Regulatory Affairs Manager (a)

• 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 (latest November), till end of May 2025, with a strong take-over option. Hybrid work model. Fully remote also possible but the person has to live in Switzerland.

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 (licensed products) 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 ideally with licensed/marketed products in the pharma industry, experience with Swiss Medic is a Must-Have.
• Proficiency in English (work language); Technical German (write & read) e.g for labelling reviews, is a Must-Have.
• Ability to work independently and manage multiple tasks effectively in a fast paced work environment.
• Experience with documentation management, archiving systems, and regulatory tools (e.g. Veeva RIM).

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