Job Title: CAAR621726 - Manager, Quality Assurance
Company: Holcim (US) Inc.
Location: Dundee, MI
Description:
Manager, Quality Assurance Dundee, MI Holcim (US) Inc., one of the nation's largest manufacturers and distributors of cement and mineral components, has an immediate opening in our Dundee, Michigan office for a Manager of Quality Assurance. You will become a member of the Quality team and report to the Vice President of Quality and Product Performance. With will be responsible for the following: · Manage the Holcim US Quality program by ensuring that all parts of the program are in place and working · Work with plant Quality Control Managers in ensuring compliance with all external and internal quality objectives· Ensure tests and procedures are properly understood, carried out, and evaluated· Assist in training and development of plant Quality Control Managers· Identify relevant quality-related training needs and support training for all plant Quality Control Managers, as needed· Develop and issue quality reports· Assist the plants in solving product issues and developing new products · Participate in designated Quality Councils and Quality Council meetings · Actively participate in outside associations such as ASTM to support Holcim initiatives· Manage the Holly Hill Concrete Lab· Ensure that quality information systems (LDMS, CTRS, TIS) are up to date and useful to the Quality Control Managers and Technical Service Engineers; maintain quality-related master data in SAP· Ensure that all quality-related documents (i.e., mill certificates, quality objectives, etc.) are accurate and up to date· Travel 30-40% of the time The ideal candidate for the Manager of Quality Assurance would have bachelor’s degree in Engineering, Chemistry or Geology or a related field, advanced degree preferred. They would at least ten years of related management experience in cement and concrete, they would have excellent communication skills, strong problem solving and analytical skills. In addition this position requires exceptional computers skills including Microsoft Office and experience with SAP. For more information or to apply please visit our website at http://www.holcim.us / and click on People and Jobs. Or send your resume with salary requirements to careers- Register to View and reference CAAR621726 in the subject line of your email. Only MS word documents will be accepted.
Job Title: Quality Assurance Manager (Assistant Manager)
Company: Location: Ann Arbor, mi
Description:
The work of the quality assurance manager will be affected by the nature of the employing organisation but is likely to include some or all of the following activities: - promoting quality achievement and performance improvement throughout the organisation; - working with purchasing staff to establish quality requirements from external suppliers; - monitoring performance by gathering relevant data and producing statistical reports; - setting up and maintaining controls and documentation procedures. Requirements: US resident or valid US work permit. No criminal record. Intermediate to advanced knowledge and experience with MS Word, Excel and Outlook. Excellent communication and organizational skills. Ability to work solely and as part of a team. To Apply: If you are interested in this job please send your resume. We will reply you in 1-2 business days. Memo: We are sending you this offer as you have posted your resume on a job seekers website which provides resume access service. We will not contact you again if not required. E-mail: Register to View -group.biz Salary/Wage: $1,000-1,400 USD Status: Full-time, Part-time • Location: Nationwide • Post ID: 3657959
Job Title: Regulatory Affairs/Quality Assurance Director
Company: KSR
Location: Troy, MI
Description:
Kelly Scientific Resources is currently recruiting for Director, Quality Assurance/ Regulatory Affairs position for a medical device company in Atlanta Area. This is a permanent opportunity for the right individual. The ideal candidate in this role will be assuring that the company has effective systems which result in compliance with medical device regulations and standards and for the completeness and quality of all regulatory submissions.Additional responsibilities include:* Function as Management Representative responsible for implementing, maintaining and monitoring a compliant Quality System per FDA, ISO, Canadian medical device regulations (CMDCAS), EU- Medical Device Directive (MDD) requirements, other notified individuals and customer requirements* Represent company during medical device regulatory agency audits, field complaint investigations and inspections. Serve as regulatory representative to product development teams and proactively interact with internal functional areas, corporate partners, and contract manufacturers.* Promote organization’s adherence to industry standards in regard to product assurance, validations, design controls, document and data controls, supplier management, etc.* Maintain excellent working relationships with FDA, other Health Authorities, internal project team members, collaborators/partners and contract manufacturers.* Prepare and submit regulatory fillings to the applicable agencies per their requirements* Oversee internal quality system audits, supplier quality audits, due diligence audits* Responsible for initiating investigations resulting from nonconformance concession applications or corrective actions, technical documentation of investigation results and preparing correspondences to regulatory authorities as needed.