Regulatory Affairs Intern Job at BD (Tempe)

Regulatory Affairs Intern

The RA Intern provides support for a variety of Regulatory Affairs activities re...

Location

United States , Tempe

Salary:

Not provided

BD

Expiration Date

Until further notice

Requirements

High school diploma or equivalent required
Currently enrolled in an undergraduate or graduate school program, or recent graduate
Ability to plan and schedule multiple priorities in a concurrent fashion
Ability to review, collate and summarize scientific and technical data
Good problem solving and analytical skills
Good written and oral communication skills
Ability to work in a regulated environment

Job Responsibility

Provide general RA support for regulatory projects, under the direction of an RA professional
Effectively manage multiple competing priorities
Assist with the collection of project related documentation and assist with preparation of regulatory submissions
Liaise with the subject matter experts to collect information and communicate with the team members
Assist in auditing, editing and publishing of regulatory submissions as appropriate
Work across full suite of Microsoft office software programs, Adobe, and multiple internal software programs/databases

Intern - Regulatory Affairs

Intern - Regulatory Affairs at Ecolab in Kraków, Poland. Ecolab is a global lead...

Location

Poland , Kraków

Salary:

Not provided

Edgerton Dental Clinic

Expiration Date

Until further notice

Requirements

Student status in a chemistry or biology related field
Knowledge of REACH and CLP regulations is an asset
Strong command of Excel
Well‑developed analytical skills
Minimum 20h/week
>B1 level in English

Job Responsibility

Completing certification forms related to the Kosher and Halal processes for the company’s product portfolio
Collaborating with the Trade Compliance team to support order release activities and ensure adherence to all applicable regulations
Entering and updating data in the SAP system in line with the department’s current operational needs

What we offer

Onsite training giving you the opportunity to learn, grow and shape your career
Lunch subsidy for our onsite canteen or catering
Social events such as family events, charity auctions
Comfortable working environment (Library, relaxation area, casual dress code, air purifiers)
Possibility to work in a hybrid model

Parttime

Governmental & Regulatory Affairs Intern

Internship within the Regulatory Affairs team, which supports business operation...

Location

United States , Las Vegas

Salary:

Not provided

UFC

Expiration Date

Until further notice

Requirements

Currently enrolled in a Bachelor’s or Graduate degree program in a relevant field such as Legal Studies, Sports Management, Business, Public Policy, or a similar discipline
Junior, Senior, or Graduate-level standing preferred
Ability to organize information and support the presentation of analysis and concepts
Ability to handle confidential information with discretion and professionalism
Strong organizational skills with a high level of attention to detail
Working knowledge of Microsoft Office programs: Word, Excel, PowerPoint, and Outlook, with the ability to learn additional systems
Eager to learn, take initiative, and grow in a fast-paced environment

Job Responsibility

Maintain and organize digital and physical regulatory records, including printing, scanning, and filing documentation
Assist with managing and reviewing Commission Officials’ credentials in advance of upcoming events
Support the updating and maintenance of regulatory-related spreadsheets and tracking tools
Participate alongside Regulatory team members in advance event preparation calls with Athletic Commissions
Collaborate with internal departments to help ensure alignment and understanding of event-specific rules and regulatory requirements
Support the Regulatory team on additional projects and administrative tasks as needed

What we offer

Paid internship
Hands-on experience and exposure to the global sports and entertainment industry
Participation in events such as welcome/farewell sessions, a speaker series featuring company leaders, and career training workshops addressing everything from LinkedIn profile enhancement to resume building, interviewing skills, and networking

Fulltime

Regulatory Affairs Consultant- Regulatory Partner Responsible

As part of Parexel Consulting, you will play a vital role in helping biopharmace...

