What are the responsibilities and job description for the Regulatory Affairs Specialist position at Applied Medical Technology, Inc. (AMT)?
Description
Since 1985, our core business has been enteral device product development, design, manufacturing, and engineering in a state-of-the-art facility near Cleveland, Ohio. AMT’s steady growth consistently creates job opportunities in Northeast Ohio. We are always searching for new talent and would love for you to join our team! We strive to keep the small company feeling while still reaching users all over the globe.
Position Summary
This position is responsible for revising labels, directions for use, and other documentation for submission to various regulatory agencies - most notably those pertaining to the European Medical Device Regulation. Additionally the position will help maintain and improve upon international compliance. Candidate must possess the ability to work well in a team environment and demonstrate great attention to detail.
Duties And Responsibilities
This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties may be assigned.
Requirements
Minimum Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education And/or Experience
Ability to communicate across functions, professional levels and background.
Computer Skills: Intermediate to advanced knowledge of Microsoft Office Suite.
Essential Job Functions: Critical features of this job are described below. They may be subject to change at any time due to reasonable accommodation or other reasons.
Mental: Must be able to effectively communicate with others; complete and understand complex situations, analysis of numbers; read, analyze and interpret written materials; work with team to meet and exceed company standards; ensure compliance with company policies; respond appropriately to feedback to make improvements; maintain positive working relationships; troubleshoot and solve problems.
Physical: Must be able to communicate for hours at a time, use computer equipment. Moderate noise level and limited exposure to physical risk.
Knowledge, Skills, and Abilities Required: Knowledge of modern business communication, office procedures and methods. Skill to use a personal computer and various software packages such as Microsoft Office Suite. Ability to establish priorities, work independently with minimal supervision, and facilitate teamwork.
Equipment Used: Telephones, computer, other office equipment as needed.
Special/ Additional Requirements: Persons in this position may be required to pass a drug, alcohol, and/or criminal background check.
AMT is Equal Opportunity/Affirmative Action Employer
Benefits
Since 1985, our core business has been enteral device product development, design, manufacturing, and engineering in a state-of-the-art facility near Cleveland, Ohio. AMT’s steady growth consistently creates job opportunities in Northeast Ohio. We are always searching for new talent and would love for you to join our team! We strive to keep the small company feeling while still reaching users all over the globe.
Position Summary
This position is responsible for revising labels, directions for use, and other documentation for submission to various regulatory agencies - most notably those pertaining to the European Medical Device Regulation. Additionally the position will help maintain and improve upon international compliance. Candidate must possess the ability to work well in a team environment and demonstrate great attention to detail.
Duties And Responsibilities
This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties may be assigned.
- Revise and prepare labels, directions for use, and other documentation for submission to regulatory agencies.
- Assist with biocompatibility documentation.
- Assist with the preparation and submission of regulatory filings, including European Medical Device Regulation compliant Technical Files.
- Create and/or modify regulatory documents and procedures to remain in compliance with European, ISO, FDA, ISO, Canadian, and other standards.
- Work with the international department on various regulatory filings for product registration in different countries.
- Provides regulatory support for other projects as required.
- Updating appropriate personnel on new and revised processes and procedures.
- Process, execute, organize and archive various internal documentation related to Engineering and/or Quality Systems.
- Preparing change order documentation and routing it for final approval.
Requirements
Minimum Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education And/or Experience
- Minimum of 2 year college degree, Bachelor’s Degree (or greater) preferred.
- Relevant work experience, preferably in the medical or legal field and/or other regulated industry.
- Previous experience creating and revising labels and DFUs preferred.
- Knowledge of European, ISO 13485 and FDA regulations preferred.
- Knowledge of international regulatory guidelines regarding GMP requirements is desirable.
Ability to communicate across functions, professional levels and background.
Computer Skills: Intermediate to advanced knowledge of Microsoft Office Suite.
Essential Job Functions: Critical features of this job are described below. They may be subject to change at any time due to reasonable accommodation or other reasons.
Mental: Must be able to effectively communicate with others; complete and understand complex situations, analysis of numbers; read, analyze and interpret written materials; work with team to meet and exceed company standards; ensure compliance with company policies; respond appropriately to feedback to make improvements; maintain positive working relationships; troubleshoot and solve problems.
Physical: Must be able to communicate for hours at a time, use computer equipment. Moderate noise level and limited exposure to physical risk.
Knowledge, Skills, and Abilities Required: Knowledge of modern business communication, office procedures and methods. Skill to use a personal computer and various software packages such as Microsoft Office Suite. Ability to establish priorities, work independently with minimal supervision, and facilitate teamwork.
Equipment Used: Telephones, computer, other office equipment as needed.
Special/ Additional Requirements: Persons in this position may be required to pass a drug, alcohol, and/or criminal background check.
AMT is Equal Opportunity/Affirmative Action Employer
Benefits
- Insurance: AMT offers major medical, dental, and vision insurance at the first of the month following 30 days of service.
- Other Benefits: AMT offers several other voluntary benefits including hospital indemnity, critical illness, term life insurance & long term disability (company paid), among others.
- 401k: AMT matches 100% of your contribution, up to 3% of your salary.
- Paid Time Off (PTO): In addition to nine paid holidays, AMT provides employees with paid time off (determined by length of service), starting on day one
- Family-oriented, Positive Working Environment
- Discretionary Yearly Raises
- On-site Vending & Gym
- Annual Employee Appreciation Picnic
- Tuition Reimbursement
- Employee Referral Bonus Program
- Employee Assistance Program