Junior Quality Associate (m/w/d) for CSL Behring

We make it GmbH; Bern; On-site; CHF 65,000 - 90,000; Full time

Job summary

CSL Behring AG in Bern is seeking a Junior Quality Associate to review PRO/QA and batch documentation, while spending significant time on the production floor to supervise aseptic processes. The role includes administrative support to the QA team and requires GMP experience, ideally in quality assurance, with strong IT skills.

Candidates without a scientific degree must have at least 5 years of GMP experience.

Qualifications

• GMP experience, preferably in Quality Assurance
• If no scientific degree, at least 5 years of GMP experience
• Strong proficiency in Excel, Word, OneNote, and other IT systems
• Experience using AI tools

Responsibilities

• Review of PRO/QA documentation
• Review of Batch Documentation
• High amount of time on the floor with production employees checking aseptic processes
• Administrative support of the team

Skills

GMP experience

QA experience

Tools

Excel

Word

OneNote

IT systems

AI tools

Job description

We make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion.

For our customer, the company CSL Behring, we are searching for:

Junior Quality Associate (m/w/d)

Description

CSL Behring AG in Bern specializes in the manufacture of drugs for the treatment of immune deficiencies and immune dysfunction, as well as drugs for rhesus prophylaxis and albumin solutions for shock and burn victims. CSL Behring AG's production facilities are licensed by the Swiss health authorities and the US FDA. Every year, therapeutically important proteins are isolated from over six million liters of human plasma in accordance with the strictest safety and quality standards and processed into medicines. The products of CSL Behring AG are distributed worldwide.

Working hours

Standard / 41 working hours

Availability for early morning shifts (starting at 05:00) and/or late evening shifts (after 22:00)

Tasks

• Review of PRO/QA documentation
• Review of Batch Documentation
• High amount of time on the floor with production employees checking aseptic processes
• administrative support of the team

qualifications

• GMP experience, preferably in Quality Assurance
• If no scientific degree (Bachelor's or Master's), at least 5 years of GMP experience required
• Strong proficiency in Excel, Word, OneNote, and other IT systems
• Experience using AI tools

We look forward to hearing from you.