
Quality Manager - GMP & Project Management
1w1 week agoSiemens
AT · Full-time · €42,000 – €42,000
About this role
SIEMENS Personaldienstleistungen (SPDL), a subsidiary of Siemens AG Österreich with over 25 years of experience, offers challenging tasks within the Siemens group and renowned clients across Austria. The company values fair chances, cultural diversity, and shared successes. It seeks a Quality Manager for long-term full-time assignment (38.5 hours/week) to one of the world's largest pharma companies.
In this role, you take responsibility for complex cross-site projects ensuring cGMP compliance and manage quality initiatives across the project lifecycle. You ensure adherence to internal and external quality and regulatory requirements, including SOPs and authority demands. Provide expert support to project and line functions on GMP-relevant issues while conducting independent due diligence.
Work in a dynamic environment supporting global stakeholders in pharmaceutical quality and operations. Collaborate with diverse teams emphasizing compliance and risk assessment in technical development and production. Engage with an international network fostering professional growth.
Benefit from a minimum gross monthly salary of EUR 3,500, exceeding the collective agreement minimum, with final agreement based on qualifications and experience. As part of an international corporation, enjoy career perspectives and training options to fully utilize your potential. Submit your online application to join this challenging position.
Requirements
- Completed natural sciences degree with extensive experience in pharmaceutical quality, production, or operations
- Proven cGMP expertise and experience in Technical Development, QA, and/or Production
- Ability to analyze, evaluate, and decide on complex cGMP and compliance issues
- Experience in complex cross-site projects and interaction with global stakeholders
- Fluent business English with strong organizational, communication, and assertiveness skills
Responsibilities
- Take responsibility for complex, cross-site projects ensuring cGMP compliance
- Ensure compliance with internal and external quality and regulatory requirements (cGMP, SOPs, authorities)
- Drive and implement quality initiatives across the entire project lifecycle
- Provide expert support to project and line functions on quality and GMP issues
- Conduct independent due diligence activities and assess quality and compliance risks
Benefits
- Minimum gross monthly salary of EUR 3,500 (exceeds collective agreement minimum)
- Career perspectives in an international corporation
- Training and development options to utilize full potential
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