules Fundamental understanding and experience with HR systems and processes Fundamental understanding of how to utilize technology as an enabler Ability to make decisions using sound judgment while complying with policies, procedures, appropriate principles, and applicable state and federal laws and regulations Ability to select appropriate alternative sources of information and utilizes them to evaluate situationswhich have a direct impact on quality and timeliness of data delivered across the organization Ability to negotiate, mainly internally within a project team or department.

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 105,000 employees worldwide, BAE Systems had 2008 sales of $34.

4 billion.

Support Solutions, based in Rockville, Maryland, provides a wide range of services in engineering, system integration, ship repair, and readiness and sustainment for military platforms.

Its Technology Solutions & Services unit addresses the full life-cycle needs of US Department of Defense and federal civilian customers with capabilities in systems engineering and technical assistance, system and subsystem integration, operations, and maintenance.

TSS serves every branch of the US military and numerous civilian agencies, operating the US Army’s munitions plant in Kingsport, Tennessee; integrating communications systems and developing and integrating precision tracking radars; and providing design and support services for air and missile defense systems.

The Ship Repair business is the leading US provider of non-nuclear ship repair, conversion, and modernization services.

It focuses on drydock and pier-side ship repair and sustainment services for the US Navy, other defense agencies, and commercial customers.

The Readiness & Sustainment business focuses on customers’ growing need for through-life platform support.

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.

Join us .

To Apply for this position, please CLICK HERE


HRIS Analyst Job in Rockville 20847, Maryland US

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For more than 100 years, Chicago-based USG has been a leader in producing innovative products and systems to build the environments in which we live, work and play.

As the inventor of wallboard and mineral wool ceiling tile, USG created North America’s building materials industry.

Our products are used in everything from major commercial developments and residential housing to simple home improvements.

Our flagship brands include SHEETROCK® Brand gypsum panels and DUROCK® cement board, which are recognized around the world.USG is North America’s leading producer of gypsum wallboard, joint compound and a vast array of related products for the construction and remodeling industries.

We are also the global leader in the manufacture of ceiling suspension systems and are recognized as the premier acoustical panel and specialty ceiling systems innovator.

Our family of products provides creative building solutions that set new standards for productivity and efficiency, helping contractors and architects deliver high quality and innovative designs.

USG, through its subsidiary L&W Supply, is also the nation’s largest distributor of drywall and related building products.

L&W serves the professional contractor through a network of nearly 200 locations and strives to be their preferred source for all quality products and services they need to complete their projects on time and on budget.Our steadfast commitment to the company’s core business beliefs – safety, integrity, service, innovation, diversity, efficiency and quality – have helped us become the industry leading company we are today.

USG’s 12,700 employees working in more than 30 countries are dedicated to helping our customers and partners achieve success.

We are committed to the highest levels of customer satisfaction and quality in everything we do.USG currently has an opening for a Technical Specialist based in our corporate office in downtown Chicago.Job Description

1. Designs, configures, develops, tests, installs, monitors and maintains software, hardware, databases, desktop operating systems, and various technical tools2.

Monitors systems and adjusts performance to keep system functioning properly and downtime to a minimum3.

Customizes systems by modifying, and testing modifications, to adapt to new functions4.

Develop and execute test/validation scripts with expected results; perform results analysis and identify design changes based upon testing results5.

Reviews and prepares documentation for new and modified systems, environments, hardware, software, or databasesJob Requirements

1. Bachelor’s Degree in Computer Science or related field desired2.

A minimum of 5 years of technical experience in a given area (mainframe, network, PC, telecommunications, data management)3.

Ability to work indepedently with limited supervision4.

Strong analytical and problem solving skills.

Excellent communication skills and development of documentation (document processes and standards, support training materials, etc.)5. Primary work location is Corporate Headquarters, but will also be required to work at the USG Customer Service Center in Schiller Park and the Corporate Innovation Center in Libertyville IL on an as needed basis.

