Technical Regulatory Cmc Writer F - M H/F Astek
- Belgique
- CDI
- Télétravail partiel
- Bac +2
- Secteur informatique • ESN
- Exp. 3 ans min.
Les missions du poste
Your mission (should you decide to accept it):
Your potential challenges will be various, depending on the clients' priorities. The list below gives you examples of our classic activities.
Your daily activities will be:
- The Technical Regulatory Writer is involved in the company's regulatory activities related to new & existing products, on a domestic or international basis. Activities focus on technical writing for Facilities, major and minor submissions....
- Write CMC, facility and equipment parts and new files for WW regulatory File.
- Manage and schedule with SMEs and Site conformance (and Production, Validation and Quality Assurance) the writing/review process to ensure timely completion.
- Ensure the coordination with the departments involved in the writing/review process.
- Write and support regulatory affairs Responses to Questions raised by Regulatory Authorities.
- Monitor that supportive data provided by other departments are compliant.
- Report significant issues.
- Manage the projects within all company/GRA tracking tools.
- Assess the change controls that relate to pure facilities and equipment matters or work with GRL teams for change controls impacting both CMC and facilities.
Le profil recherché
You:
- University level (Life Sciences background is preferred) or equivalent by experience.
- At least 3 years of experience in writing CMC (technical) parts of regulatory documents (registration files or variations).
- Experience working in validation/QA/production in Biologics/Pharmaceuticals industry.
- Knowledge of regulatory procedures / systems / guidance.
- Knowledge of biologic process and process equipment.
- Knowledge of Qualification / Validation principles.
- Manages own time to meet agreed short-term targets.
- Microsoft.
- PowerPoint & Excel.
Astek en images
Publiée le 12/06/2026 - Réf : 4885