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QC Consultant

Strandassociates

Niort

À distance

EUR 40 000 - 55 000

Plein temps

Il y a 7 jours
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Résumé du poste

Join a leading company in quality control and regulatory affairs, where you will manage projects for clients in the pharmaceutical and biotech sectors. You will contribute to method validation, product management, and continuous improvement initiatives while enjoying a competitive salary and benefits. The role offers an optimal work-life balance with flexible hours and remote work options, alongside opportunities for professional development and social engagement within a community of experts.

Prestations

Competitive salary
12 additional leave days
Flexible hours
Remote work options
Training and workshops

Qualifications

  • Initial experience in R&D or quality control.
  • Experience in the life sciences industry.
  • Knowledge of GMPs.

Responsabilités

  • Writing protocols and reports.
  • Method validation and transfer.
  • Participating in continuous improvement projects.

Connaissances

Communication

Formation

Degree in Sciences

Description du poste

Join a community of over 80 experts in your field

Depending on your level of experience, you will contribute to or lead the management of projects or operational services related to quality control for various clients (pharmaceutical, biotech, medtech), such as:

  1. Writing protocols and reports;
  2. Method validation;
  3. Method transfer;
  4. Product management;
  5. Continuous improvement projects; proposing plans for continuous improvement to create value or demonstrate proactivity within your assignment;
  6. Participating in tailored training to develop your soft and hard skills;
  7. Attending or organizing workshops/events for knowledge sharing with colleagues;
  8. Monitoring your projects and personal development with your dedicated Talent Manager and Business Manager.

Minimum requirements include:

  • A degree in sciences (preferably);
  • Initial experience in R&D or quality control;
  • Experience in the life sciences industry;
  • Knowledge of GMPs;
  • Excellent communication skills (spoken and written);

We offer:

  • An attractive salary aligned with market standards and your experience;
  • A salary package with highly competitive fringe benefits;
  • Optimal work-life balance with 12 additional leave days, flexible hours, and remote work options;
  • Join a community of over 80 consultants in quality and regulatory affairs, with many social events organized throughout the year;
  • Training and workshops to develop and share your skills.
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