Quality Assurance Specialist (m/f/d) – Clinical Supply | PTA / CTA / PKA in Rheinfelden

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Location/Division Specific Information

Fisher Clinical Services GmbH is a subsidiary of Thermo Fisher Scientific Inc. and is a market leader in Clinical Supply Chain Management Services and Clinical Supplies for patients worldwide. You can find out more about our location in Weil am Rhein and Rheinfelden here: www.fisherclinicalservices.com

Discover impactful Work

Are you a PTA, PKA, CTA or have a comparable vocational qualification and would like to develop your career in pharmaceutical Quality Assurance?

Join our Quality Assurance team in Rheinfelden and support our Qualified Persons (QPs) in the certification and release of clinical trial materials for patients worldwide.

A university degree is not required for this position.

A Day in the Life

In this role, you will ensure that all required quality documentation is complete, compliant and available for timely batch certification and release.

Your responsibilities include:

• Preparing and reviewing documentation for QP certification and batch release
• Coordinating and tracking quality documents with customers, project managers and internal teams
• Preparing Certificates of Release, Confirmations of Import and QP Declarations
• Verifying country-specific clinical trial approvals
• Maintaining QP tracking tools and compliant documentation records
• Supporting SOPs and other quality documents
• Supporting audits, inspections, investigations and CAPA activities
• Contributing to continuous improvement of our QA processes

Keys to Success

Education:

• Completed vocational training as PTA, PKA, CTA, Pharmaceutical Assistant or a comparable qualification
• No university degree required

Experience & Skills

• Experience in pharmaceutical Quality Assurance, Quality Control or another GMP-regulated environment is an advantage
• Good understanding of GMP/GDP requirements
• Structured and detail-oriented way of working
• Strong organizational and documentation skills
• Good communication and teamwork skills
• Fluent German and good English
• Good Microsoft Office skills; SharePoint, TrackWise or eDMS experience is beneficial

What we offer

• Employment with an innovative, future-oriented organization
• Outstanding career and development prospects
• Company pension scheme and other fringe benefits
• Exciting company culture which stands for integrity, intensity, involvement and innovation

We are EEO/Affirmative Action Employer

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of , color, religion, _ , orientation, gender identity, national origin, disability or any other legally protected status.

At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

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