Mgr Regulatory Affairs Sr

Canon Medical Systems USA, Inc.
Tustin, California, US
Full-time

Mgr Regulatory Affairs Sr - req1224

A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible.

OVERVIEW

Manages the day to day activities of the Regulatory Affairs (RA) pre-market group. Responsible for pre-market and post-market activities as assigned by the Director, Regulatory Affairs to include new product planning and remedial actions on released products.

Participate in trade association activities to ensure that the interests of Canon Medical Systems are represented. Provide input and assist in determining the appropriate regulatory strategies for product clearance.

RESPONSIBILITIES

  • Participate in the planning of meetings between the FDA and CMSU regarding regulatory issues as assigned by the Director, Regulatory Affairs.
  • Provide leadership to include supervision and mentoring of pre-market RA staff.
  • Provide guidance to CMSC Business Unit Managers and Engineering Managers in FDA Approval preparation.
  • Support activities related to FDA compliance activities including GMP inspections, recalls and MDR's as assigned by the Director, Regulatory Affairs.
  • Support legal actions as required by the legal department or directed by the Director, Regulatory Affairs.
  • Provide training to CMSU and CMSC employees on regulatory items.
  • Regularly audit CMSU's policies and procedures.
  • Track pending FDA submissions (510's, PMA's), IDE, and IRB.
  • Serve in lieu of the Director Regulatory Affairs as required.

QUALIFICATIONS

  • Current knowledge of all laws pertaining to FDA clearance.
  • 10 years Direct FDA experience and management experience.
  • 4 Year / Bachelor's Degree in Regulatory, Engineering or Physical Sciences.

About us!

Canon Medical Systems USA, Inc., a world leader in diagnostic imaging, is in search of qualified candidates to fill our open positions.

Canon Medical Systems offers a competitive salary and benefits package, we support a diverse workplace and are an equal opportunity employer.

All qualified applicants will receive consideration for employment without regard to race, sex, color, sexual orientation, gender identity, religion, national origin, protected veteran status, or on the basis of disability.

We invite you to join and become part of our Canon family.

J-18808-Ljbffr

2 days ago
Related jobs
Promoted
Canon Medical Systems USA, Inc.
Tustin, California

Mgr Regulatory Affairs Sr - req1224. Participate in the planning of meetings between the FDA and CMSU regarding regulatory issues as assigned by the Director, Regulatory Affairs. Manages the day to day activities of the Regulatory Affairs (RA) pre-market group. Responsible for pre-market and post-ma...

Promoted
University of California - Irvine
Orange, California

Under the supervision of the Regulatory Program Manager (RPM) of the Regulatory Affairs Unit, the Senior Regulatory Affairs Coordinator (SRAC) supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing study start-up regulatory management for high-priority can...

Promoted
Acara Solutions, An Aleron Company
Brea, California

Regulatory Affairs Specialist creates, evaluates, and completes regulatory tasks related to the following: worldwide product registration submissions, facility registrations, technical files, FDA submissions, special projects, and strategy to drive market growth worldwide. Creates and implements reg...

Promoted
STAAR Surgical
Lake Forest, California

Support for regulatory publishing including assembling, printing, quality checking, archiving of regulatory submissions and corresponding data. Plan, prepare and review all aspects of ongoing and new regulatory submissions, both U. Compile information necessary for periodic reports for Regulatory fi...

Promoted
STAAR Surgical
Lake Forest, California

Support for regulatory publishing including assembling, printing, quality checking, archiving of regulatory submissions and corresponding data. Plan, prepare and review all aspects of ongoing and new regulatory submissions, both U. Compile information necessary for periodic reports for Regulatory fi...

Promoted
STAAR Surgical
Lake Forest, California

Support for regulatory publishing including assembling, printing, quality checking, archiving of regulatory submissions and corresponding data. Plan, prepare and review all aspects of ongoing and new regulatory submissions, both U. Compile information necessary for periodic reports for Regulatory fi...

MicroVention
Aliso Viejo, California

As a contributing member on product development and operation teams, at times act as sole representative from Regulatory to ensure regulatory compliance. Prepare and file regulatory submissions to ensure MicroVention devices are commercially available in the assigned market(s) based on the approved ...

Entegee
Irvine, California

Seeking a Senior Regulatory Affairs Specialist with expertise in US and EU regulatory requirements, EU MDR regulation, and medical device regulatory submissions to sustain the current product portfolio. Partner with the international regulatory affairs group to support regulatory submissions. In-dep...

Glidewell
Irvine, California

Minimum five (5) years of experience in Regulatory Affairs. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Prepare and submit product registrations and submissi...

Acara Solutions
Brea, California

Maintains current knowledge of relevant regulations, including proposed and final rules issued by relevant regulatory authorities that may impact the company-Creates and implements regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced-Technical wri...