CrawlJobs Logo

Regulatory Affairs Training Manager

srgtalent.com Logo

SRG

Location Icon

Location:
United Kingdom , White City, London

Category Icon
Category:
-

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

SRG are looking for RA training manager to join a global pharmaceutical company based in London. The RA Training Manager - RIM will have a key role in the success of continued Veeva RIM roll-out and implementation within the companies RA, supporting Organisational Change Management (OCM) training activities as a core SME and ensuring RA staff have access to fit-for-purpose training material. In alignment with the Functional Change Lead, the RA Training Manager - RIM will be responsible for the training plan creation and management, contribute to the design of training approach, prepare training materials, and organise training development; training coordination and delivery to Super Users and End Users. You will also be responsible for maintaining the training materials post Go live.

Job Responsibility:

  • Review and validate central Training material related to Veeva RIM platform deployment
  • Create any local Function-specific materials as required, especially for Super Users
  • Ensure training materials are regularly updated for program changes (incl. Job aids, e-learnings, etc)
  • Set up any mandatory e-Learning content training in Up4Growth for training push
  • Customize Training communications material from Central Training team to provide proactive information and regular updates
  • Contribute to creating and delivering Function-specific Training communications and materials as necessary, in line with agreed central governance processes
  • Support coordination and promotion of Show & Tell/ demo sessions within Function
  • Attend central Train the Trainer sessions
  • Schedule Super User training sessions in Up4Growth
  • Deliver Training sessions
  • Generate Up4Growth Super User Tracking reports
  • Schedule End User Instructor-Led training sessions in Up4Growth, leveraging Function End User lists
  • Deliver Training sessions
  • Support Super Users during their own training sessions to End Users (tech and content support)
  • Provide support to End Users throughout the training period
  • Generate Up4Growth End User Tracking reports
  • Track actual Attendance Report and compile End User Completion Reports
  • Ensure all Function associates achieve training pass, and any other approvals required in order to secure Veeva access authorisation
  • Ensure Functional business roles are correctly mapped to correct system roles and permissions
  • Help to raise Functional Training-related risks, issues, and change requests as required via appropriate channels, ensuring Central OCM team visibility
  • Regularly connect with Functional stakeholders to understand and mitigate concerns
  • Liaise with Veeva Product Owners to understand release impacts (x3 per year) on existing system, processes, and ways of working
  • Identify key affected audiences
  • Conduct impact assessment on existing training materials
  • Revise, retire or create new materials and job support tools that reflect release changes
  • Plan and execute training delivery strategies to key impacted audiences
  • Schedule, communicate and deliver training as needed
  • Evaluate training effectiveness
  • Assess for effective adoption of release changes, preparing further supports, if needed

Requirements:

  • Life Science Degree or other University degree with equivalent experience
  • Strong training, communications, project management skills
  • Experience in Project management tools & systems
  • Proven successful experience on the design and development of training concepts with cross-functional teams
  • Strong training delivery capability
  • Good understanding and direct experience with Veeva RIM deployments
  • Good understanding of all RA roles
  • Good Organizational awareness
  • Technology-savvy - ability to leverage and use systems, technology and automation to (including digital assistants and AI tools) to derive impactful trainings and communications
  • Strong communication skills

Additional Information:

Job Posted:
January 19, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Regulatory Affairs Training Manager

Pharmacovigilance and regulatory affairs manager BeNeLux

Responsible for overseeing Regulatory affairs and Pharmacovigilance activities a...
Location
Location
Netherlands , Utrecht
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 5-10 years of experience in regulatory affairs and pharmacovigilance within pharmaceutical company
  • Knowledge of local pharmaceutical legislation for Regulatory in the BeNeLux region
  • Knowledge of applicable laws and regulations to ensure full compliance
  • Knowledge of Regulatory affairs and Pharmacovigilance activities (act as primary contact for regulatory authorities and for external consultants in the regions, ensuring compliance of Product Information, API, approval of artworks for packaging materials and implementation of aRMM)
  • Proficiency in speaking, comprehending, reading and writing Dutch is required
  • Proficiency in speaking, comprehending, reading and writing English is required
  • Ability to think strategically & execute tactically
Job Responsibility
Job Responsibility
  • Act as local single point of contact for global functions in Regulatory Affairs and Pharmacovigilance for the BeNeLux
  • Act as the Local Safety Officer (LSO) for the Netherlands, Belgium and Luxembourg
  • Act as primary contact for regulatory authorities and for external consultants, ensuring compliance of Product Information, approval of artworks for packaging materials and implementation of aRMM
  • Responsible for creating and keep the local Regulatory affairs and Pharmacovigilance SOPs up to date
  • Responsible for training of BeNeLux team in local Regulatory affairs and Pharmacovigilance SOPs
  • Work closely together with Pharmacovigilance and regulatory affairs managers within the BNS cluster (BeNeLux Nordics and Switzerland) creating a network of knowledge and international cooperation and support
  • Collaborate with commercial, medical and market access to realize cross-functional objectives
What we offer
What we offer
  • Competitive salary and benefits package
  • Opportunities for professional growth and development
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

