CrawlJobs Logo

Junior External Affairs Manager

Belgium, Leuven · Job Posted May 28, 2026
Apply Position
Job Link Share

Job Description

Within ASML, the Government & External Affairs (GEA) department is responsible for representing the company’s interests and ideas towards governments, institutions and business alliances and for shaping public policy and political decision-making in support of ASML’s strategic objectives and the communities we operate in. As Junior Advocacy Manager, you will support ASML’s engagement with European institutions and key Member States by contributing to the development and execution of advocacy strategies on technology, innovation, environment, and trade policy. Working closely with senior colleagues in Brussels and at HQ, you will help shape and draft positions and strategies, monitor EU and national policy developments, represent ASML in industry fora, and build trusted relationships with institutional and industry stakeholders to advance ASML’s strategic interests in Europe.

Job Responsibility

  • Support senior colleagues with the development and implementation of ASML advocacy strategies towards the European institutions and relevant Member States outside of the Netherlands
  • Support with the drafting and development of position paper and other advocacy related materials
  • Monitor and analyze relevant EU and Member States policy developments and report back to HQ and Brussels colleagues
  • Represent ASML in Trade associations and industry bodies
  • Develop and maintain a relevant network with industry and institutional stakeholders

Requirements

  • A Masters’ degree in a relevant field (political science, economics, law, international relations)
  • 2-3 Years experience in a relevant position with in-house interest representation, trade association or an (EU) institution
  • Professional proficiency in English is required.

Nice to have

  • German, French or an additional EU language are an asset
  • A proven track record in EU-level interest representation, or a strong interest in developing expertise in this area, particularly in technology, innovation or trade policy
  • Experience working across diverse topics is an asset
  • Experience navigating complex, cross-cutting topics is an asset
  • Experience in a corporate environment is an asset

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Junior External Affairs Manager

8 matching positions

Regulatory Affairs Manager (China)

Biocomposites is an international medical devices company that engineers, manufa...
Location
Location
China , Shanghai
Salary
Salary:
Not provided
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree in a life science or equivalent
  • Minimum 8 years’ experience within the medical device industry
  • Experience of pre-submission consultations with NMPA
  • Experience of medical device submissions to NMPA
  • Proven knowledge of medical device regulation and applicable standards and guidance documents in China
  • Fully proficient in both Chinese and English (written and oral)
  • Strong written and verbal communication skills with ability to convey matters clearly and to express complex issues in both English and Chinese
  • Exceptional teamworking skills
  • Strong sense of initiative and self-motivation
  • Excellent interpersonal and communication skills when liaising with internal and external stakeholders from varying disciplines and cultures
Job Responsibility
Job Responsibility
  • Lead the creation of submissions, registrations and medical device reporting for new and existing products in China (and other APAC territories as required)
  • Communicate with and coordinate consultants and regulators in China to plan, facilitate and execute consultation meetings, product applications and to maintain products on market
  • Develop strategies and plans to register products in China
  • Compile and maintain technical documentation for product registrations in accordance with Chinese and other specified country requirements
  • Prepare and review product documentation in the Chinese language
  • Lead the preparation and review of materials for pre-submission consultations with NMPA including briefing books and powerpoint presentations
  • Travel to NMPA and/or Test Laboratories to facilitate product registration as required
  • Research and consult on regulatory requirements to register new or changed products in China
  • Report, assess and communicate changes in regulations
  • Guide the organisation to maintain compliance with the latest NMPA law and regulations relating to medical devices
What we offer
What we offer
  • Competitive salary and benefits
  • We grow talent
  • One Biocomposites – team spirit & engagement
  • Fulltime
Read More
Arrow Right

GynOnc Clinical Trial Regional Medical Affairs Manager

The GynOnc Clinical Trial RMAM is responsible for the successful conduction of a...
Location
Location
Germany , Munich
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent)
  • At least 3 years experience in medical affairs, medical science liaison, clinical research or related industry role
  • Strong clinical and scientific knowledge relevant to the therapy area for the role
  • Excellent verbal and written communication skills in German and English
  • Willingness and ability to travel regularly within the assigned region
  • Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment
Job Responsibility
Job Responsibility
  • Lead and coordinate medical research activities on a local level to ensure high scientific and operational quality
  • Ensures that all clinical studies are planned, executed and communicated in line with regulatory standards and company objectives
  • Manage internal and external partners to ensure quality, timelines and budget are met
  • Develop regional omnichannel engagement plans, combining face-to-face and digital outreach to meet healthcare professional needs
  • Acting as a central interface between local and global Medical Affairs stakeholders, regional medical affairs managers, clinical development and clinical research organizations to ensure cross-functional collaboration
  • Plan and run regional medical activities such as advisory boards, symposia and educational meetings
  • Contributes to the generation of high-impact and robust data in clinical trials to inform treatment decisions, support product differentiation and improve outcomes for oncology patients
  • Mentor and support development of more junior medical colleagues
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Fulltime
Read More
Arrow Right

