Regulatory Affairs Officer Cmc - Biological Products Specialist [Uo515]

buscojobs España; Madrid; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a Regulatory Affairs Officer for their CMC unit. The role involves managing product-specific dossiers, supporting drug development, and ensuring quality and customer satisfaction. Ideal candidates should have a background in Health Sciences and experience in CMC. Join a dynamic team and enjoy a hybrid work model with opportunities for personal development.

Servicios

Permanent contract

Hybrid Model

Training and personal development program

Well-being programme

Internal activities & RSC Activities

Formación

• 2 years’ experience in CMC in Regulatory Affairs.
• Specializing in biological products.

Responsabilidades

• Global CMC drafting and management of product specific dossiers.
• Support in responses to deficiency letters and CMC support during drug development.
• Establishment and improvement of CMC related processes.

Conocimientos

Analytical Skills

Quality-oriented

Customer-focused

Communication Skills

Team Player

Educación

Health Sciences

Biochemistry

Biotechnology

Biomedicine

Descripción del empleo

Asphalion is growing and we are looking for a Regulatory Affairs Officer to join our CMC unit of consultants for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an international environment and who wants to grow with us!

Main responsibilities :

• Reporting to : CMC Manager
• Global CMC drafting / management of product specific dossiers (Mod. 2 / Mod. 3), with special focus on biological products, including new registration applications, variation packages and renewal packages in EU, US and RoW markets.
• Support in responses to deficiency letters, including coordination and preparation of responses to questions.
• CMC support during drug development, including writing CMC sections of IMPDs and INDs.
• RA CMC change control evaluation / management, when necessary.
• RA CMC liaison with clinical and non-clinical teams, RA lifecycle management teams, technical / subject matter experts, QA, QC, production and supply, as per project needs.
• Successful client management of regulatory affairs.
• Establishment and improvement of CMC related processes and work instructions.
• Responsible for meeting deadlines, ensuring quality first time and maintaining customer satisfaction.
• Preparation and participation as a speaker in internal and external team related training sessions focused on CMC of biologics.

Requirements :

• 2 years’ experience in CMC in Regulatory Affairs in the Pharmaceutical Industry and / or Consultancy is required.
• Specializing in biological products.
• Background in Health Sciences, preferably biochemistry, biotechnology, biomedicine and related careers.
• Good analytical, quality-oriented, and customer-focused skills.
• High level of English and Spanish.
• Willing to learn and take on new challenges and responsibilities.
• Good team player with good communication skills.
• Ability to handle multiple tasks / projects in a fast-paced environment.
• Truckloads of motivation, positivity, and enthusiasm.

Why working at Asphalion?

• Permanent contract.
• Hybrid Model (You can work everywhere in Spain).
• Wide variety of projects, new challenges and experiences.
• Training and personal development program.
• A professional, inclusive and high-performance work environment to develop your skills and grow your career. A great company culture built around Passion, Flexibility, Commitment, Quality & Companionship.
• A highly & dynamic working environment with employees from more than 15 nationalities.
• Our people and their well-being are our priority : Physical, psychological and emotional well-being programme.
• Internal activities & RSC Activities.
• Equal Opportunity Employer.

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