Employee in quality management and/or regulatory affairs

As a professional QM/RA associate, you will be responsible for tasks in Quality ...
Location
Location
Austria , Salzburg
Salary
Salary:
Not provided
brainlab.com Logo
Brainlab
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience or training in Quality Management, preferably in the medical device sector (ISO 13485) or any industry with high regulatory standards
  • Knowledge of EU MDR (Medical Device Regulation) and experience with Class II or higher medical devices is an advantage
  • Familiarity with clinical evaluations and post-market surveillance processes under MDR guidelines is highly desirable
  • Knowledge of international regulations and certifications for medical devices is a plus
  • Fluent in German and English (written and spoken)
  • Flexible, team-oriented, and eager to work in an international environment
Job Responsibility
Job Responsibility
  • Support and collaborate across all areas of Quality Management (QM)
  • Ongoing control, improvement, and optimization of quality management processes and standards
  • Assist in creating and reviewing deviation reports, risk management plans, and CAPA (Corrective and Preventive Actions), ensuring thorough monitoring of corrective actions
  • Ensure the implementation and monitoring of regulatory requirements for medical devices
  • Assist with international product certifications and approvals
  • Liaise with regulatory bodies and authorities, including correspondence with notified bodies (globally)
  • Support clinical evaluations, ensuring that medical devices meet clinical safety and performance requirements in accordance with regulatory standards
  • Participate in post-market surveillance activities, including monitoring product performance in the market and managing feedback loops to continuously improve device safety and effectiveness
  • Support internal and external audits as well as supplier audits
  • Assist R&D with documentation and support the development process
What we offer
What we offer
  • A motivating work atmosphere in a young, dynamic team
  • An exciting and varied scope of assignments customized for your skills and interests
  • The opportunity to grow with us, be directly involved and participate in our company’s success
  • A secure, permanent full-time contract
  • Generous social benefits within our culturally diverse enterprise
  • Freshly-cooked meals and healthy snacks provided daily
  • Good public transport connections and parking facilities available
  • Flexible working hours
  • Support for daily obligations (childcare, etc.)
  • Fulltime
Read More
Arrow Right

Regulatory & Compliance Manager

Location
Location
Egypt , Cairo
Salary
Salary:
Not provided
paxerahealth.com Logo
PaxeraHealth
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in compliance, regulatory affairs, business administration, or related field
  • At least 3-5 years of experience in compliance, regulatory management, or quality assurance, ideally within the healthcare or software industry
  • Strong knowledge of industry regulations, quality standards (ISO), and compliance processes
  • Experience with obtaining ISO 9001, ISO 27000, ISO 13485, FDA, MDR
  • Excellent English Language
  • Excellent organizational, leadership, and communication skills
  • Ability to manage multiple projects and deadlines in a fast-paced environment
Job Responsibility
Job Responsibility
  • Oversee all aspects of compliance with regulatory requirements, industry standards, and internal policies
  • Lead efforts to obtain and maintain certifications (e.g., ISO 9001, ISO 27000, ISO 13485, FDA, MDR, and other relevant quality/compliance standards)
  • Ensure ongoing adherence to all applicable regulations, proactively identifying and addressing areas for improvement
  • Review, update, and maintain all regulatory files and documentation, ensuring timely submissions and filings
  • Monitor and interpret changes in laws, regulations, and industry standards
  • advise management on compliance implications
  • Implement and manage the company’s Quality Management Systems (QMS)
  • Collaborate with operations, product, and other teams to ensure products, services, and processes meet compliance and quality benchmarks
  • Conduct regular internal audits and assessments to evaluate compliance and certification readiness
  • Drive continuous improvement in quality processes through monitoring, feedback, and corrective action
  • Fulltime
Read More
Arrow Right

Non-Pharma Global Regulatory Affairs Specialist

The Global Regulatory Non-Pharma Specialist manages regulatory documentation and...
Location
Location
Italy , Bologna
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 5 years’ experience in Regulatory Affairs preferably within the food supplements, medical devices, and cosmetics sectors
  • Exposure to regulatory operations or documentation in EU and/or RoW markets or similar experiences is preferred
  • Advance degree in Life Sciences, Pharmacy, Chemistry, or a related field
  • Relevant certifications in Regulatory Affairs are considered a plus
  • Good knowledge of EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
  • Strong attention to detail, time management and organizational skills
  • Willingness to learn and ability to work effectively in a team-based environment
  • Strong communication and interpersonal skills
  • Proficiency in Microsoft Office Suite and familiarity with document management systems
  • Fluent in English, both written and spoken
Job Responsibility
Job Responsibility
  • Contributing in a cross-functional team to provide the necessary regulatory input for the development of new projects
  • Support regulatory strategies by providing impact assessments
  • Collaborate actively with the Research & Development team to integrate regulatory requirements during the design and development of assigned products
  • Prepare, organize and submit regulatory documentation for submission and maintenance of dossiers for the projects assigned
  • Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
  • Manage multiple tasks in a fast-paced environment while keeping on task and to the company’s quality standards
  • Contribute to the preparation of regulatory project updates in internal meeting and governance committee providing regulatory input and flagging risks
  • Assist colleagues with administrative tasks
  • Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
  • Review and validate commercial artwork, packaging, and labeling in compliance with EU Regulations, ensuring timely product launches
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
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