Non-Pharma Global Regulatory Affairs Manager

The Global Regulatory Sciences-Legacy Products-Non-Pharma Manager manages regula...
Location
Location
Italy , Bologna; Milano; Pomezia
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Proven experience in Regulatory Affairs within the pharmaceutical or life sciences industry, preferably within the food supplements, medical devices, and cosmetics sectors
  • Hands-on experience with regulatory submission processes, especially within EU and/or RoW markets or similar relevant experiences
  • Demonstrated ability to coordinate projects or deliverables with complexity and limited supervision
  • Advanced degree in Life Sciences, Pharmacy, Chemistry, or a related field
  • Good knowledge of global regulatory frameworks including EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
  • Strong organizational skills, attention to detail, and ability to manage priorities
  • Collaborative mindset and effective communication with team members and stakeholders
  • Ability to operate independently on clearly defined assignments
  • Proficiency in Microsoft Office Suite and regulatory submission/document management tools
  • Fluent in English, both written and spoken
Job Responsibility
Job Responsibility
  • Accountable for providing the necessary regulatory inputs in a cross-functional team for the development of new projects
  • Accountable for the execution and implementation of global regulatory strategies by managing day-to-day activities for assigned products
  • Manage multiple regulatory workstreams independently, including authoring, reviewing and coordinating documentation for regulatory submissions such as variations, renewals and geo-expansions
  • Provide and review regulatory assessments for change controls and product updates
  • Responsible for the preparation, review and collection of documentation for submission and maintenance of Technical File and PTD for the project assigned
  • Provide critical review of documentation supporting regulatory applications
  • Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
  • Contribute to the preparation and presentation of regulatory project updates in internal meetings and governance committees
  • Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
  • Support other relevant assignments as directed by supervisor
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
Read More
Arrow Right

Medical Affairs Oncology/Specialty Manager

Office-based activities: Develop and execute the medical strategy for GSK’s Onco...
Location
Location
Ukraine , Kiev
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Medical degree (MD), advanced scientific degree (PhD) with relevant oncology clinical experience is an advantage
  • 5–10+ years’ experience in Oncology Medical Affairs, clinical development, or related functions
  • Experience managing cross‑functional projects
  • Strong scientific credibility and clinical judgement
  • Strong verbal and written communication skills
  • ability to tailor complex scientific information to diverse audiences
  • Commitment to compliance and ethical engagement
  • Understanding of statistical design and analysis
  • Effective networking and collaboration skills with demonstrated ability to influence cross-functionally
  • Curiosity and commitment to continuous learning and professional development
Job Responsibility
Job Responsibility
  • Lead development and execution of the GSK Ukraine Medical Plan aligned to global medical strategy and local needs
  • Provide scientific and clinical expertise on Oncology/Specialty biology, treatment paradigms, and evolving data to internal teams (Commercial, R&D, Regulatory)
  • Oversee clinical trial strategy and investigator-initiated studies (IIS)
  • Drive medical affairs activities: congress strategy, symposia, advisory boards, and scientific materials for HCPs visiting
  • Leverage scientific expertise and market knowledge to identify and engage HCPs, including academic and community physicians, pharmacists, nurses, and other healthcare professionals, to assess educational needs
  • Engage with HCPs on emerging data, clinical trials, medical unmet needs, patient barriers to access, and market dynamics
  • provide disease-state and product-related scientific education in a non-promotional manner
  • Collect and communicate medical insights across the product lifecycle to contribute to medical strategy and understand the potential impact of these insights
  • Interpret and communicate clinical evidence to stakeholders
  • translate data into clinical and payer insights
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Fulltime
Read More
Arrow Right

Junior Regulatory Affairs Specialist

Junior Regulatory Affairs Specialist of Cosmo Intelligent Medical Devices.
Location
Location
Italy , Rome
Salary
Salary:
Not provided
cosmoimd.com Logo
Cosmo Intelligent Medical Devices
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in engineering, science or related scientific discipline, or equivalent
  • Minimum of 2 years of experience in regulatory affairs roles within the medical devices or healthcare industry
  • English proficiency at professional level
  • Professional knowledge of Reg. (EU) 2017/745 and Title 21 CFR parts 800-898 and technical standards ISO 13485, ISO 14971
  • Practical understanding of scientific and technological aspects related to software, computer engineering, artificial intelligence, and endoscopy
  • Strong analytical skills with a detail-oriented approach
  • Ability to work independently and collaboratively across multifunctional teams
  • Highly dynamic and adaptable to a fast-moving and innovative environment
Job Responsibility
Job Responsibility
  • Assess, prepare, and manage technical documentation to support certification and submission processes in the European Union and U.S.A
  • Prepare and manage technical dossiers for submission in other countries according to local regulations and guidance documents
  • Cooperate with other departments to the creation and update of technical documentation needed according to country requirements
  • Assist external stakeholders in the regulatory process per country requirements
  • Maintain and update certifications, registrations, and renewals as required by country regulations and assess regulatory impact of medical device changes with respect to country requirements
  • Cooperate to the management of documented material and communications with Competent Authorities, Certification Bodies, and other stakeholders according to the given regulatory aspect
  • Cooperate to the management of company regulatory procedures by timely awareness and implementation of changes due to the development in the regulatory landscape
  • Assist in internal and external audits and provide regulatory input to optimize company compliance and minimize the possibility of non-compliance findings
  • Promote the culture of compliance by proactively interacting with all departments and by provision of trainings
  • Cooperate to the development of new activities, adapt to new challenges and opportunities, and take on new duties stemming from the development path of company activities
Read More
Arrow Right

