bioMerieux Inc.
Description
A member of the RA team is responsible for developing regulatory strategy and assessing regulatory risks for products (for both registration and change), driving IVD (as well as RUO, Veterinary, and/or Clinical Industry) products through government/regulatory approval processes. Capture and communicate worldwide regulatory requirements for product development, global product registrations, and / or life cycle management. Preparation of FDA and EU submission files and communication with Health Authorities to ensure regulatory approval. This position may require support from more senior RA members/RA managers.
Primary Duties
Organize, updating, and maintain regulatory documentation in accordance with company policy and procedures.
Participate in the preparation of regulatory submissions (US, EU, Global) and additional information or responses as requested by regulatory agencies.
Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
Perform interpretation of regulatory rules or rule changes and ensure their proper communication through corporate policies and procedures.
Perform assessment of change requests (device/labeling), with minimal oversight.
Write or update standard operating procedures and work instructions.
Begin to advise project teams on subjects such as premarket requirements, registration requirements, compliance issues, and export and labeling requirements, with some oversight from more senior regulatory specialist / manager.
May begin to mentor or train more junior regulatory personnel/trainee, where applicable.
Can be given tasks with relatively little oversight and trusted to complete them appropriately.
Can lead meetings and guide discussions regarding regulatory topics.
Can be assigned projects to lead on their own with some guidance from senior regulatory employees/managers.
Ensures accurate population of databases for tracking global product registrations.
Perform all work in compliance with company quality procedures and standards.
Performs other duties as assigned.
Qualifications Education and Training
Bachelor degree required
Science background is preferred
Experience
2+ years of regulatory affairs experience
Medical device/IVD industry preferred
Knowledge, Skills, and Abilities (KSAs)
Functional skills including critical thinking, adaptability, time management, communication, problem-solving and digital literacy
Flexibility, being highly adaptable and resilient to thrive in a dynamic work environment
Leading without authority through influence and guidance of others towards a common goal by using expertise, persuasion, and personal qualities to inspire action
Technical learning aptitude to quickly understand and acquire new technical knowledge and skills
Knowledge of MD/IVD requirements or equivalent preferred
Learning agility to be able to learn from experiences and apply that knowledge to new situations
Critical thinking, using logic and reason to analyze information and make decisions in the workplace
Detail orientation to complete tasks without errors and produce high-quality work
Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time
Effectively deal with ambiguity requiring adaptability, critical thinking, and proactive communication to navigate situations with limited details
Perspective to see the world from another person's viewpoint thus gaining new insights and finding creative solutions to challenges
Influence change using skills and relationships to persuade others to adopt new ideas, behaviors, or processes
Thriving in a fast-paced environment by managing tasks, multitasking, and adapting quickly to maintain productivity
Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently
Informing others by sharing clear, timely information to ensure alignment
Troubleshooting issues to identify and resolve problems efficiently
Driving continuous improvement by evaluating processes and implementing necessary changes
Demonstrates assertiveness and confidence in the face of a challenge
Solution oriented in the face of conflict
Ability to deal with difficult situations in a timely and bold manner
Make a stand in the presence of opposition
Action Oriented: Takes action even when facing challenges
Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives
Ability to cooperate with others at all levels including leadership
Effective Presentation Skills - including the ability to present technical data
Written Communications - including the ability to communicate technical data in written form
Effective verbal communication skills
Build and maintain positive, productive interactions with colleagues
Fosters a culture of inclusiveness among all team members
Ability to work well within a global team environment
Emotional intelligence by having the ability to recognize, understand, and manage one's own emotions, as well as the emotions of others
Consistently uphold and reflects the core ethical principles and values that bioMerieux promotes
Maintain composure by having the skill of staying calm, focused, and professional in high-pressure or stressful situations
Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMerieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at [emailprotected].
BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).
#J-18808-Ljbffr
Primary Duties
Organize, updating, and maintain regulatory documentation in accordance with company policy and procedures.
Participate in the preparation of regulatory submissions (US, EU, Global) and additional information or responses as requested by regulatory agencies.
Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
Perform interpretation of regulatory rules or rule changes and ensure their proper communication through corporate policies and procedures.
Perform assessment of change requests (device/labeling), with minimal oversight.
Write or update standard operating procedures and work instructions.
Begin to advise project teams on subjects such as premarket requirements, registration requirements, compliance issues, and export and labeling requirements, with some oversight from more senior regulatory specialist / manager.
May begin to mentor or train more junior regulatory personnel/trainee, where applicable.
Can be given tasks with relatively little oversight and trusted to complete them appropriately.
Can lead meetings and guide discussions regarding regulatory topics.
Can be assigned projects to lead on their own with some guidance from senior regulatory employees/managers.
Ensures accurate population of databases for tracking global product registrations.
Perform all work in compliance with company quality procedures and standards.
Performs other duties as assigned.
Qualifications Education and Training
Bachelor degree required
Science background is preferred
Experience
2+ years of regulatory affairs experience
Medical device/IVD industry preferred
Knowledge, Skills, and Abilities (KSAs)
Functional skills including critical thinking, adaptability, time management, communication, problem-solving and digital literacy
Flexibility, being highly adaptable and resilient to thrive in a dynamic work environment
Leading without authority through influence and guidance of others towards a common goal by using expertise, persuasion, and personal qualities to inspire action
Technical learning aptitude to quickly understand and acquire new technical knowledge and skills
Knowledge of MD/IVD requirements or equivalent preferred
Learning agility to be able to learn from experiences and apply that knowledge to new situations
Critical thinking, using logic and reason to analyze information and make decisions in the workplace
Detail orientation to complete tasks without errors and produce high-quality work
Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time
Effectively deal with ambiguity requiring adaptability, critical thinking, and proactive communication to navigate situations with limited details
Perspective to see the world from another person's viewpoint thus gaining new insights and finding creative solutions to challenges
Influence change using skills and relationships to persuade others to adopt new ideas, behaviors, or processes
Thriving in a fast-paced environment by managing tasks, multitasking, and adapting quickly to maintain productivity
Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently
Informing others by sharing clear, timely information to ensure alignment
Troubleshooting issues to identify and resolve problems efficiently
Driving continuous improvement by evaluating processes and implementing necessary changes
Demonstrates assertiveness and confidence in the face of a challenge
Solution oriented in the face of conflict
Ability to deal with difficult situations in a timely and bold manner
Make a stand in the presence of opposition
Action Oriented: Takes action even when facing challenges
Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives
Ability to cooperate with others at all levels including leadership
Effective Presentation Skills - including the ability to present technical data
Written Communications - including the ability to communicate technical data in written form
Effective verbal communication skills
Build and maintain positive, productive interactions with colleagues
Fosters a culture of inclusiveness among all team members
Ability to work well within a global team environment
Emotional intelligence by having the ability to recognize, understand, and manage one's own emotions, as well as the emotions of others
Consistently uphold and reflects the core ethical principles and values that bioMerieux promotes
Maintain composure by having the skill of staying calm, focused, and professional in high-pressure or stressful situations
Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMerieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at [emailprotected].
BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).
#J-18808-Ljbffr