Consultant Regulatory Affairs Pharma Regulatory Affairs • • Hybrid Remote

TRIUM Clinical Consulting NV; Granada; A distancia; EUR 30.000 - 60.000; Jornada completa

Descripción de la vacante

Join a forward-thinking company as a Consultant in Regulatory Affairs, where you will provide essential regulatory writing services and support senior team members. This role emphasizes clinical documentation and requires a strong understanding of European and UK regulations. You will thrive in an international environment, building connections while ensuring high-quality project delivery. With a commitment to continuous learning and a supportive community, this position offers a unique opportunity to grow within the life sciences sector. Be part of an award-winning team that values your contributions and celebrates achievements together.

Servicios

Attractive salary package

Career development opportunities

Job security

Supportive work environment

Formación

• University degree in life sciences or chemistry required.
• General knowledge of European/UK pharmaceutical regulations is essential.

Responsabilidades

• Provide regulatory writing services with emphasis on clinical documents.
• Monitor changes in guidance/legislation and inform the team.

Conocimientos

Regulatory Writing

Attention to Detail

Communication Skills

Organizational Skills

Analytical Mindset

Educación

University Degree in Life Sciences

University Degree in Chemistry

Descripción del empleo

QbD Group offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, Biotech and Medical Devices / IVD.

Our Regulatory Affairs division supports customers throughout the entire regulatory lifecycle of their products, whether they are traditional pharmaceutical products, generic medicines, vaccines, biologicals, biosimilars, medical devices, IVDs or Advanced Therapy Medicinal Products (ATMP). Our RA division has a strong international presence with over 30 colleagues in Belgium, the Netherlands, the UK, Spain and Austria. Our customer portfolio spans the entire globe (Asia, US, Europe, Africa).

We are looking for a Consultant Regulatory Affairs Pharma to join our team.

What do we expect from you as a Consultant Regulatory Affairs Pharma?

1. You provide a range of regulatory writing services with supervision of senior team members with an emphasis on clinical documents (clinical trial applications, scientific briefing packages, orphan drug designations, paediatric investigation plans) with a focus on European and UK procedures.
2. You deliver projects on time and to a high quality.
3. You assist senior team members with their projects.
4. You provide QC functions within the QbD team (e.g., translations of product information compared to templates; clinical and nonclinical overviews compared to source data).
5. You develop and maintain regulatory skills and knowledge necessary to ensure effective support to clients.
6. You monitor changes in guidance / legislation in designated areas and inform the team.
7. You build a network of industry colleagues and professional associations.
8. You complete basic job-related responsibilities e.g., maintenance of personal training records, timesheets, project archiving.

Who are we looking for?

• You have a university degree in life sciences or chemistry.
• You have a general knowledge of European / UK pharmaceutical regulations and guidelines.
• You have some relevant regulatory affairs experience.
• You have attention to detail.
• You have good written and verbal communication skills.
• You possess good organizational skills and an analytical mindset.
• You enjoy working in an international environment.

A true QbD’er can be recognized by the following qualities :

• Resilient: Your strong and positive attitude helps you overcome any challenge.
• Hungry for knowledge: You are always open to learning.
• No non-sense mentality: You can be straightforward in a respectful way.
• Innovative: You are constantly looking for new and better solutions.
• Not too serious: Your job is serious, but you don’t take yourself too seriously.

What’s in it for you?

• QbD Group offers you an attractive and competitive salary package, tailored to individual needs, considering legal requirements and local laws and regulations.
• Join us to build a sustainable career, where job security is ensured, and lasting, meaningful connections are formed.
• As we’re a knowledge-based company, you’re guaranteed to embark on a continuous journey of learning and development.
• Be part of our global success story. As an award-winning company, we value everyone’s contribution and celebrate achievements together.

Our promise to you :

• As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
• Moreover, we aim to create a joyful community where you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals.
• In short … We stand for JPEG: J oy in P artnership, going for the E xtra mile to G et things done!

Interested? Send us your CV and motivation letter, and who knows, we might welcome you soon into our QbD family!