May be required to provide 24 hour on call support USG offers a comprehensive benefits package that includes medical, dental, vision, and life insurance; retirement and investment plans; paid holidays and vacations; tuition reimbursement.

Relocation is not provided.

To learn more about USG Corporation, check out our web site at www.usg.com. Candidates must be authorized to work in the United States.

USG Corporation is an Equal Opportunity Employer M/F/D/V.


IT Technical Specialist – USG Corporation Job in Chicago, Illinois US

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Primary Role: The Senior SAS programmer will be responsible for developing and designing SAS programs that access, prepare, analyze, and report clinical trial data.

Responsibilities: Responsibilities for the Senior SAS Programmer include but are not limited to

1. Development, maintenances, and production of data listing, summary, validation, and analysis programs that meet specifications described in trial documentation (50%).

2. Use, modify and maintain existing SAS program code as necessary (5%).

3. Participate in and/or lead process/quality improvement initiatives (20%).

4. Work with database managers in the standardization of database design and validation (10%).

5. Effectively communicate status updates to project team members and department leaders in a timely manner (5%).

6. Review and provide programming input to Protocols, Database Specifications, Data Validation Specifications, Statistical Analysis Plan and other study related documentations (5%).

7. Provide leadership and mentoring to less experienced programmers (5%).

8. Ensure all work is processed on time to appropriate quality levels.

Shire is committed to providing high quality, competitive, and appropriate health care benefits for employees and their families.

Shire is an Equal Employment Opportunity and Affirmative Action Employer.

Requirements: Education & Experience Requirements: A qualified Senior SAS Programmer will have: Bachelors degree in math, statistics, computer science or other related field with at least 6 years in industry related (Pharmaceutical, Biotech, CRO) SAS programming experience; or Masters degree in math, statistics, computer science with at least 3 years in industry related SAS programming experience.

Key Skills and Competencies: Specific Skills

1. Expert knowledge of clinical trials and experience of using SAS to analyze and report the results of clinical trials.

2. High level of analytical skills in programming using BASE/SAS, SAS/STAT, SAS MACROS, and SAS/GRAPH.

3. High level of experience in constructing technical programming specifications and producing validated SAS programs.

4. Demonstrated written and oral presentation skills and ability to communicate effectively to other programmers and non-technical colleagues.

5. Ability to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environment.

6. Demonstrated ability to work in global teams as well as manage projects independently.

7. Detail oriented and pursuing accuracy and thoroughness.

8. Self improvement mentality with positive attitude.

Apply to Shire


Senior Programmer Job in Lexington 02142, Massachusetts US

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We are now hiring and training the Managers who will become our Stores Managers and District Managers in the near future.

Just as we offer our customers the widest range of quality housewares and home furnishings, we offer energetic and ambitious individuals a wide range of outstanding opportunities, an incredible sense of loyalty, and the ability to grow with a proven leader.

We offer competitive salaries and a comprehensive benefit package.

POSITIONS AVAILABLERequirements: Successful candidates with retail management experience – Department Manager, Store Manager, District Manager or any level in between – will be given the opportunity for unlimited advancement via our “promote from within” program.


Store Management Job in Santa Fe

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Job Summary: Test fixes and enhancements for in-house software applications.

Create and maintain software applications enhancing corporate competitiveness.

Perform all duties assigned by the Team Lead.

Must know, practice and ensure that company policies and procedures and state and federal laws are followed at all times.

Ensure that no company, employee or customer information is inappropriately divulged to unauthorized parties.

Responsibilities and Duties

1.  Perform in cross functional and matrixed teams; work with Programmer Analysts to troubleshoot issues that arise with testing applications and work with Business Analysts to comprehend business user functional process.

2. Prepare and execute test plans for functional areas of applications.

Perform automated and manual testing and document test failures.

Develop new scripts and regularly review testing requirements and automated scripts generated.

Create and execute test scripts.

