Collabera
Regulatory Affairs Project Leader
Collabera, Santa Clara, California, us, 95053
Description
HomeSearch JobsJob Description
Regulatory Affairs Project Leader
Contract: Santa Clara, California, US
Salary: $55.00 Per Hour
Job Code: 347954
End Date: 2024-10-03Days Left: 15 days, 3 hours left
Apply
To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you!
Pay Range - $50 to $55/hr. (negotiable)
Job Description:Job Roles & Responsibilities:Education: Bachelor's degree required, Master's degree preferredExperience: Minimum of 3 years of Regulatory Affairs experienceSkills: Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or device submissions.Hands-on experience with 510k submission, or PMA/s or US Annual report or CE Technical Documentation preparation.Assists in definition/implementation of regulatory strategy and priorities in conjunction with management, peers, commercial, and affiliate personnel.Communicates issues to management through project management tracking and issue briefings.Position is highly visible to internal and external stakeholders.High level of effective verbal and written communication skills must be demonstrated, including ability to negotiate, influence, and manage conflict. Prior regulatory experience in the medical device, food, dietary supplement, or pharmaceutical industry is strongly preferred, but not required.Ability to work constructively, decisively, and collegiality with internal customers (scientists, marketing, quality assurance, product development, affiliates) to solve problems and communicate regulatory needs.Ability to manage and track broad and strategic projects.Ability to communicate effectively in writing crisp briefings and issue analysis.Demonstrated ability to work effectively in a team environment.Responsible for tracking and timely completion of regulatory strategies and issues, scientific substantiation for product claims, and label material activities.Responsible for effective communication of regulatory requirements to project teams and internal customers.Additional Notes:
Must have RA submission experience. and EU & MU submissions experiencegood writing and communication skills - Word, ExcelBachelor's degree in engineering or science and a minimum of 3 years of experience of regulatory affairsDay to day:
Registrations - will train to do this up to 200 pages of documentation formattingComplete technical documents for different Countries and submit to government agencies as well as the US.Job Requirement
Regulatory Affairs Project LeaderRegulatory Affairs510k submission510kPMATechnical Documentationproject managementMDREU MDRMedical DeviceReach Out to a RecruiterRecruiterEmailPhoneChitrank Rastogichitrank.rastogi@collabera.com4255231648
Apply Now
HomeSearch JobsJob Description
Regulatory Affairs Project Leader
Contract: Santa Clara, California, US
Salary: $55.00 Per Hour
Job Code: 347954
End Date: 2024-10-03Days Left: 15 days, 3 hours left
Apply
To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you!
Pay Range - $50 to $55/hr. (negotiable)
Job Description:Job Roles & Responsibilities:Education: Bachelor's degree required, Master's degree preferredExperience: Minimum of 3 years of Regulatory Affairs experienceSkills: Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or device submissions.Hands-on experience with 510k submission, or PMA/s or US Annual report or CE Technical Documentation preparation.Assists in definition/implementation of regulatory strategy and priorities in conjunction with management, peers, commercial, and affiliate personnel.Communicates issues to management through project management tracking and issue briefings.Position is highly visible to internal and external stakeholders.High level of effective verbal and written communication skills must be demonstrated, including ability to negotiate, influence, and manage conflict. Prior regulatory experience in the medical device, food, dietary supplement, or pharmaceutical industry is strongly preferred, but not required.Ability to work constructively, decisively, and collegiality with internal customers (scientists, marketing, quality assurance, product development, affiliates) to solve problems and communicate regulatory needs.Ability to manage and track broad and strategic projects.Ability to communicate effectively in writing crisp briefings and issue analysis.Demonstrated ability to work effectively in a team environment.Responsible for tracking and timely completion of regulatory strategies and issues, scientific substantiation for product claims, and label material activities.Responsible for effective communication of regulatory requirements to project teams and internal customers.Additional Notes:
Must have RA submission experience. and EU & MU submissions experiencegood writing and communication skills - Word, ExcelBachelor's degree in engineering or science and a minimum of 3 years of experience of regulatory affairsDay to day:
Registrations - will train to do this up to 200 pages of documentation formattingComplete technical documents for different Countries and submit to government agencies as well as the US.Job Requirement
Regulatory Affairs Project LeaderRegulatory Affairs510k submission510kPMATechnical Documentationproject managementMDREU MDRMedical DeviceReach Out to a RecruiterRecruiterEmailPhoneChitrank Rastogichitrank.rastogi@collabera.com4255231648
Apply Now