LinkedIn Groups |
James Miller has started a discussion: Is Your Resume Preventing You From Getting a New Job? "Are your job expectations realistic that you can actually get the jobs you are applying for? Too many times people waste their own time applying for jobs that they are not suitable for. I recently worked with a young professional with 2 years of work experience and no managerial experience. http://thejobsadvisor.com/716.php" |
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We help the job seekers by providing opportunities available in various parts of the world. We scan various companies and consultant requirements and list their career requirements.
Wednesday, September 14, 2011
New discussion Is Your Resume Preventing You From Getting a New Job?
New job Senior Quality Systems Manager Consultant-Philadelphia Area
LinkedIn Following |
Robert Ciociola posted a job: Senior Quality Systems Manager Consultant-Philadelphia Area "Contract Position-Send resumes to bciociola@covexllc.com A Healthcare company in the Philadelphia area is in need of a Quality Systems Manager to assist with the roll out of eTQ NC CAP as well as MES Werum and SAP DESCRIPTION • Experience in the deployment and /or use of quality and enterprise systems. • Balance between planning from previous experiences and being able to roll up sleeves and help out when needed. • Experience with specific software tools SAP, Werum, ETQ/Trackwise and Documentum would be preferred. • Experience rolling out electronic batch records systems. • Experience working across sites with different processes, getting them aligned around common requirements and providing leadership and coaching on how to manage the associated change in culture and process • ETQ Project Management Resource will support any/all project implementation activities for ETQ • They may report directly the Director or his PM already on the project • Operational support will include: o ETQ post-go live operational needs (SOP revision, training material enhancement, training/re-training, post go-live system support) o ETQ enhancement (R6.1) project activities (scope to include FDA commitments and other ‘GMP’ issues) • Must be a solid hands on PM with Quality ETQ/Trackwise (NC-CAPA) project implementation experience • Will be a bridge between IT and The Quality systems organization COMPENSATION Competitive C2C rate" |
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New job Medical Device Auditor - Inspection and Certification Industry USA
LinkedIn Following |
Simon Harding posted a job: Medical Device Auditor - Inspection and Certification Industry USA "Job Country or Region:United States of America Medical Device Auditor - Inspection and Certification Industry Job Location:Indianapolis Discipline:Quality Management Created:13 September 2011 15:56:16 Company Description: Chronos Consulting (www.chronosconsulting.com) is part of the Coberon Chronos Group, an award winning global leader in permanent and temporary staffing, RPO and business process automation solutions (www.chronosworkflow.com) for global multinationals. The Group owns and operates 41 offices worldwide. Chronos Consulting's client is a global leader in inspection and testing services with over 60,000 + employees. They provide certifications enabling clients to demonstrate regulatory compliance with the appropriate medical device regulations, as well as improve quality management systems and processes. An exciting opportunity for an Auditing or QA Medical Device professional to work with an inspection and certification industry leader. This is a salaried, home base role with extensive travel and opportunities for growth within the company. Tailored auditing training will be provided for more junior applicants. Job Description Home base role with client site travel (ideally living close to a major airport hub). The Role: Reporting to the Operations Manager, you would be responsible for: Performing 3rd party audits per company’s procedures and the requirements of the applicable standard and ISO 13485. Collecting and analyzing sufficient information to provide a recommendation for certification and deciding, upon evidence gained, whether or not registration should be recommended or allowed to continue. Traveling and working on-site at different locations based on client needs - you must be flexible and open to extensive travel Assisting in the training of other auditors during planned audits or other training opportunities. Job Qualifications The Requirements: B.A. Degree in Engineering or the Sciences a plus. 2 - 5 + years of experience in a QA or auditing role within a Medical Device environment. Competent working knowledge of nationally recognized Quality auditing standards and procedures. Ability to travel and located within close proximity to an airport. Medical Device Auditor - Inspection and Certification Industry Strong communication and presentation skills coupled with integrity, tact, and character. Completion of RAB/QSA or IRCA approved training course in Quality, not required, but would be an asset. APPLY usa@chronosconsulting.com" |
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