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Le poste

Quality Assurance Intern

 

Become part of a team of 30 employees, united by strong values: excellence, shared vision, team spirit and respect. In a dynamic and multicultural environment, you will contribute to impactful projects while developing your skills. AUROBAC THERAPEUTICS offers a professional setting that fosters growth, engagement and continuous development. Let’s build the future together!

Presentation of the company:

AUROBAC THERAPEUTICS is a biopharmaceutical company created in 2022 by three renowned life sciences innovation companies, Boehringer Ingelheim, Evotec and bioMérieux, to become a global leader in the fight against bacterial infections, Antimicrobial Resistance (AMR) and their consequences in acute hospital settings.

With strong growth ahead, within an international environment, the company is now looking for a Quality Assurance Intern.

Description:

As a Quality Assurance Intern at AUROBAC THERAPEUTICS, you will integrate the Quality Assurance team and actively contribute to the management and improvement of the company’s Quality Management System (QMS). Your key responsibilities will include 1) Identifying and implementing solutions to optimize QMS documentation management; 2) Participating in internal audits and quality controls of R&D processes and documentation; and 3) Supporting the deployment of continuous improvement actions.

You will report to the Quality Assurance Coordinator and work closely with all AUROBAC THERAPEUTICS Teams.

Missions:

• Contribute to the Optimization and Improvement of QMS Documentation Management

✓ Analyze current practices related to QMS document management

✓ Benchmark and compare different tools that help streamline document management based on defined criteria (e.g., Document Management System (DMS), other collaborative digital platforms or software)

✓ Propose an implementation plan or roadmap for the chosen solution

✓ Contribute to the implementation of the chosen solution

• Participate in Internal Audits/Quality Controls (QCs) to drive R&D process Compliance and Continuous Improvement

✓ Support the Quality team in the preparation of internal audits and QCs by creating audit checklist and questionnaire

✓ Assist the Quality team in the conduct of audits and QCs with interviews of staff members and review of records

✓ Analyze the outcome of audits/QCs and identify improvement actions with concerned staff

✓ Participate in the preparation of audit/QC reports and follow-up of action plan (CAPA) with the relevant stakeholders

• Support with the implementation of Quality Actions aiming at promoting the Quality Culture and QMS maintenance and improvement

✓ Participate in the periodic review of QMS documentation

✓ Follow-up of QMS CAPA with relevant stakeholders

Personal and Technical Skills:

• Fluency in English is a must-have

• Excellent organizational and communication skills

• Rigorous, with analytical skills, paying attention to details, able to synthesize information

• Ability to solve problems proactively, and adaptability

• Ability to work both independently and cross-functionally (project mode)

Education:

• Student (Master’s level - BAC +5/6) in Pharmacy, Biotechnology or Engineering preferably with a specialization in Quality Management

Perks:

• Meal vouchers and on-site restaurant

• Public transport contribution

• Gym and collective classes access

• Concierge

To apply, please send your CV and cover letter application to jobs@aurobac-tx.com mentioning the reference ATX25-12

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Voir l'annonce sur le site de l'entreprise

 

 

L'entreprise

AUROBAC THERAPEUTICS

 

AUROBAC THERAPEUTICS is a biopharmaceutical company created in 2022 by 3 renowned life sciences innovation companies, Boehringer Ingelheim, Evotec and bioMérieux, to become a global leader in the fight against bacterial infections, Antimicrobial Resistance (AMR) and their consequences in acute hospital settings.
We focus our efforts to develop the next generation of antimicrobial and acute care products, following a targeted precision medicine approach, i.e. associated with rapid diagnostics to support product use.

 

Domaine d'application

  • Biotech - Pharma

Fonction

  • Affaires Réglementaire & Qualité

Contrat

  • Stage

Expérience

  • Aucune
  • De 1 à 2 ans

Niveau d'étude

  • BAC + 5 / Master

Localisation

  • 69 - Rhône

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