3. Evaluate and test new or modified applications, components, documentation, diagrams and flowcharts prior to release4 Write and revise testing standards and procedures to continually improve the quality of projects implemented5 Maintain a repository of all quality records such as defects, issues, review findings and improvement opportunities6 Verify that applications meet end user requirements as well as technical production requirements7 Identify problems and recommend enterprise wide solutions and improvements for complex and high risk projects.

Analyze performance data and provide management reports on the effectiveness of the Quality Assurance system8 Maintain positive employee relations and morale whenever possible.

Practice sound leadership and human relations principles to promote teamwork at all times.

Set a good personal example of attitude and performance.

Resolve employee relations problems, complaints, suggestions, etc. Follow-through and communicate employee relations problems to the Team Lead.Job Qualifications: Education: Associates Degree or equivalent experience required.

Experience: One (1) year experience in manual software testing in a client server or web based environment or similar experience utilizing one or more of the following technologies required: Oracle Forms, Visual Basic, Java, .

Net, PowerBuilder and SQL. Three (3) or more years experience in an IT or business setting required.

Familiar with software testing concepts, practices and procedures.

Bilingual abilities a plus.

      ADESA offers a comprehensive compensation package including, paid vacation, medical, dental and vision insurance, tuition reimbursement and 401K.

Equal Opportunity Employer (M/F/D/V)


Software Quality Analyst Job in Carmel 46032, Indiana US

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Dont find a sales job, find a sales career.

Combined Insurance is looking for quality individuals to join it’s sales team.

We provide training, a completetion bonus, comprehensive benefits and leads for your local market.

Call ODelia Ross 859-221-6469.

This listing brought to you by The Times – Tribune


Sales Job in 40701

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Billerica, MA Corporate HeadquartersPosition Summary:  Millipore Corporation strives to provide manufacturing bioprocess solutions to the biotech industry.

 A Millipore solution is a unique, comprehensive, and validated combination of products, services, and applications expertise for API and drug product manufacturing.

 The Senior QE would be responsible for providing quality assurance (specifically design assurance and quality by design, QbD) support for the development of new Millipore products and solutions pertaining to monoclonal antibody processing, cell culture/fermentation/harvesting, vaccine processing, purification, filtration, disposable processing, PAT This position reports to the Manager of Quality Engineering (BioProcess).

  Primary Responsibilities: Provide expert design assurance guidance and support for Millipore product, program, and solution development projects.

 Responsibilities to include: Quality by DesignDesign controlProduct and process validationcGMPRisk management Interface and coordinate activities with other quality functions including manufacturing site quality, quality systems, regulatory affairs, external quality groups, etcInterface with and leverage the entire matrix organization at Millipore in order to best achieve organizational goals.

Lead and support continuous improvement activities.

Education & Experience Requirements: 7-10+ years progressive, seasoned design assurance engineering within the pharmaceutical or biotech industriesExtensive validation experience within the pharmaceutical or biotech industriesMinimum – bachelors degree in related technical area (engineering, chemistry, microbiology, etc)Knowledge of domestic and international quality and regulatory requirements (ICH and CFR), including current industry interpretation.

 Hands on experience in the application of quality system standards Experienced at working in cross-functional international teams.

Other necessary expertise: Sterile processingContamination controlQuality control and testingFailure analysis and problem solvingContinuous improvementDevelopment of solutions to complex problemsWorking predominantly without direction, exercising considerable latitude in determining objectives and approachesCompetencies Required: High level of emotional intelligenceProject leadership Certified Quality EngineerSix Sigma CertificationApplied/industrial statisticsProject managementMust be able to multi-task and prioritize activitiesTechnical, scientific backgroundStrong written and verbal communication skills (internal/external)Relationship builder, cross-functional partnershipResiliency, flexibilityBroad global perspective cross cultural awareness and sensitivityStrong organizational skillsWillingness and ability to travel internationally to Millipore, vendor, partner, and customer locations  Sterile processingContamination controlQuality control and testingFailure analysis and problem solvingContinuous improvementDevelopment of solutions to complex problemsWorking predominantly without direction, exercising considerable latitude in determining objectives and approachesCompetencies Required: High level of emotional intelligenceProject leadership Certified Quality EngineerSix Sigma CertificationApplied/industrial statisticsProject managementMust be able to multi-task and prioritize activitiesTechnical, scientific backgroundStrong written and verbal communication skills (internal/external)Relationship builder, cross-functional partnershipResiliency, flexibilityBroad global perspective cross cultural awareness and sensitivityStrong organizational skillsWillingness and ability to travel internationally to Millipore, vendor, partner, and customer locations


