Quality Assurance & Safety category and Medical Devices and Supplies industry jobs

THERAKOS® is a global leader in advancing the science of extracorporeal photopheresis (ECP). For 25 years, THERAKOS® employees have pioneered new and industry leading technologies. As we look to drive the next phase of Therakos’ growth, we are seeking to expand our team with talented leaders and professionals in all functional areas. THERAKOS® offers a range of opportunities to work and grow in an...
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We have been engaged by our client to recruit their Regulatory Affairs Manager. Our client is a worldwide medical device manufacturer. This manager plays a key role for combination products representing Regulatory Affairs within the company and with global regulatory agencies. The role develops and executes strategies for global regulatory approvals to introduce new and modified medical device/dru...
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Aesculap is currently seeking a Director, Quality Operations. The primary responsibilities of this role will be to lead and monitor Quality Assurance activities for Aesculap, Inc. and Aesculap Implant Systems. This position will serve as the Management representative for both AIC and AIS Quality Systems as required by the FDA Quality System Regulation and ISO 13485 Standard. This person will be a ...
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Purpose: Provide quality engineering leadership by inspiring individuals and teams while creating an environment of organizational excellence to deliver results. Duties and Responsibilities (Key Deliverables): 1. Overall responsibility for managing Quality Engineering, Specialist support, managing key projects, and QA related aspects of the Supplier Quality Program. Apply appropriate resources and...
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MANAGER, QUALITY CONTROL INSPECTION (Medical) Purpose: The position will head the inspection group for incoming, final inspection and acceptance of critical medical devices in their Orange County Facility. It will also support the continuous improvement of the related processes and the inspection procedures. The responsibility also includes the collection and analysis of data on quality cost, scra...
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Custom Division Overview KIK's Custom Division is the #1 contract manufacturer for the Consumer Packaged Goods industry (CPG) and the largest contract manufacturer for some of the world's largest CPG companies. From shampoos, soaps, body lotions, and sunscreens, and fragrances to medical and pharma, we manufacture products found in households across North America. Our extensive portfolio of liquid...
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Ivy Sports Medicine, LLC was formed in February of 2011 to create a global healthcare company focused on providing the best sports medicine therapies for orthopedic surgeons and patients. In June 2011, ISM acquired assets from ReGen Biologics out of Chapter 11. Our Mission To build a global company that creates value for our employees, shareholders and stakeholders by collaborating with practition...
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THE CHALLENGE: A leading edge medical device manufacturer located in a desirable Arizona metro location has an immediate need for a talented Sr. Quality Engineer. The selected individual will be an key contributor to the organization and will be provided a unique and supportive corporate culture. * Key member of Product Development team—providing Design Control criteria. * Provides technical suppo...
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SENIOR QUALITY ENGINEER Medical Device Manufacturing An opportunity exists for a Senior Quality Engineer with experience in medical device project management, process improvement, and new product development in the Encinitas, CA area. The right candidate will have 8+ years in quality assurance with at least 5 of those years in medical device design and/or operations. An extensive knowledge of NPD,...
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Senior Quality Control Manager The Senior Quality Control Manager, a hands-on problem solver will manage the quality control function in the Waltham, MA facility to drive quality improvements and continuous improvement efforts associated with the quality of products and the processes and testing of analyzers and reagents. Additional responsibilities include: drive the current quality control pract...
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SUMMARY Sr. Quality Engineer shall provide technical, quantitative, and coordination support to assure products and processes are designed, deployed, and operated according to requirements. Requirements include good manufacturing practices under USFDA 21CFR820, ISO 13485, MDD, Health Canada and corporate standards. Specific Duties: ·As part of the design team, provide input to the quality attribut...
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Quality Systems Engineer – Quality Documents Medical Devices A medical device company in the Cincinnati, Ohio area has an urgent need for someone with Quality Assurance Document Control experience. The position requires 5+ years in the medical device industry and prior success managing SOPs and strong knowledge of GDPs. Insuring process documentation is accurate and consistent as well as ensuring ...
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