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PM Group is a leading International engineering, architecture, project and construction management firm. With a network of offices in Europe, Asia and the US, we deliver complex, capital projects in the life sciences, food and beverages, mission critical/ICT, advanced manufacturing, energy and environmental sectors.
Who Are We
PM Group is an employee owned, international project delivery firm. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners.
Quality Engineering within the broader QA/RA function plays a key role in ensuring GMP compliance across production, analytical, and infrastructure systems, while supporting the continued growth and innovation of PM Group’s Life Sciences portfolio. To reinforce our high-performing team, we are currently seeking a motivated and technically strong QA Engineering Specialist (m/f/d).
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As a member of the QA Engineering team, you will play a central role in the lifecycle management of our GMP-relevant facilities and systems:
Ensure GMP-compliant operation of facilities throughout their entire lifecycle, including requalification, maintenance, change control, and deviation management
Contribute to qualification and validation projects (equipment, infrastructure, processes) and provide QA expert evaluation
Create, review, and approve GMP-relevant documents (e.g., URS, qualification packages, SOPs, logbooks)
Actively report and provide expert advice to stakeholders on technical and quality-related issues
Support regulatory authority inspections and customer audits, and coordinate time-critical activities such as PQR creation or batch document review
Lead smaller projects within QE and contribute to the further development of cross-functional quality processes
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Qualifications:
You work precisely, proactively, and responsibly – and you have the skills to succeed in a demanding GMP environment:
Completed bachelor's degree (BSc in Chemistry, Pharmacy, Process Engineering, or comparable field) or equivalent qualification with several years of QA experience
At least 5 years of professional experience in a GMP-regulated environment, ideally in qualification/validation or technical QA processes
Solid GMP knowledge of Switzerland and EU, and confident creation and evaluation of GMP-relevant documents
Proficient use of MS Office, ERP/MES/QM systems, and digital communication and planning tools
Analytical and structured working style, high solution orientation, strong communication skills, and professional collaboration with internal and external stakeholder's
Fluent German skills
Why PM Group?
As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2029 business strategy. Click here to read more in our Corporate Responsibility and Heath, Safety & Well-being Report.
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
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