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- Tasks: Support regulatory compliance for medical devices and coordinate activities to meet standards.
- Company: Philips is a global health technology leader focused on improving lives through innovation.
- Benefits: Enjoy generous PTO, 401k matching, education reimbursement, and more perks.
- Why this job: Join a mission-driven team dedicated to making healthcare accessible for everyone.
- Qualifications: Bachelor’s degree in relevant fields; experience in regulatory affairs preferred.
- Other info: This is an office-based role requiring in-person collaboration at least 3 days a week.
The predicted salary is between 42000 - 68000 £ per year.
Regulatory Affairs Business Specialist page is loaded
Regulatory Affairs Business Specialist
Apply locations Colorado Springs San Diego Plymouth time type Full time posted on Posted 2 Days Ago job requisition id 560118
Job Title
Regulatory Affairs Business Specialist
Job Description
Regulatory Affairs Business Specialist
In this role, you will support regulatory compliance and business objectives for our Image-Guided Therapy Devices business by coordinating regulatory activities and ensuring products meet relevant medical device standards and requirements.
Your role:
- Assists in implementing comprehensive regulatory strategies by collaborating with regulatory and cross-functional teams to ensure alignment with company objectives and compliance with relevant regulations for limited scope typically smaller and less complex projects.
- Demonstrates basic understanding of Regulatory\’s role in the Quality System with basic awareness of product lines, disease states, and customers, possessing general knowledge of business developed through education or past experience.
- Collaborates with central and regional Regulatory Affairs teams to support establishment registration and listing, and UDI/Global Trade Identification Number (GTIN) related activities, maintaining processes for regulatory filings/ licenses and developing technical contribution.
- Assists in coordinating and developing conformity assessment strategies and plans essential for supporting regulatory submissions, ensuring alignment with regulatory requirements and standards.
- Supports the coordination and preparation of regulatory submissions for product/solution licensing, ensuring accuracy and completeness to expedite approval processes efficiently, managing files for device updates and related change control processes, supporting the Marketing Teams on Tender related issues.
- Participates in reviewing product/solution labeling and related marketing communications to ensure compliance with regulatory guidelines and standards, primarily at the Business and Field levels.
- Keeps abreast of regulatory procedures and changes, participates in process improvement activities related to internal regulatory processes, as well as evolving Regulatory Agency changes.
You\’re the right fit if:
- Experience in regulatory affairs, quality compliance, product development or equivalent in the medical device industry strongly preferred.
- Your skills include knowledge and experience working relevant medical device regulations and standards. Experience with Rimsys, SAP, and/or Windchill preferred.
- You have a bachelor’s degree or higher in Biomedical Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent required. RAPS RAC certification preferred but not required.
- You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position .
- You’re an excellent communicator (written and verbal) with an ability to manage and prioritize multiple deliverables based on urgency.
How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
This is an office-based role.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won\’t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
- Learn more about our business .
- Discover our rich and exciting history.
- Learn more about our purpose.
- Learn more about our culture.
Philips Transparency Details
The pay range for this position in Colorado Springs, CO is $60,750 to $97,200.
The pay range for this position in Plymouth, MN is $63,788 to $102,060.
The pay range for this position in San Diego, CA is $68,040 to $108,864.
The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here .
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.
Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Colorado Springs, CO, Plymouth, MN, or San Diego, CA.
This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.
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Director, Regulatory Affairs
locations Plymouth time type Full time posted on Posted 3 Days Ago
At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.
For more than 130 years, we have been creating technologies and innovations that improve people\’s lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.
Together, we deliver better care for more people because we believe that every human matters. That\’s why we\’re taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other\’s views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success.
It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism.
To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans\’ Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.
Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.
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Regulatory Affairs Business Specialist employer: Philips International
Contact Detail:
Philips International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Business Specialist
✨Tip Number 1
Familiarise yourself with the latest medical device regulations and standards. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in regulatory affairs, especially those who work in the medical device industry. Attend relevant conferences or webinars to make connections that could lead to job opportunities.
✨Tip Number 3
Gain hands-on experience with tools like Rimsys, SAP, or Windchill if you haven't already. Familiarity with these systems can set you apart from other candidates and show your readiness for the role.
✨Tip Number 4
Prepare for potential interviews by practising answers to common questions related to regulatory compliance and product development. Being articulate about your experiences will help you make a strong impression.
We think you need these skills to ace Regulatory Affairs Business Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Regulatory Affairs Business Specialist position. Understand the key responsibilities and required skills, such as knowledge of medical device regulations and experience in regulatory affairs.
Tailor Your CV: Customise your CV to highlight relevant experience in regulatory affairs, quality compliance, or product development within the medical device industry. Emphasise any specific tools you have used, like Rimsys or SAP, that are mentioned in the job description.
Craft a Compelling Cover Letter: Write a cover letter that connects your background and skills to the specific requirements of the role. Mention your understanding of regulatory compliance and how your previous experiences align with the company's objectives.
Highlight Communication Skills: Since excellent communication is crucial for this role, ensure that your application reflects your written and verbal communication abilities. Provide examples of how you've effectively managed multiple deliverables in past roles.
How to prepare for a job interview at Philips International
✨Understand Regulatory Affairs Basics
Make sure you have a solid grasp of the fundamentals of regulatory affairs, especially in the medical device industry. Familiarise yourself with relevant regulations and standards, as this knowledge will be crucial during your interview.
✨Showcase Your Communication Skills
As an excellent communicator, be prepared to demonstrate your written and verbal communication skills. You might be asked to explain complex regulatory concepts clearly, so practice articulating your thoughts succinctly.
✨Highlight Relevant Experience
Discuss any previous experience you have in regulatory affairs or quality compliance. Be specific about your roles and responsibilities, and how they relate to the position you're applying for. This will help the interviewers see your fit for the role.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities in regulatory contexts. Think of examples from your past experiences where you successfully navigated regulatory challenges, and be ready to share these stories.
