Overview
We are looking for an enthusiastic Regulatory Affairs Submission Manager to join our dynamic Adalvo team. This position offers an opportunity to well-suited candidates to join a growing, fast-paced energetic environment and culture.
At Adalvo, we’re not just a company – we’re a team of passionate people driven by our mission to consistently deliver high-quality products and services to our partners. We are positive, fast, and we are always on target , we are Adalvo !
Responsibilities
- Initiating, coordinating and supervising the registration of medicinal products through European procedures (MRP, DCP, CP) or national submissions across all regions of interest
- Devising submission strategy for each project, in line with all applicable requirements, and assign due dates
- Directing and coordinating preparation of document packages for regulatory submissions, in line with the in force European regulations and / or local pharmaceutical laws depending on the submission type and market
- Ensuring that all responses to authorities’ requests are correct, complete and timely provided
- Communicate with third parties to expedite submissions and ensure regulatory compliance
- Ensure that all the additional processes related to national submissions (pre-reviews, DMF, PMF, GMP accreditation etc.) are provided on time and that their submission / approval process does not delay the application
- Ensure that accurate and complete information is timely provided to other departments / third parties
- Provide support for samples preparation and dispatch, when necessary
- Inform the relevant functions on the status and progress of assigned projects to meet the set objectives, identify potential problems or delays, and possible solutions, as they occur
- Compile, verify and publish submissions using electronic publishing software considering the submission deadlines and technical requirements on management of dossiers lifecycle
- Documenting and tracking regulatory related processes within the organisation
- Ensure that the internal trackers and dedicated templates are kept up-to-date
- Perform regular reviews of the information available on the internal SP
Candidate Requirements
5+ years of experience in regulatory affairs with a focus on submissions.Strong knowledge of ANVISA regulations and other health authority requirements.Ability to work effectively without direct supervision and to be able to report succinctly and efficientlySkills
Excellent communication skills in Spanish, and English .Computer skills : very good knowledge of MS Office toolsProject management capabilities, including but not limited to creation of timelines, organization of meetings, meeting minutes, planning and executionSolution oriented working skillsTeamwork spirit, also able to perform aloneAnalytical thinking, problem solving capacityWell organizedExciting Challenges
Every day brings new opportunities to learn and grow.
Supportive Environment
We foster a culture of collaboration, where your ideas are valued, and your voice is heard.
Career Development
We're committed to helping you reach your full potential through ongoing training and development opportunities.
Recognizing Excellence
We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements.
Fun and Inclusive Culture
We believe in celebrating our successes and building strong connections within our team.
Ready to Ignite Your Passion?
If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you! Send us your resume today!
Please be informed that only selected candidates will be contacted.
Job Details
Seniority level : Mid-Senior levelEmployment type : Full-timeJob function : ScienceIndustries : Pharmaceutical ManufacturingWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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