QC Molecular Biology Analyst

About the role:

Are you passionate about molecular biology and quality control in the pharmaceutical industry? Join us as a QC Molecular Biology Analyst and contribute to the development and manufacturing of innovative gene therapy products that transform lives.

In this role, you will ensure the accurate execution of molecular biology assays, maintain compliance with Good Manufacturing Practices (GMP), and help deliver high-quality products to patients worldwide.

Key Tasks:

• Execute the Molecular Biology assays corresponding to GMP and Toxo batch characterization, raw material testing as well as comparability studies and others.
  
  
• Perform assays for the development, qualification and validation of molecular biology analytical methods.
  
  
• Ensure the accurate and precise execution of testing procedures according to established procedures.
  
  
• Maintain detailed and organized records of all testing activities ensuring data integrity.
  
  
• Report to the QC Molecular Biology Lead any deviation or OOS/OOE/OOT detected.
  
  
• Assist in drafting protocols, reports, SOPs, and related documentation.
  
  
• Identify opportunities for improvement in analytical methodology and laboratory documentation, proposing updates to enhance consistency and regulatory compliance.
  
  
• Actively participate in lab maintenance, cleanliness and management and inventory control of critical reagents and stock.
  
  
• Collaborate with team members to resolve issues and improve QC processes.

Key Working Relation:

• Quality departments

• R&D department

Skills & Qualifications:

• Professional education in quality control and pharmaceutical products or similar, or University degree in Biochemistry, Molecular Biology, Biotechnology, or related field.
  
  
• Previous experience of 1 year in a QC role within the biopharmaceutical or biotech industry.
  
  
• Minimum 1 year in a QC role, preferably in pharmaceutical or biotech settings.
  
  
• Proficiency in molecular biology techniques (qPCR, dPCR, sequencing, gel electrophoresis).
  
  
• Level of English to be able to perform the activities of the department (B1).
  
  
• Knowledge of GMP or experience of working in a highly regulated industry.
  
  
• Organizational and planning skills: set goals and priorities when performing a task, agreeing on the action, deadlines, and resources to be used.
  
  
• Strategic and improvement vision: encourage a culture of innovation and learning by contributing ideas and continuous improvements.
  
  
• Achievement of results: direct all actions towards the expected goal.
  
  
• Excellent communication and interpersonal skills, with the ability to work collaboratively across teams.
  
  
• Ability to work in a fast-paced environment and manage multiple tasks effectively.
  
  
• Company values: Humility, Empathy, Responsibility, Commitment, Teamwork, and Effort.

We Offer:

A dynamic and collaborative work environment.
Opportunities for professional development and continuous training.
Direct impact on the development of therapies that improve people's lives.
Additional benefits; health insurance, flexibility, etc.

If you’re looking for a role where your work truly matters and you want to grow in a dynamic, forward-thinking company, apply today and help us shape the future of gene therapy!