Design Assurance Engineer Job in Billerica 01821, Massachusetts US

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The Company Seniorlink, Inc. (the parent company of Caregiver Homes and Seniorlink Care) is a fast growing organization dedicated to making a difference in the lives of frail elders and developmentally disabled adults.

Our mission is to help seniors age with dignity by enabling them to live in the least restrictive setting possible.

By providing community choice and avoiding nursing home placement, we save millions of dollars over more costly institutional placement.

We aim to make a measureable difference in the lives of our clients and caregivers through delivery of expert, state-of-the-art in-home services.

We are currently developing our third generation of web based case management software to support our activities; resulting in opportunities to enhance the lives of our clients, and to contribute to the field of scholarly research and reporting.

The Career Opportunity We are looking for a Corporate Compliance Specialist with experience in the healthcare arena.

Youll be part of Seniorlinks new Center for Clinical Excellence.

The Center focuses on Quality Management initiatives across the Seniorlink continuum of services and programs, and includes Quality Assurance, Quality Improvement and Corporate Compliance.

Additionally, the Center analyzes clinical and outcome data fueled in part by Compliance initiatives to create information helpful in improving and standardizing our service delivery programming.

This is a unique opportunity to get in on the ground floor to create a role that is relevant and which meaningfully contributes to Seniorlinks success.

If you have ever envisioned working for a dynamic, growing company that is outcome and quality driven, wants to use data and information to effect positive change, and is nimble enough to make decisions in one meeting, then Seniorlink is for you! The Job Opportunity Under the direction of the VP for Clinical Excellence, the Corporate Compliance Specialist will integrate corporate programs related to the Ethics & Governance, HIPAA, Medicaid billing, Records Retention and other related clinical and regulatory imperatives.

The successful candidate will present all necessary information and actions to ensure achievement of the objectives of an effective compliance program including audits, training, in-house consulting, and investigation and resolution.

We are looking for someone who is experienced in corporate compliance in a healthcare services environment.

The Specialist will quickly become a valued part of our Quality Management program; contributing data and insights to our growing network of providers.

Specific responsibilities and expectations: Be expert: Provide written and oral advice and guidance regarding compliance requirements clinical and regulatory – that impact on Seniorlinks services and business; Stay Current: Analyze new and proposed legislation that impacts company operations, products, services, or distribution channels, and initiate appropriate action; Investigate and Report: Perform internal compliance investigations and audits throughout Seniorlink, including compiling detailed reports with recommendations to the Chief Compliance Officer and management; Create and Train: Develop compliance training materials and perform ongoing compliance training to Seniorlink employees, including the development of computer based training; Analyze process and quality: Provide ongoing advice and resources to management for compliance issues and process monitoring and improvement, and work with management to implement these improvements; Communicate, collaborate and manage: Assist the Chief Compliance Officer with the development and implementation of the annual Corporate Compliance Plan.

Participate as a compliance expert, as appropriate, in committees and groups established to support business initiatives or process modifications and oversee coordination of compliance implementation with other company departments and business units; Other duties as assigned: If you join the Seniorlink team, prepare to be nimble, be eager to take on new challenges and remain flexible! We are a vital, growing company that values creative thinkers and action oriented employees.

The Ideal Candidate · Compliance experience: we are seeking a trained compliance professional with 3-5 years of direct experience in a healthcare setting.

