New · posted Nov 6
Philips · Medical Devices
Intern - Regulatory Affairs
- Orlando, FL
- On-site
- Internship
- Associate & Specialist
The role
Intern – Regulatory Affairs
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 role.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Orlando FL.
What you need
You're the right fit if
- You are pursuing a BS in regulatory affairs, regulatory science Public Health, health Science or Engineering or equivalent.
- Strong planning and organization skills & effective written and verbal communication skills
- Effectively builds and manages relationships, partners and networks within the organization
- Is effective at executing independent and interdependent tasks and activities and is effective at interacting with middle & senior management
- You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position.
Skills named in this posting
- Pursuing BS in regulatory affairs, regulatory science, public health, health science or engineering
- Regulatory documentation compilation and review
- Product registration support
- Regulatory intelligence
- Technical documentation review
- Planning and organization
- Written and verbal communication
- Relationship building
What you'll do
In this role you
Are you interested in an Internship opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate BS to participate in 3 month paid intern opportunities at our site in Orlando, FL. Through this role you will gain meaningful, hands-on experience working for a HealthTech company.
Your role
- Provide regulatory support to cross-functional teams; identify opportunities for improving processes that cut across multiple functions and that have a tangible impact on business performance
- Compile & review the necessary local/in‐country documentation for relevant stakeholders to complete registration activities
- Follow up as needed with internal/external authorities to successfully notify/register products and confirm status of registration activities
- Work with team members on regulatory intelligence & regulatory topics to support stakeholders
- Review Technical Documentation & perform verification activities & support submissions
Pay and benefits
$49,920 – $60,320 a year
Employer provided$24.00 – $29.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesPhilips Transparency Details
The pay range for this position in Orlando FL is $24 to $29 Hourly.
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.
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.
Paid internship
Where you'll work
Orlando, FLOn-siteOpen in Maps (opens in a new tab)
More jobs in Orlando, FLWorking conditions
Job Title
Intern-Regulatory Affairs-Orlando, FL-Summer 2027
From the posting
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.
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.
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.
Job intelligence
The context around this role
Live data · November 6, 2026
Salary intelligence
How the pay compares
This role's midpoint is 39% below the US median for Regulatory Affairs roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US28 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $49,920 | — | $60,320 |
| All US (middle half) | $82,500 | $90,000 | $95,000 |
This role: Philips's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, November 6, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory Affairs
The general path across 177 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not Philips's own promotion track.
Career resources on Regulatory Affairs
Skills DNA
What this role leans on
How many of the posting's 15 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership5
- Documentation and SOPs2
- Regulatory submissions1
- Quality systems and risk1
- Pursuing BS in regulatory affairs, regulatory science, public health, health science or engineering
- Regulatory documentation compilation and review
- Product registration support
- Regulatory intelligence
- Technical documentation review
- Planning and organization
- Written and verbal communication
- Relationship building
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Regulatory Affairs work in medical devices, each linked to the agency or standards body that publishes it.
- FDAFDA 510(k)(official source, opens in a new tab)Premarket notification: showing substantial equivalence to a legally marketed device
- FDA21 CFR Part 814(official source, opens in a new tab)Premarket approval of class III medical devices
- FDAFDA De Novo(official source, opens in a new tab)Classification requests for novel low- to moderate-risk devices
- FDAFDA Q-Submission Program(official source, opens in a new tab)Pre-Submissions and meetings with FDA on device submissions
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- FDAFDA eSTAR(official source, opens in a new tab)The electronic submission template for 510(k) and De Novo requests
- EUEU IVDR (Regulation 2017/746)(official source, opens in a new tab)The EU In Vitro Diagnostic Medical Devices Regulation
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 812(official source, opens in a new tab)Investigational device exemptions for clinical studies of devices
- FDA21 CFR Part 807(official source, opens in a new tab)Establishment registration, device listing and premarket notification
- FDA21 CFR Part 801(official source, opens in a new tab)FDA labeling requirements for medical devices
- EUMDCG guidance(official source, opens in a new tab)The Medical Device Coordination Group's endorsed guidance on applying the MDR and IVDR
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- Health CanadaCanada Medical Devices Regulations(official source, opens in a new tab)Health Canada's licensing and quality requirements for medical devices (SOR/98-282)
Company hiring pulse
Philips on Regulatory Jobs
- 33
- Open roles
- 33
- Distinct roles
- 14
- Locations
By discipline
- Quality26 79%
- Clinical4 12%
- Regulatory3 9%
By level
- Senior & Principal14 42%
- Associate & Specialist9 27%
- Manager7 21%
More roles at Philips
- View role
Clinical Scientist – Computed Tomography
Orange, OHSenior & PrincipalMedical Devices$101K–$162K
- View role
Senior Clinical Scientist – Computed Tomography
Rochester, MNSenior & PrincipalMedical Devices$139K–$223K
- View role
Clinical Affairs Director
Orange, OH +2 more · HybridDirectorMedical Devices$171K–$306K
- View role
Senior Clinical Development Scientist / Medical Safety Manager
Bothell, WA · HybridSenior & PrincipalMedical Devices$149K–$237K
Similar Regulatory Affairs roles elsewhere
- View role
Regulatory Affairs Specialist
DanaherIrvine, CAAssociate & SpecialistMedical Devices$80K–$100K
- View role
Regulatory Affairs Specialist I
Cook MedicalBloomington, INAssociate & SpecialistMedical DevicesSalary not listed
- View role
Regulatory Affairs Specialist II
Cook MedicalVandergrift, PAAssociate & SpecialistMedical DevicesSalary not listed
- View role
Regulatory Affairs Specialist II – Lingo
AbbottAlameda, CAAssociate & SpecialistMedical Devices$82K–$141K
Intern - Regulatory Affairs at Philips
Applications close November 13. $50K–$60K a year, employer provided.