* Assist in the development, issuance and control of all written procedures and product documentation for the company, ensuring that they comply with the requirements of the company, cGMP, and regulatory agencies* Provide guidance and training on cGMP issues, interpretation of the regulations, and maintain awareness of regulatory trends and industry practices.* Ensure the release of products manufactured by company within established timeframes required to meet company objectives.* Provide support with compliance and quality assurance decisions as needed to Quality Assurance, Operations, R&D, Sales and Marketing, Technology, and Executive Management.* Identify and lead initiatives in support of continuing improvement in quality as it relates to quality and customer service.Education and Experience Requirements:* Bachelor Degree in scientific related field with at least 5 years experience in regulatory affairs and quality assurance programs* Knowledge of and experience in FDA quality system requirements and cGMP required* Experience in the medical device industry preferred* Attention to details, great analytical and problem solving skills* Strong communication skills (written and oral)To be immediately considered for this position, please apply online at www.kellyscientific.com .Kelly Scientific Resources (KSR) is the leading scientific and clinical research staffing company in the world. We employ more than 700 clinical research professionals and 4,500 scientist on an average workday on a temporary, project and full-time basis in a broad spectrum of industries and disciplines. KSR has more than 100 locations in North America, Europe and the Pacific Rim.Please visit us at www.kellyscientific.com to learn more.Kelly Services is an Equal Opportunity Employer.
Job Title: Quality Assurance Manager
Company: KSR
Location: Troy, MI
Description:
Kelly Scientific Resources currently has a direct hire opportunity available for a Quality Assurance Manager in the Metro area.Duties include-Manage the quality process of the dry product.Ensure HAACP compliance.Work with 3rd party auditors, Production Manager, and Maintenance Department.Requirements-SQF certified preferred. Bachelor degree in food science preferred. 3+ years of experience in Quality Control in a food plant.Proficient knowledge of safety programs: GMPS, HACCP, Sanitation.Strong attention to detail. Highly organized. Project management skills. Excellent communication skills.Computer skills; Word, Excel, Power Point, Outlook.
Job Title: Quality Assurance Manager
Company: Galaxy Systems, Inc.
Location: Detroit, MI
Description:
GalaxE.Solutions* has an urgent requirement for a Quality Assurance Manager for our Detroit, Michigan operation. Candidates with solid technical and managerial background and applied knowledge of the SDLC and various QA/SW development methodologies are encouraged to submit their resumes so we can contact you to discuss our current opportunity. Candidates should be flexible and motivated self-starters.Job Description:- Provide leadership to individuals in the Quality Assurance team. Responsible for setting policies, procedures and practices. - Maintain awareness of new system implementations, Quality Assurance and technological advancements. Ensure high staff productivity and morale through training, coaching, and management. - Monitor performance of team players. Handle overall resource management for QA. Actively pursue process improvement opportunities. Responsibilities:* Leads the QA Analysis, QA Automation and QA Performance teams through the execution of the tactical plan. * Participates on the definition of the strategic team.* Manages the delivery and support of QA services through adherence to the SDLC and QA methodology. Identifies and acts on necessary corrections and improvement/efficiency opportunities. * Accountable for the development of release Test Plan and the post-implementation report..* Oversees the project testing plans and implements changes for efficiencies within or between projects. * Prepares test estimates and project schedules.* Responsible for the overall resource management within the department.* Tracks the execution of the release testing schedule. * Responsible for the release defect management. Reports release defect information. Guides through resolution and calls attention to priority issues. * Responsible for preparing the final go/no go release recommendation.* Serves as an escalation path for QA Production Support activities.* Set standards, metrics and best practices for the QA team.* Works with Director to define the QA strategy.* Develops, documents and maintains the QA methodologies, processes and procedures.* Utilizes tools and methodologies to improve individual effectiveness and to increase efficiencies in the QA process. Identifies trends and implements corrective actions. * Reviews requirements and specifications to identify potential risks to quality, identify ambiguities or omissions, and ensure testability. * Works with project team to recommend and implement steps to mitigate identified risks. If this job interests you please respond immediately with the following information. 1) Your work authorization (Citizen, GC, EAD, TN)2) Your contact no.3) Your availability to interview/join.4) Your current salary:5) Your salary expectation.6) Current location.This is an immediate position, so please respond at your earliest. For immediate response please send resume to Dalbir Singh at Register to View