Quality Complaint Specialist, Medical Devices

**Prestigious billion dollar medical device company targeting a Complaint Specialist to join our fantastic team!** **Role is temp 6-9 months minimum** Hybrid schedule, Monday, Tuesday and Thursday onsite Irvine. Start time flex 7am-9am Comp $30-$40/hr **Must have**: - Medical Device Class III, or Dental experience - Complaint Specialist experience -...

Our Client is looking for Quality complaint Investigator Below are the details for this Job profile. Key Responsibilities: • Manage customer relationships and expectations during the course of complaint investigation and resolution process • Research, seek information and input, and challenge as appropriate, from Product Safety, Engineering and other...

Our Client is looking for Quality complaint Investigator Below are the details for this Job profile.Key Responsibilities:• Manage customer relationships and expectations during the course of complaint investigation and resolution process• Research, seek information and input, and challenge as appropriate, from Product Safety, Engineering and other...

Our Client is looking for Quality complaint Investigator Below are the details for this Job profile.Key Responsibilities:• Manage customer relationships and expectations during the course of complaint investigation and resolution process• Research, seek information and input, and challenge as appropriate, from Product Safety, Engineering and other...

Our Client is looking for Quality complaint Investigator Below are the details for this Job profile.Key Responsibilities:• Manage customer relationships and expectations during the course of complaint investigation and resolution process• Research, seek information and input, and challenge as appropriate, from Product Safety, Engineering and other...

About Beta Bionics Beta Bionics, Inc. is a medical technology company dedicated to bringing innovative type 1 diabetes management solutions to the many, not the few. We are committed to bringing better access to better solutions - and a better life for those living with diabetes - with the world's first bionic pancreas called the iLet. The iLet Bionic...

Job Description: Pay Range $35.23hr - $40.23hr Responsibilities: Investigate complex manufacturing product quality and compliance issues reported from the field, analyze results, determine root cause/probable cause, and initiate and review reports. Perform hands-on device investigation using visual, dimensional, and test equipment to...

Job DescriptionJob Summary The Manager, Quality Complaints MDR/MDV is responsible for managing the complaint handling process related to the documentation, investigation, timely processing, reporting with emphasis on Medical Device Reports (MDR) and Medical Device Vigilance (MDV). Duties & Responsibilities Manage the day to day complaint handling process...

**Essential Functions**: - Leads the daily activities of the complaints department. - Maintains QMS documentation required for complaint processing compliance with 21 CFR part 820.198 and MDSAP program. - Organizes reporting of department operations to track department status. - Files FDA Medical Device Reporting (MDR) and Health Canada incident reports. -...

Role : Quality Engineering / Compliance Specialist Location : Irvine, CA - 92614 Duration : 9 Months Skills Looking For Working on complaint evaluation for a medical device company Responsibilities include intake, investigation, and summary writing for complaints Basic computer proficiency required. Experience with quality management systems is preferred but...

The Complaints Specialist will be responsible for maintaining the quality processes associated with regulatory reporting and its procedures/controls to ensure that all MDR reportable complaints are processed and submitted in accordance with established company procedures and worldwide regulations and standards. The candidate will review reportable and...

The Complaints Specialist will be responsible for maintaining the quality processes associated with regulatory reporting and its procedures/controls to ensure that all MDR reportable complaints are processed and submitted in accordance with established company procedures and worldwide regulations and standards. The candidate will review reportable and...

Sr. Quality Engineer Irvine CA 92618 Contract (C2C)Experience - 5+ years Mandatory skills:: Quality Management, Medical Device, Regulatory Standards, Quality Compliance, CAPA / NCExperience Required:-A minimum with 5+ years of related experience Quality Management in Medical Device IndustryTechnical/Functional Skills Knowledge of Medical procedure and...

Position: Senior Regulatory Affairs Specialist Employment type: 1 year Contract/ Permanent Location: Jacksonville, FL or Irvine CA - 2 days per week ClinChoice is a global CRO that offers high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Some of these services include clinical operations, project management,...

Job Description: Pay Range: $35.23hr - $40.23hr Responsibilities: Perform customer complaints investigations, providing detailed analysis of the process and the data; determine root causes of the nonconformities in order to establish corrective and preventive actions. Execute complaint investigations multifunctional approach and issues...

Job Title: Software Quality Engineer (Medical Devices) Location: Irvine CA Duration:06 months (Possibility of extension) Summary The main function of this is to lead all software engineering activities relating to the validations of several production equipment with custom software. The main purpose of this role is to apply knowledge of software quality...

Sr. Quality Engineer Irvine CA 92618 Contract (C2C) Experience - 5+ years Mandatory skills:: Quality Management, Medical Device, Regulatory Standards, Quality Compliance, CAPA / NC Experience Required:- A minimum with 5+ years of related experience Quality Management in Medical Device Industry Technical/Functional Skills Knowledge of Medical procedure...

Sr. Quality Engineer Irvine CA 92618 Contract (C2C) Experience - 5+ years Mandatory skills:: Quality Management, Medical Device, Regulatory Standards, Quality Compliance, CAPA / NC Experience Required:- A minimum with 5+ years of related experience Quality Management in Medical Device Industry Technical/Functional Skills Knowledge of Medical procedure...

Position: Quality Engineer I (Complaint Investigations), Req#: 6086-1 Position: Quality Engineer II (Complaint Investigations), Req#: 6085-1 Both are short-term (3 months only with no possibility of extension/conversion) contract jobs. Position: Quality Engineer I/II (Complaint Investigations) Location: Irvine, CA (100% onsite) Duration: 3 Months Contract...

Position: Quality Engineer I (Complaint Investigations), Req#: 6086-1 Position: Quality Engineer II (Complaint Investigations), Req#: 6085-1 Both are short-term (3 months only with no possibility of extension/conversion) contract jobs. Position: Quality Engineer I/II (Complaint Investigations) Location: Irvine, CA (100% onsite) Duration: 3 Months Contract...