Job Description DESCRIPTION : Artech is currently seeking to add to the below position Job Title: Systems Programmer z/OSJob ID: 21-16268Location: Remote/Work from home Duration: 12 Months+ contractJob Description:Experienced z/OS Systems Programmer whose responsibilities include upgrading and apply...
Job Description DESCRIPTION : Artech is currently seeking to add to the below position Job Title: z/OS Systems Programmer Job ID: 21-47798Location: Remote/Work from home Duration: 12 Months+ contractJD Experienced z/OS Systems Programmer whose responsibilities include upgrading and applying maintena...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
What you will be a part of:As a Mainframe Engineer you will help build, support, and maintain our zOS Mainframe agents. This engineer will help design, develop and drive continuous integration on our product and Mainframe suite.Qualifications/RequirementsExperience with IMS DC, Assembler and z/OSExp...
TCI has an immediate need for a Remote Senior Mainframe Systems Engineer at Fort Knox, KY. This is not a Corp2Corp opportunity. This is a long-term contract opportunity with probable extensions and possible hire. In addition to competitive, market-rate based pay, TCI provides all our Consultants wit...
Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11)Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical educa...
Requisition ID: 48259 Title: Senior Specialist, Regulatory Affairs - Medical Device Imaging Systems and SaMD Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11) Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical...
Regulatory Affairs Specialist Seeking a Regulatory Affairs Specialist who will be responsible for the preparation of regulatory submissions required to market or investigate new or modified medical devices in both domestic and international markets. This responsibility entails supporting the develop...
Position Description:Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing regulatory strategies, preparing U.S. and international submissions and obtaining and maintaining approval for products and therapies to markets worldw...
A bit about us:Our client is a growing medical device company with an exciting product for skin repairWhy join us?Stock Options401k with a Generous MatchMultiple Health Care PlansDental/VisionCompany-sponsored Short-Term Disability, Long-Term Disability and Life InsuranceJob DetailsPrimary FunctionT...
Regulatory Affairs Specialist Seeking a Regulatory Affairs Specialist who will be responsible for the preparation of regulatory submissions required to market or investigate new or modified medical devices in both domestic and international markets. This responsibility entails supporting the develop...
Job Description: Pay Range $45hr - $50hr At least 5+ years of experience as a core system programmer in Umbrella preferably supporting IDS product. Strong Experience in Assembler language programming. Should be able to work with VSAM databases in Hogan. Experience leading and working through an umbr...
Job Description: Pay Range $45hr - $50hr At least 5+ years of experience as a core system programmer in Umbrella preferably supporting IDS product. Strong Experience in Assembler language programming. Should be able to work with VSAM databases in Hogan. Experience leading and working through an umbr...
Our client, a world leader in Life Sciences who is looking for Regulatory Affairs Specialist II(100% Remote).Job Title: Regulatory Affairs Specialist II (100% Remote)Job Type: Long-Term ContractLocation: Santa Clara, CA Responsibilities:• Manages regulatory responsibilities associated with the devel...
Requisition ID: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11) Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. ...
Requisition ID: 48218 Title: Specialist II, Regulatory Affairs - Medical Devices Division: Arthrex, Inc. (US01) Location: Inc- Work From Home (US11)Position Summary: Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex...
Remote Sr. Regulatory Affairs Specialist Duration: Contract to hire Education & Qualifications:B.S. in a technical discipline preferred or equivalent experience.4+ years experience in Regulatory Affairs in the medical device industryExpertise in working within Medical Device Regulations including Qu...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
Remote Sr. Regulatory Affairs SpecialistDuration: Contract to hire Education & Qualifications:B.S. in a technical discipline preferred or equivalent experience.4+ years experience in Regulatory Affairs in the medical device industryExpertise in working within Medical Device Regulations including Qua...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
A Remote Regulatory Affairs Specialist role in Cincinnati, Ohio is now available through Adecco Medical and Science. In this role, you will assume the responsibility for regulatory compliance of a portfolio of medical devices used with the organization's contrast media. The Regulatory Affairs person...
This Jobot Job is hosted by: Hunter PraterAre you a fit? Easy Apply now by clicking the "Apply on company site" button and sending us your resume.A bit about us:Our client is a growing medical device company with an exciting product for skin repairWhy join us?Stock Options401k with a Generous MatchM...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
This Jobot Job is hosted by: Hunter PraterAre you a fit? Easy Apply now by clicking the "Apply on company site" button and sending us your resume.A bit about us:Our client is a growing medical device company with an exciting product for skin repairWhy join us?Stock Options401k with a Generous MatchM...
At Terumo Cardiovascular, we develop, manufacture and distribute medical devices for cardiac and vascular surgery with an emphasis on cardiopulmonary bypass, intra-operative monitoring and vascular grafting. This includes a full-line of perfusion products, endoscopic vessel harvesting products and s...
At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. With over 260,000 diverse, talented and dedicated employees across 100 locations in 30 countries, our vision is to be the most technologically advanced and trusted manufacturing solutions provider. We combine an unmatched breadth an...
RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and quality consulting solutions. We exist to prom...
Job Description SummaryJob DescriptionBe part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtu...
We re hiring technical project lead with a strong science or engineering background who believes in the power of teamwork to improve the lives of patients and caregivers. Could it be you?CMD MedTech is a consulting firm in Columbus, Ohio with a focus on getting innovative medical devices to market a...
Ventura Solutions is a rapidly growing medical device and pharmaceutical niche consulting and staffing firm.Are you looking for a remote recruiter position that involves finding the very best talent for some amazing companies? Are you also looking for a new opportunity to grow with an expanding comp...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All m...
Were hiring technical project lead with a strong science or engineering background who believes in the power of teamwork to improve the lives of patients and caregivers. Could it be you? CMD MedTech is a consulting firm in Columbus, Ohio with a focus on getting innovative medical devices to market a...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All...
Great opportunity for REMOTE based Regulatory Affairs Specialist working with Medical Device! We are looking for RA Specialist to join our team in working with various Medical Device companies in REMOTE based work. Must have experience in Authoring 510k Submissions and well as FDA Submissions. All...