Quality Assurance Jobs in Mahwah, New Jersey

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46 Mahwah, NJ Quality Assurance jobs found on Monster.

Jobs 1 to 20 of 46
Compliance Specialist Bergen County NJ Essential Job Function: Responsible for interacting with customers on quality issues. Responsible for the receipt of all Notices of Investigations and logging them into the Investigations spreadsheet. Responsible for the receipt of independent CAPAs and logging them into the CAPA spreadsheet. Responsible for reviewing investigation reports for accuracy, compl...
Job Summary: Supports activities of the Quality Assurance Department in regards to third party manufacturers/packagers to ensure that Par remains in compliance with all relevant pharmaceutical regulatory requirements i.e. FDA GMP. Developsand/or supports objectives, strategies, systems and procedures for QA oversight of third party manufacturers with supervision of direct Management. Interfaces wi...
Test Planning, Test Strategy, Mainframe Testing, Test Data Creation, Test Automation, Web testing (Preferable) REQUIREMENTS Education Experience 3 - > 25 years...
Looking for a QA Lead for one of our projects in Woodcliff Lake, NJ. Title : QA Lead Location: Woodcliff Lake, NJ Duration: Full Time Employee Interview Process: One to two phone screens followed by an in-person Responsibilities · Develop testing strategies and standards for the department · Ensure appropriate reviews for all test plans and test cases · Provide appropriate status to Project/Progra...
Full Time ISO 9001:2008 Quality Coordinator position is immediately available within our mature (5 year registered) quality system. This position requires an energetic and enthusiastic team member that will maintain the ISO system documentation as well as perform internal audits. Position requires some creation of new supporting documentation, forms, policies and plans. The position interfaces dai...
QUALITY ASSURANCE MANAGER A leading food manufacturer located in northern New Jersey has an outstanding opportunity for a Quality Assurance Manager. The successful candidate will provide leadership and play a key role in quality systems planning, research & development and sanitation. Specific Responsibilities: o Evaluating and improving the production system by implementing standards for product...
Job Description Posting date: May 2, 2014 Position Summary: Perform Quality control analysis on raw materials (dry chemicals, solvents and solutions, stains and indicators) including but not limited to the scope of in process clearance, semi finished and finished goods clearance, evaluation and method validation for compendia and regulated products for the company’s LCR source products (Low Cost R...
Job Description Posting date: May 2, 2014 Position Summary: Responsible for preparing product traceability matrices for all product lines under Med Device, Single and Multi Compendia, GMP, ACS and other critically identified regulated as well as non regulated Thermo Fisher Scientific – Global Chemical products. Supports validation activities in a cGMP regulated manufacturing, repacking and relabel...
Job Description Posting date: May 6, 2014 Position Summary: Lead and perform regulatory and compliance activities for the company’s regulated products (Multi compendia Production chemicals, cGMP products and medical device products) as directed with primary responsibility for USFDA and Secondary responsibilities for MHRA, TGA, SFDA. Provide International (outside North America) regulatory submissi...
Job Description Posting date: May 15, 2014 Position Summary: This position is responsible for managing the CMC (Chemical Product Manufacturing and Controls) compliance of Thermo Fisher Scientific – Global Chemicals products that include hazardous goods, laboratory and analytical reagents, Multi Compendia products, Production chemicals, Class 1 devices, and stains and indicators. Chemical classific...
Description Provides front end and departmental asset protection support to reduce incidents of fraud, theft and shrink exposure. Responsibilities: · Respond to all incident of EAS alarm activation; verification of purchase receipts against merchandise when EAS is activated; ensure merchandise is deactivated for guests; educate cashiers on proper deactivation procedures. · Provide guest service to...
Description Provides front end and departmental asset protection support to reduce incidents of fraud, theft and shrink exposure. Responsibilities: · Respond to all incident of EAS alarm activation; verification of purchase receipts against merchandise when EAS is activated; ensure merchandise is deactivated for guests; educate cashiers on proper deactivation procedures. · Provide guest service to...
Posting date: July 10, 2014 Position Summary: Lead and perform regulatory and compliance activities for the company’s regulated products (Multi compendia Production chemicals, cGMP products and medical device products) as directed with primary responsibility for USFDA and Secondary responsibilities for MHRA, TGA, SFDA. Provide International (outside North America) regulatory submission support. Co...
Posting date: May 2, 2014 Position Summary: Perform Quality control analysis on raw materials (dry chemicals, solvents and solutions, stains and indicators) including but not limited to the scope of in process clearance, semi finished and finished goods clearance, evaluation and method validation for compendia and regulated products for the company’s LCR source products (Low Cost Region). Analytic...
RESPONSIBILITIES: Our client is seeking a Sr. QA Tester for their Wayne, NJ location. This is a great opportunity but a temporary position with this company. Details of Position: Identifies problems, generates alternatives, and recommends solutions within defined processes Collaborates effectively with QA team members, application developers, software vendors, consultants, user communities, and te...
Job Description : Contract position for a QA Complaint Analyst for medical devices This position will provide support and assistance in the evaluation of Product Complaints on Medical Devices, including submission of Medical Device Reports (MDR) and Medical Device Vigilance (MDV) and reportability requirements for various countries. Investigation and documentation of field clinical events and foll...
Description Provides front end and departmental asset protection support to reduce incidents of fraud, theft and shrink exposure. Responsibilities: · Respond to all incident of EAS alarm activation; verification of purchase receipts against merchandise when EAS is activated; ensure merchandise is deactivated for guests; educate cashiers on proper deactivation procedures. · Provide guest service to...
About the Job RAB Lighting is seeking a Quality Engineer This is an exciting opportunity with a well-established, rapidly growing company on the Bergen/Rockland county border. Responsibilities • Hands-on implementation of quality systems • Support and train Customer Service reps regarding product questions and technical issues • Analyze product malfunctions and produce quantitative, written report...
Quality Technician – 2nd Shift Summary Responsible for examining materials for quality and defects, analyzing and reporting failure modes, and training RAB personnel in identification of potential quality issues and good manufacturing Practices (GMP) . Primary responsibilities Ensure quality of manufactured goods. Train personnel (Quality and Production) in identification of potential quality issu...
My client is busy and looking to add to staff an experienced Quality Manager/ Supervisor from a CNC Manufacturing work environment. Position: Quality Inspection Manager / Permanent position / 1st shift Required skills: 3-5 years of hands-on inspection supervision experience in a CNC Manufacturing environment. Solid understanding of geometric dimension and tolerance (true positions, profile toleran...
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