Regulatory Affairs Manager
Technogarden AB / Biomedicinjobb / Malmö
2024-10-17
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hela Sverige Technogarden is cooperating with theBioInvent team that covers all aspects of drug development, including discovery, preclinical and translational research, manufacturing, and clinical development. On behalf of BioInvent, we are now looking for a
Regulatory Affairs Manager
As Regulatory Affairs Manager at BioInvent, you will plan, author and manage the assembly and timely submission of regulatory documentation for EU, US and RoW. The role will provide strong support and guidance to cross-functional teams (across multiple projects) and CROs.
The main responsibilities are as follows:
Regulatory Affairs Manager at BioInvent is responsible for operational regulatory work executing global regulatory strategies aimed at identifying and implementing the most efficient regulatory pathways for BioInvent's current and future drug development programs.
The responsibilities of the position include, but are not limited to:
Responsible for coordination, development, authoring and reviews of high-quality regulatory documentation for various types of regulatory submissions (e.g., core documents for IND/CTA, incl. substantial amendments/modifications, scientific advice packages, orphan drug designation applications etc.)
Coordinate preparation of responses to Health Authority requests for information
Work with internal cross-functional project teams and CROs to ensure timely deliverables to regulatory strategies for any company project goals
Oversight of CROs regarding CTR increased notification requirements and documentation redaction
Ensure maintenance of regulatory compliance, conformance of internal quality procedures and provide training to internal stakeholders with guidance on impact of new regulatory and scientific regulations
Support quality, regulatory, clinical and other personnel in the company as required regarding current regulatory policies and procedures.
Take on specific tasks as a representative of the Regulatory team, in line with your individual capabilities and interests.
Performing all duties in keeping with BioInvent's core values, policies, and all applicable regulations.
Requirements
At least 5 years experience in regulatory affairs in the biotech or pharmaceutical industry, with broad cross-functional regulatory knowledge in addition to special competence/interest within clinical regulatory documentation.
Working knowledge of Regulatory legislation, worldwide, and standard documentation/ document types including understanding of GDP.
Highly organized, proactive, and detail oriented
Experienced communicator and facilitator
Enjoy creating and participating in an efficient cross functional working environment
Effective time manager
Good organization and problem-solving skills
Proficient in MS Word, Excel, Power Point, Outlook
Good technical writing and editing skills
Proficient in written and spoken English
Qualifications
Educated to MSc level in a relevant science discipline.
Regulatory affairs experience including assisting in the developing regulatory submission documents and coordinating delivery to submission plans, usually demonstrated by 5+ year exposure
Reporting to: Senior VP Regulatory Affairs
Personal Profile
We are looking for a driven, structured, self-motivated and responsible person, who easily collaborates and communicates with others both verbally and in writing. You have excellent problem solving, and negotiation skills and you enjoy creating efficient working methods and contributing with your experience to ensure continuous improvements.
Personal suitability is of great importance, and we believe that you are efficient, have a strong commitment and ability to make things happen. You understand the importance of achieving results, keeping deadlines and to secure high quality within your work. You are enthusiastic and enjoy creating results and achieving goals both individually and together with your teams.
You will be part of a very exciting company and a great team with extensive and broad competence within biotechnology and regulatory affairs.
Location
Lund, Scania.
We are eager to talk to you and tell you more about the position and possibilities at BioInvent!
Ersättning Lön enligt överenskommelse
Så ansöker du Sista dag att ansöka är 2025-04-05
Klicka på denna länk för att göra din ansökan Omfattning Detta är ett heltidsjobb.
Arbetsgivare Technogarden AB (org.nr 556276-5189)
Arbetsplats Technogarden
Kontakt Carolina Pankarz Bernro
carolina.pankarz.bernro@technogarden.se 0730-981310 Jobbnummer 8961813