R

Rentschler Biopharma

CDMO delivering biopharmaceutical development and manufacturing

Sachbearbeiter - QA-Systeme

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLaupheim, Germany

About the Job

Requirements

  • Completed commercial or operational vocational training, or a comparable qualification.
  • IT affinity and willingness to learn new IT systems.
  • Team-oriented, open, and trustworthy collaboration.
  • Independent and structured working style, with interdisciplinary thinking.
  • Very good communication skills to convey user knowledge clearly.
  • Business-fluent German and good English skills.

Responsibilities

  • Maintain the relevant modules in MasterControl on schedule.
  • Assign and adjust user roles in MasterControl according to established requirements.
  • Maintain and approve departmental and cross-functional training profiles.
  • Represent the QA training coordinator function.
  • Create departmental training materials using Articulate Rise 360 in SCORM format.
  • Support organization of the annual mandatory GMP training.
  • Create and edit module-specific reports.
  • Contribute to optimizing and developing the user and training management module and identifying improvement opportunities.
  • Work closely with internal departments and functions involved in user and training management.
  • Take turns providing support for the MasterControl hotline as part of the team.
  • Assist users with technical questions and access problems.
  • Adjust workflows when covering for colleagues.
  • Maintain the data structure.

Desired Qualifications

  • Knowledge of the GMP-regulated pharmaceutical industry environment is desirable.

About the Company

Rentschler Biopharma

CDMO delivering biopharmaceutical development and manufacturing

What the company does: Rentschler Biopharma provides contract development and manufacturing services for biopharmaceuticals, helping other pharmaceutical companies develop and produce complex medicines. How its products work: It offers end-to-end services in biopharma development and manufacturing, backed by facilities and staff that design, optimize, and produce biologic drugs at scale for clients, including a major site in Milford, MA that has expanded capacity to serve the international market. How it differs from competitors: It has a long heritage in biopharma, a dedicated CDMO focus since 1997, and a global footprint with a major U.S. site and expanded capacity, positioning itself as a reliable partner for developing and manufacturing complex biologics. What its goal is: To be a trusted partner for pharmaceutical companies by providing development and manufacturing services at scale, supporting clients as they bring biologic medicines to market.

Company size
501-1,000
Company stage
Series A
Total funding
$1.6M
Headquarters
Laupheim, Germany
Founded
1927

Recently Posted Jobs

Explore more opportunities at Rentschler Biopharma

See more jobs