Product Complaint Specialist - Irvine

Stryker is hiring a Product Complaint Specialist in Irvine. · Drive accurate and timely complaint processing that ensures device performance meets global standards. · Maintain complete and accurate complaint records in alignment with U.S. and international regulatory requirements ...

Developing and implementing a compliant quality system for products and services. · Experience in Medical Device, Life Sciences or Healthcare industry. · ...

The Director, Quality Customer Complaints · provides strategic leadership and oversight of Masimo's global complaint handling process. This role is responsible for ensuring timely, consistent and accurate processing of customer complaints; driving cross-functional investigations; ...

The Director, Quality Customer Complaints provides strategic leadership and oversight of Masimo's global complaint handling process. · This position plays a critical role in shaping complaint strategy, identifying systemic risks and trends.Provide strategic direction for the glo ...

+ The Principal Quality Engineer will play a critical role in ensuring the ongoing safety, efficacy, and compliance of our medical devices after they have entered the market. · + This senior-level role provides technical leadership and strategic oversight of post-market quality a ...

We are hiring a Senior Technical Investigation Specialist to engage and ensure appropriate product compliance in line with SOPs and RA/QA requirements. · Act as senior level investigator on all assigned tasks · Ensure quick resolution and documentation of customer inquiries. · ...

We are hiring a Senior Technical Investigation Specialist to ensure product compliance and participate in customer complaint and inquiry processes. The ideal candidate will have experience in technical support or customer service and quality assurance/regulatory affairs/complianc ...

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. · ...

Kelly Science & Clinical seeks Quality Assurance Specialist for an 8-month contract position at a premier pharma company in Irvine. · Ensure compliance with cGMP regulations and internal SOPs across all activities. · Review GMP records and release products. · ...

+We are hiring a Senior Technical Investigation Specialist. · +Act as senior level investigator on all assigned tasks · Ensure quick resolution and documentation of customer inquiries. · ...

This client is a leading CDMO providing services for the entire drug product lifecycle. · Ensure compliance with cGMP regulations and internal standard operating procedures (SOP) across all activities. · Review GMP records, including batch and laboratory documentation, and coordi ...

The Customer Care Specialist will document and communicate customer complaints in a timely manner to enhance patient care and customer satisfaction. · ...

The Customer Care Specialist will document, communicate, and follow up on customer complaints, inquiries, and product service requests in a timely and accurate manner to ensure compliance with regulations, · enhancing patient care, · and customer satisfaction.Accurately record al ...

The Customer Care Specialist will document and communicate customer complaints in a timely manner to ensure compliance with regulations enhancing patient care and customer satisfaction. · ...

Shin Imaging Center is looking for a Sales Specialist to join their team. The ideal candidate will have strong analytical and critical thinking skills, excellent customer service and leadership skills. · ...

R&D Partners is seeking to hire a Rep, Patient Registry in Irvine, CA. Your main responsibilities include sorting and organizing incoming mail by date, · preparing data records for entry in system, · collecting missing information from external customers including hospital staff ...

Due to our continued expansion and growth, we now have an opportunity for a full-time Temporary Collections Specialist at our Headquarters located in Irvine CA. · ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function and is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) experience ...

Johnson & Johnson MedTech Electrophysiology is recruiting for a Sr. Specialist, Scientific Operations to join the team in Irvine, CA or Raritan,NJ. · ...

Job summary: · This position is with Johnson & Johnson MedTech Electrophysiology. · ...