External Affairs Manager

Join us as an External Affairs Manager and play a pivotal role in shaping MDPI’s...
Location
Location
Singapore , Singapore
Salary
Salary:
Not provided
mdpi.com Logo
MDPI
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree and above
  • Minimum 5 years of experience in Public Affairs or Public Relations, with strong exposure to external communications and strategic initiatives
  • Minimum 2 years of managerial experience
  • Proven APAC regional experience, with the ability to work independently and hands-on across multiple markets
  • Demonstrated experience engaging with government stakeholders
  • Excellent command of English
  • proficiency in additional APAC languages would be a plus
  • Proficient in Microsoft 365
  • Attention to detail, confidence in stakeholder engagement, proactiveness, teamwork, and effective problem-solving
  • Ability to support corporate branding initiatives (e.g., Institutional Open Access Program) and deliver in-house training on communication strategy
Job Responsibility
Job Responsibility
  • Determine and manage the development and implementation of an External Affairs communications team and program in the Asia-Pacific region in line with MDPI’s mission and business goals
  • Manage public affairs and public relations activities across a portfolio of focus countries, liaising with Office/Operating Managers to cover policy matters, media relations, and broader reputational risks and opportunities
  • Provide strategic support to country representatives and spokespeople and manage stakeholder engagements
  • Manage and own EA resourcing for the APAC region, including team development and growth, campaign budgets, and agency requirements
  • Implement PR campaigns to enhance MDPI’s brand visibility across focus countries in APAC, focusing on academic, scientific, and policy-related media
  • Secure high-quality earned media coverage in top-tier and trade outlets across the region, with tailored messaging for each country market
  • Localize global narratives and campaigns to suit the cultural, linguistic, and sectoral nuances of key countries
  • Build and maintain strong relationships with journalists, editors, and media stakeholders in science, academia, education, and research policy
  • Coordinate with global teams to align regional communications with overall brand and publishing strategies
  • Provide strategic counsel and training to MDPI representatives in APAC
What we offer
What we offer
  • Professional and personal development
  • An international work environment
  • Flexible working hours in the limits of a full-time job
  • Business trips to the other MDPI offices
  • Competitive salary, benefits
  • Fulltime
Read More
Arrow Right

Manager, Medical Affairs

The Manager, Medical Affairs will provide clinical development and technical kno...
Location
Location
United States , Skaneateles Falls
Salary
Salary:
120000.00 - 165000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 5 years of related clinical experience required
  • industry experience preferred
  • Degree in related clinical field (Advanced Degree Preferred) or proven experience required
  • NP/PA/MD with primary and/or acute care experience such as ER, Urgent Care, or Hospitalist/internal medicine is ideal
  • Optometrist who displays sophisticated knowledge of physical assessment will be considered
  • Medical Affairs proven experience highly preferred
  • Active license in a U.S. state or territory in standing required with clinical expertise
  • Excellent written, verbal communication, and organizational skills
  • Effective and proficient presentation and teaching skills
  • Self-motivated, multi-tasking, with outstanding follow through
Job Responsibility
Job Responsibility
  • Serve as the medical and device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, and complaints
  • Provide accurate, balanced and timely clinical expertise to functional areas such as clinical development, R&D, marketing, manufacturing, quality assurance, regulatory affairs, and legal based on objective evidence and clinical experience
  • Provide clinical expertise for creation and development of risk assessments and quality standards for product design history files
  • Devise novel approaches to address clinical and technical problems in clinical practice through development and modification of related medical devices
  • Assimilate voice of customer and clinical experience for design input with new product development and product lifecycle management
  • Develop and deliver relevant medical device training programs that support product implementation, training, and marketing efforts
  • Train internal customers on product application, disease states, and regional differences as required
  • Support product implementation process creation, maintenance, and controlled launch when applicable
  • Maintain familiarity of published literature as objective evidence for clinical trends and therapies related to impact on product lines
  • Coordinate with other Medical Partners as needed to support Division Medical efforts
What we offer
What we offer
  • Medical and dental coverage starting on day one
  • Basic life, accident, short-term and long-term disability insurance
  • Business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan with 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
  • Fulltime
Read More
Arrow Right