Location

India , Bengaluru

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Ideally 5+ years of experience in Regulatory Affairs, oversight, governance or compliance roles within pharmaceutical, biotechnology or healthcare industry
Partner management experience: proven experience in managing relationships with third-party vendors
Ability to work in a highly matrixed organization and to establish successful cross-functional working relationships with people in a wide variety of disciplines and backgrounds, be interpersonally aware and culturally sensitive

Job Responsibility

Ensure oversight on key processes and ensure framework is in place to manage third-party activities E2E ensuring compliance with regulations and company standards
monitor partner performance against agreed-upon metrics and standards, addressing any deviations or deficiencies promptly
Conduct periodic assessments of partners to ensure compliance with local requirements and quality standards, implement corrective actions as necessary
develop risk mitigation strategies and implement controls to minimize risks associated with partner activities. Act as point of contact for escalations and issue resolution related to partner activities
Stay updated on local regulatory requirements, guidelines, and industry trends to ensure compliance with evolving regulations and communicate to GRA and local team
participating in policy activities with industry groups and trade associations
Support regional regulatory TA teams within GRA, for efficient planning and submission preparation according to local requirements and business needs
Keep internal databases up to date with local activity and ensure compliance KPIs are adequately kept on track
Act as primary interface with local partners representing the company's regulatory interests and fostering positive relationships and ensure that partner, who is acting on CSL behalf, has the appropriate interactions with Has
Monitor training effectiveness and compliance, ensure proper trainings are developed and in place, providing support and resources as needed to address gaps and improve performance

What we offer

Flexible work arrangements

Senior Regulatory Affairs Consultant - Regulatory Intelligence

As part of Parexel Consulting, you will play a vital role in helping biopharmace...

Location

United States , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

At least 5-7 years of regulatory affairs experience to include previous regulatory intelligence experience
Knowledge of FDA regulations as well as an understanding of the Summary basis of approval and labeling is helpful
A minimum of a bachelor’s degree in a scientific or technical discipline, advanced degree preferred
Project management / leadership experience
Excellent interpersonal and intercultural communication skills, both written and verbal
Client-focused approach to work (Quality)
Results orientation
Teamwork and collaboration skills
Consulting skills
Critical thinking and problem-solving skills

Job Responsibility

Regularly search the public domain for new and updated regulations and regulatory guidance documents that can impact the client’s development programs, and report the most critical findings
Regularly search the public domain for competitor product regulatory developments and report the most critical findings
Inform client immediately of any changes to the regulatory environment directly affecting client’s business
Search for non-compliance letters or notices for client’s suppliers and provide a regular report
Perform ad hoc research on specific regulatory topics at client’s request, using the internet and various subscription database tools
Identify public commenting opportunities for draft guidances/regulations and coordinate review and comments from client. Lead the client’s internal process to obtain and coordinate SME impact assessments/comments, facilitate comment collection/assimilation, and help develop company messaging to share either with PhRMA working groups or directly with Health Authorities.
Maintain a list of upcoming regulatory meetings/workshops/conferences pertinent to client
Support Regulatory Intelligence activities, including the use of Cortellis, Citeline, WebWatcher. This includes tracking, coordinating and participating in ad hoc searches as well as scheduled activities.

What we offer

Flexible work arrangements
Opportunities for career growth
Supportive and inclusive environment
Diverse and global client exposure
Learn from experts

Senior Counsel, Regulatory Affairs

The Legal Team for Mastercard Payment Services is looking for a Senior Regulator...

Location

Norway , Oslo

Salary:

Not provided

Mastercard

Expiration Date

Until further notice

Requirements

Experience as a lawyer in reputable Norwegian law firms and/or in-house counsel in Norway
Ability to establish overview of complex regulatory matters and identify impact on our services or internal organization
Experience with, or interest in, financial services regulation with emphasis on technology infrastructure, operational resilience and third-party risk management and outsourcing regulation, including the EU Digital Operational Resilience Act and local Norwegian national security regulation in respect of digital infrastructure. Experience from similar infrastructure related areas will also be relevant
Experience with and/or interest in data privacy law is an advantage but not a requirement
Ability to think and act both strategically and tactically with respect to the needs of business clients and their objectives while ensuring that the we remain compliant with existing regulatory obligations, react to regulatory threats and opportunities, and maintain good working relationships with key regulators
Language requirements: Fluent in Norwegian (written and spoken). Fluent in English
Law degree required
Ability and willingness to take project management responsibility for regulatory driven processes

