Regulatory Affairs Manager at Danaher Corporation
Sacramento, CA 94203
About the Job
Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward
Join a team where you can be heard, be supported, and always be yourself
We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates
Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher
Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The Regulatory Affairs Manager for Beckman Coulter Diagnostics is responsible for the development and execution of global regulatory strategy and tactical planning for assigned microbiology on market products or those products in development
Assures that defined regulatory strategies defined are effectively implemented and maintained in line with changing regulatory and business needs
This individual identifies and gathers data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured, or distributed to meet relevant global regulatory requirements.This position is part of the Regulatory Affairs group located in Sacramento, California and will be onsite
At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.You will be a part of the QRC team and report to the Sr
Director QRC responsible for microbiology quality, regulatory, and clinical
If you thrive in an amazing, multifunctional, leadership, fast paced, supporting role and want to work to build a world-class Regulatory Affairs organization—read on.Responsibilities:Responsible for a product(s) with multiple driver indications within a Therapeutic Area and supports the Sr
Manager Clinical Affairs in the development & execution of the regulatory strategy
Assigned matters may have a moderate impact on business activities and operations.Serves as regulatory affairs liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation and completion of FDA meeting briefing packages and responses
Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial.Key contributor responsible for the preparation and review of regulatory submissions consistent within global regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review.Recommends and implements changes to difficult projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidance, as well as corporate policies and management-related considerations.Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP).In this role, you will have the opportunity to:Lead a team of regulatory professionalsMake an impact in the antimicrobial susceptibility marketThe essential requirements of the job include:Required Education: Bachelor’s degree (pharmacy, biology, chemistry, microbiology) or industry-related with 9+ years of experience or, Master’s degree with 7+ years of experience, or PHD with 5+ years of experienceDemonstrates excellent negotiation skills, problem-solving skills and builds consensus.Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization.Able to deliver challenging messages effectively without compromising important business relationships.Proven skill at implementing successful global regulatory strategies regulatory strategies
Experience working in a complex matrix environment.It would be a plus if you also possess previous experience in:Preferred Experience: 2-3 years in diagnostics regulatory activitiesPreferred Education: Advanced Degree a plus
Certifications a plus.Software experience is a plus (e.g
Experience interfacing with government regulatory agencies surrounding cybersecurity/software development).The salary range OR the hourly range for this role is 140k to 160 k
This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting
We may ultimately pay more or less than the posted range
This range may be modified in the future.This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable
The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology
We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life
Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond
For more information, visit .Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law
We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve
Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment
Please contact us at
Join a team where you can be heard, be supported, and always be yourself
We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates
Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher
Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The Regulatory Affairs Manager for Beckman Coulter Diagnostics is responsible for the development and execution of global regulatory strategy and tactical planning for assigned microbiology on market products or those products in development
Assures that defined regulatory strategies defined are effectively implemented and maintained in line with changing regulatory and business needs
This individual identifies and gathers data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured, or distributed to meet relevant global regulatory requirements.This position is part of the Regulatory Affairs group located in Sacramento, California and will be onsite
At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.You will be a part of the QRC team and report to the Sr
Director QRC responsible for microbiology quality, regulatory, and clinical
If you thrive in an amazing, multifunctional, leadership, fast paced, supporting role and want to work to build a world-class Regulatory Affairs organization—read on.Responsibilities:Responsible for a product(s) with multiple driver indications within a Therapeutic Area and supports the Sr
Manager Clinical Affairs in the development & execution of the regulatory strategy
Assigned matters may have a moderate impact on business activities and operations.Serves as regulatory affairs liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation and completion of FDA meeting briefing packages and responses
Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial.Key contributor responsible for the preparation and review of regulatory submissions consistent within global regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review.Recommends and implements changes to difficult projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidance, as well as corporate policies and management-related considerations.Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP).In this role, you will have the opportunity to:Lead a team of regulatory professionalsMake an impact in the antimicrobial susceptibility marketThe essential requirements of the job include:Required Education: Bachelor’s degree (pharmacy, biology, chemistry, microbiology) or industry-related with 9+ years of experience or, Master’s degree with 7+ years of experience, or PHD with 5+ years of experienceDemonstrates excellent negotiation skills, problem-solving skills and builds consensus.Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization.Able to deliver challenging messages effectively without compromising important business relationships.Proven skill at implementing successful global regulatory strategies regulatory strategies
Experience working in a complex matrix environment.It would be a plus if you also possess previous experience in:Preferred Experience: 2-3 years in diagnostics regulatory activitiesPreferred Education: Advanced Degree a plus
Certifications a plus.Software experience is a plus (e.g
Experience interfacing with government regulatory agencies surrounding cybersecurity/software development).The salary range OR the hourly range for this role is 140k to 160 k
This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting
We may ultimately pay more or less than the posted range
This range may be modified in the future.This job is also eligible for bonus/incentive pay.We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable
The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology
We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life
Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond
For more information, visit .Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law
We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve
Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment
Please contact us at
applyassistance@danaher.com
to request accommodation.Job SummaryJob number: R1270898Date posted : 2024-07-15Profession: Quality & Regulatory AffairsEmployment type: Full time 