Beschreibung
* Prestigious, global player in biotechnology
* Temporary contract with extension option
## About Our Client ##
Our client is a small-sized company operating within the LIFE SCIENCE sector. They focus on delivering innovative solutions and maintaining high standards in their field. Known for their collaborative environment, they are dedicated to achieving excellence in their operations. It is a temporary contract with start asap (ideally November), till end of May 2025, with extension option. Hybrid work model.
## Job Description ##
The RA will be responsible for timely planning, preparation and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics. Tasks will include but are not limited to:
* Assist in the preparation and submission of regulatory documentation including Clinical Trial Applications (CTAs) and Marketing Authorisation Applications (MAAs) to ensure compliance with applicable guidelines.
* Support the coordination and tracking of regulatory projects and timelines.
* Maintain accurate records and databases for regulatory filings and correspondence.
* Collaborate with internal teams to gather necessary data and documents for submissions.
* Monitor and interpret regulatory requirements to ensure up-to-date compliance.
* Provide administrative support for regulatory meetings and audits.
* Contribute to the continuous improvement of regulatory processes and procedures.
* Stay informed about industry trends and regulatory changes affecting the LIFE SCIENCE sector.
## The Successful Applicant ##
A successful candidate should bring:
* A degree or educational background in a relevant field such as life sciences or regulatory affairs.
* 3-5 years\` experience in a Regulatory capacity, regulatory experience with CTAs and MAAs in Switzerland **is a Must-Have.**
* Proficiency in English; additional language skills are an advantage.
* Strong organizational skills and attention to detail.
* Familiarity with regulatory guidelines and processes in the LIFE SCIENCE sector.
* Ability to work independently and manage multiple tasks effectively.
* Experience with documentation management and regulatory tools is beneficial.
## What's on Offer ##
Our client offers you:
* An opportunity to work within a reputable company in the LIFE SCIENCE sector.
* A collaborative and supportive team environment in BASEL.
* Exposure to diverse regulatory projects and processes.
* The chance to contribute to meaningful work in a growing industry.
If you are ready to make an impact as an ASSOCIATE REGULATORY AFFAIRS in BASEL, we encourage you to apply today!
Quote job ref
JN-102025-6854295
Job Function
Healthcare & Life Sciences
Specialisation
Regulatory Affairs
Industry
Healthcare / Pharmaceutical
Location
Basel-City
Contract Type
Interim
Job Reference
JN-102025-6854295