Senior Manager of Global Regulatory Affairs

A Senior Manager of Global Regulatory Affairs leads the development and executio...
Location
Location
United States , Deerfield
Salary
Salary:
136000.00 - 187000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or country equivalent in a scientific discipline
  • Minimum of 7-year experience in RA
  • Expert Regulatory knowledge
  • Sound basis of Scientific (Training/ Communications) knowledge
  • Management skills
  • Ability to oversee multiple projects in a matrix team environment
  • Excellent oral and written communication and presentation skills
  • Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
  • Technical and management skills
  • Ability to lead, coach, and motivate others
Job Responsibility
Job Responsibility
  • Serves as the Global Regulatory Lead for Baxter’s hemostat and sealant product(s) registered as biologic/combination products
  • Provide technical and strategic input for regulatory decisions aligned with business strategy
  • Identify & prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups
  • Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards
  • Assess impact of new regulations and provide feedback
  • Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks
  • Act as primary contact for meetings with regulatory authorities including planning and leadership
  • Maintain appropriate communication within the RA function, with Global Marketing, and with other functions primarily at the project team level
  • Plan and manage complex projects and prioritize workload
  • Initiate, manage and maintain operational activities in support of new and existing marketing authorizations
What we offer
What we offer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Fulltime
Read More
Arrow Right

Senior Manager of Global Regulatory Affairs

A Senior Manager of Global Regulatory Affairs leads the development and executio...
Location
Location
United States , Deerfield
Salary
Salary:
136000.00 - 187000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree or country equivalent in a scientific discipline
  • Minimum of 7-year experience in RA
  • Expert Regulatory knowledge
  • Sound basis of Scientific (Training/ Communications) knowledge
  • Management skills
  • Ability to oversee multiple projects in a matrix team environment
  • Excellent oral and written communication and presentation skills
  • Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
  • Technical and management skills
  • Ability to lead, coach, and motivate others
Job Responsibility
Job Responsibility
  • Serves as the Global Regulatory Lead for Baxter’s hemostat and sealant product(s) registered as biologic/combination products
  • Provide technical and strategic input for regulatory decisions aligned with business strategy
  • Identify & prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups
  • Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards
  • Assess impact of new regulations and provide feedback
  • Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks
  • Act as primary contact for meetings with regulatory authorities including planning and leadership
  • Maintain appropriate communication within the RA function, with Global Marketing, and with other functions primarily at the project team level
  • Plan and manage complex projects and prioritize workload
  • Initiate, manage and maintain operational activities in support of new and existing marketing authorizations
What we offer
What we offer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Fulltime
Read More
Arrow Right

Manager - Labeling

As part of GLC group, and under the supervision of the Global Labeling Process M...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s/Master’s degree with minimum 8 years of experience in Labeling
  • Previous experience working in industry in support of End to End Labeling Initiatives including global labeling compliance and regional labeling for international (ROW) markets
  • Oral and Written Communication and Presentation Skills
  • Project Management skills such that candidate can work independently to deliver expected outputs
  • Relationship Management
  • Influencing, Negotiation and Decision Making Skills
  • Extends capabilities by working closely with senior staff/experts within and outside the internal organization
  • Previous labelling experience in HA Regulations and International Markets
  • Knowledge of labelling regulations and requirements, industry trends and business principles
  • Demonstrates leadership attributes, managing individual and complex group projects
Job Responsibility
Job Responsibility
  • Apply expert labeling knowledge to collaborate with Local Amgen Affiliates, along with Regional Regulatory Affairs and Operations colleagues, to plan and implement label changes, ensuring compliance with labeling processes
  • Provide process and system support
  • Provide artwork source text and process support as necessary
  • Participate in Labeling Submissions meetings to provide input on labeling processes
  • Provide regional operational support for labeling
  • Support document management of all regional labeling documents, source text, illustrations, and related documents
  • Support the maintenance of business process documentation, including guidance documents
  • Provide accurate regulatory assessments for Change Control records governing the implementation of labeling changes
  • Maintain a state of inspection readiness for records within the Labeling tool
  • Develop regional package component labels according to regulations and company guidelines
  • Fulltime
Read More
Arrow Right