Job Responsibility

Providing legal advice and guidance on Norwegian regulatory matters, with a particular focus on the payments and financial services landscape
Supporting the commercial law function, especially in relation to contractual aspects and related legal documentation
Providing advice and guidance on regulatory and data privacy matters in respect of Mastercard’s services
Supporting customer and regulator engagement materials, updates, reports and presentations
Engagement with internal stakeholders in the business and the Risk, Commercial Law and Privacy teams
Negotiating data processing agreements with customers, suppliers and other relevant parties
Assisting the MPS business in relation to maintaining up-to-date processing records
Providing privacy advice to the business on an on-going basis
Assisting in drafting, reviewing, and interpreting contract clauses related to direct or indirect regulatory and data privacy requirements
Participating in negotiations related to the same

What we offer

5 annual Volunteer Days
MPS Active for running training, yoga, cycling, football and more

Fulltime

Regulatory Affairs Specialist

Are you a tech-savvy scientist with a passion for food law and innovation? A lea...

Location

Belgium , Leuven

Salary:

Not provided

Randstad

Expiration Date

September 06, 2026

Requirements

Undergraduate or Master’s degree in a relevant scientific or technical field, including coursework or exposure to food law
A minimum of 3 years in an SRA or R&D role, with hands-on experience working with legislation and its commercial application
Strong understanding of Global Food Law (interpretation and application)
Ideally possesses laboratory experience interpreting scientific data and technical reports
A background in nutrition, novel food regulations, or GRAS frameworks—particularly regarding functional ingredients, safety assessments, and health claims—is a major plus
Exceptional communication and influencing skills, a proven track record of perseverance and agility, and the ability to work under pressure against tight deadlines
Full fluency in English is required (other languages are an advantage)
Willingness to travel globally up to 20% of the time

Job Responsibility

Provide Global Regulatory Advice: Deliver expert guidance that optimizes commercial opportunities across multiple international markets while preserving the company’s reputation
Support Innovation & Tech Projects: Lead SRA insights for complex, high-priority commercial and technical projects, ensuring they meet business demands on time and within budget
Bridge Cross-Functional Teams: Promote synergies across global zones, connecting technical, marketing, and legal teams to develop compliant yet competitive business solutions
Analyze Market Trends & Science: Monitor consumer insights, emerging science, and competitor strategies to translate global regulatory assessments into actionable business scenarios for stakeholders
Leverage Global Networks: Work closely with the wider SRA network to optimize ways of working and deliver consistent, integrated recommendations

Fulltime

Corporate Affairs Intern

Location

Paris

Salary:

1200.00 - 1400.00 EUR / Month

Mirakl

Expiration Date

Until further notice

Requirements

Currently pursuing a Master's degree (Bac+5) in Communications, Public Affairs, or Political Science from a business school, Sciences Po, or university
First hands-on experience in press relations, institutional communications, and/or public affairs (internship or apprenticeship)
Genuine passion for e-commerce, digital transformation, and the platform economy
Exceptional written and verbal communication in both French and English
Strong organisational skills with the ability to manage multiple projects simultaneously
Research and analytical skills for regulatory and media monitoring
Sharp attention to detail and high editorial standards
Collaborative mindset, comfortable working in an international and fast-paced environment
French: Native / C2 level required
English: C2 level required

Job Responsibility

Drive Mirakl's media presence by crafting press releases and institutional content, preparing press briefings, tracking media coverage, and coordinating with our PR agencies across France and Europe
Support executive communications by preparing public speaking materials, key messages, and Q&A documents for Mirakl leaders' institutional appearances and events
Strengthen Mirakl's public affairs strategy through regulatory monitoring (e-commerce, AI, platform economy) and contributing to the drafting of position papers and advocacy materials
Build and nurture relationships with public stakeholders — engaging with MPs, senators, ministerial offices, and European institutions through institutional meetings and events
Create and curate institutional social media content in French, ensuring editorial quality and alignment with the marketplace editorial calendar

What we offer

50% reimbursement of public transport costs
Ticket Restaurant card
Join a vibrant intern & apprentice community: #MiraklInterns

Select Country

Regulatory Affairs Intern

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?