Greatly preferred: Bachelors degree in nursing (or other allied health field), health administration or related fields;· Compliance expertise: Health Care Compliance (CHC) certification (or certification eligible) by the Health Care Compliance Association, or similar experience and certification;· Demonstrated training skills: experience in the design and presentation of training programs based on an assessment of training needs;· Excellent organizational and time management skills you need to thrive in an active, high energy environment including the ability to juggle priorities and tasks with ease;· Excellent communication skills ability to effectively and efficiently exchange ideas, information and opinions with others and to arrive at decisions, conclusions or solutions;· Ability to travel to regional offices for training and investigations (approximately 10-30% of the time);· Technical skills: Seniorlink places great emphasis on core technical skills; we utilize the web for training, the Microsoft Office productivity suite, and any number of databases for mining and analysis.

Contact If you are interested in a rewarding career with Seniorlink, please email your cover letter and resume to: HR [at] seniorlink [dot] com Reference “Compliance Specialist” in the subject area.

Visit us at www.seniorlink.com. Seniorlink is an Equal Opportunity Employer.


Corporate Compliance Specialist Job in Boston 02116, Massachusetts US

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Objective of Position The QA Supervisor will be responsible for managing a team of quality assurance / quality control and compliance professionals in the development, implementation, and maintenance of quality assurance systems in support of our manufacturing facility at 250 Windy Point Drive, Glendale Heights, Illinois. Responsibility Responsibilities include nonconformance reporting, GMP / QSR investigations, corrective and preventive actions, GMP / QSR document changes, change control and performance metrics. Advising the staff on changes and their implementation and provides training tools and techniques to enable others to achieve Compliance. Knowledge of GMP / QSR regulations and interfacing with regulatory agencies is essential. Specific Duties Ã˜      Manage a team of quality professionals to achieve quality, compliance and business objectives.Ø      Analyze, develop and improve quality systems and associated business processes to achieve compliance with global regulatory requirements.Ø      Develop and maintain policies, standards, procedures, and guidelines encompassing all quality systems and facilitate deployment.Ø      Take a leadership role in quality programs and initiatives, make recommendations to continuously improve systems.Ø      Responsible to conduct internal compliance audits, manage timelines and schedules, generate audit reports, review audit responses and conduct follow – up to track resolution.Ø      Support investigation activities utilizing root cause and problem – solving methodologies as well as support CAPA development and implementation.Ø      Contribute to the design plan and execution of validation studies.Ø      Develop and maintain department and site metrics for monitoring critical process and quality attributes.Ø      Review and approve appropriate technical documentation in support of cross functional and cross departmental projects.Ø      Act as ISO Management RepresentativeØ      Perform other duties as assigned Shared Duties Ã˜      Support during project upgrades and modificationsØ      Implementation of corporate imageØ      Internal coordination tasks and activitiesØ      Manage client and regulatory auditsØ      OSHA regulation awarenessØ      Interactions with Manufacturing Operations, Process Engineering, Validation Services, External Vendors / Service Providers. Qualifications Ã˜      5 plus years of commensurate experience in quality assurance (QA) with increasing responsibilities, within the pharmaceutical / medical device industry.Ø      2 plus years if experience as a manager or in a leadership role within the QA organization in pharmaceutical / medical device industry preferably in an aseptic manufacturing environment.Ø      In-depth working knowledge of cGMP, QSR, 21 CFR, ISO 13485, ISO 9001, ICH and all other applicable international regulations, standards, Directives and Guidance.Ø      In-depth knowledge of developing and deploying quality systems within pharmaceutical / medical device industry.Ø      Strong analytical skills with proficiency in the application of problem-solving and root cause analysis methodologies.Ø      Strong verbal and written communication skillsØ      Strong managerial skills and a team player.Ø      Ability to multi-task and manage priorities.Ø      Ability to interface at all technical levels.  Medefil, Inc. is one of the leading manufacturers of pre-filled syringes in USA. This is a highly visible position with responsibility for leading and directing a team. Medefil offers attractive salary, strong benefits including 401(k) and career growth.


QA Supervisor Job in Glendale Heights 60139, Illinois US

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