Regulatory Affairs Intern
Position :
Regulatory Affairs Intern Location :
Covington, GA Duration :
03 Months Contract Total Hours/week :
40.
00 1st Shift
Job Description:
The position is a temporary Regulatory Affairs Internship.
College student pursuing undergrad or grad degree is appropriate for this role.
Regulatory Affairs Intern is responsible for contributing to the planning, coordinating and implementing regulatory strategies for products that require government approval.
Demonstrates working knowledge of healthcare-related regulations.
Demonstrates in-depth knowledge of preparing a submission.
Demonstrates in-depth knowledge of industry and competitive products.
Applies relevant regulations and statutes to further product submissions of basic to medium complexity.
Contributes to the strategic direction of regulatory pathway development.
Refines and conforms the preliminary data used in the submission process.
Translates technical data and descriptions into reviewer-friendly content.
Helps to ensure that the appropriate regulatory requirements for the submission are met.
Interacts with regulatory body to help further product approvals or clearance.
Has in-depth experience, knowledge and skills in own job family Applies knowledge and skills to a wide range of standard and non-standard situations Works independently with minimal guidance Usually determines own work priorities Acts as a resource for colleagues with less experience.
Recommended Skills Friendliness Health Care Regulatory Requirements Coordinating Technical Data Management Systems Strategic Thinking Estimated Salary: $20 to $28 per hour based on qualifications.
Regulatory Affairs Intern Location :
Covington, GA Duration :
03 Months Contract Total Hours/week :
40.
00 1st Shift
Job Description:
The position is a temporary Regulatory Affairs Internship.
College student pursuing undergrad or grad degree is appropriate for this role.
Regulatory Affairs Intern is responsible for contributing to the planning, coordinating and implementing regulatory strategies for products that require government approval.
Demonstrates working knowledge of healthcare-related regulations.
Demonstrates in-depth knowledge of preparing a submission.
Demonstrates in-depth knowledge of industry and competitive products.
Applies relevant regulations and statutes to further product submissions of basic to medium complexity.
Contributes to the strategic direction of regulatory pathway development.
Refines and conforms the preliminary data used in the submission process.
Translates technical data and descriptions into reviewer-friendly content.
Helps to ensure that the appropriate regulatory requirements for the submission are met.
Interacts with regulatory body to help further product approvals or clearance.
Has in-depth experience, knowledge and skills in own job family Applies knowledge and skills to a wide range of standard and non-standard situations Works independently with minimal guidance Usually determines own work priorities Acts as a resource for colleagues with less experience.
Recommended Skills Friendliness Health Care Regulatory Requirements Coordinating Technical Data Management Systems Strategic Thinking Estimated Salary: $20 to $28 per hour based on qualifications.
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