Quality Specialist GMP (m/f/d) 100%

Quality Specialist GMP (m/f/d)

Your next career move in pharmaceutical quality awaits you

Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a GMP-regulated environment where precision and compliance meet innovation? Join a dynamic team and make a real impact in bringing life-changing therapies to patients worldwide.

• Duration: 01.01.2026 to 30.06.2026 (extension possible based on fincancial approval)
• Location: Basel
• Type: Temporary position
• Remote Working: No
• Pay Rate: CHF 34/h to CHF 43/h

About our client

For our client, a globally recognized pharmaceutical company specializing in cutting-edge oncology and ophthalmology treatments, we are seeking a dedicated Quality Specialist (m/f/d). This innovative organization is at the forefront of developing novel therapies and maintains the highest cGMP standards in their state-of-the-art facilities in Basel. With a strong commitment to quality excellence and patient safety, they offer a collaborative environment where your expertise will directly contribute to advancing healthcare.

Your responsibilities

• Review and release GMP documentation including batch records, packaging documents, and investigational medical product files to ensure regulatory compliance
• Facilitate timely batch release of labels, primary packaging materials, and clinical trial supplies according to strict quality standards
• Provide functional expertise to cross-functional teams and support quality assurance activities across the technical research and development unit
• Manage document workflows by receiving, scanning, filing, and archiving quality-critical documentation such as Certificates of Compliance and review checklists
• Contribute to quality improvement projects including tool development, process optimization, quality risk assessments, and validation activities
• Ensure cGMP adherence by applying internal SOPs, regulatory guidelines, and health authority requirements in all quality-related tasks
• Support qualification activities for facility upgrades, IT validation projects, and implementation of quality management systems

Your profile

• Technical or scientific education with a Bachelor's degree and minimum 3 years of pharmaceutical/biotech experience, or Technician diploma with at least 5 years of relevant experience
• Solid cGMP knowledge and understanding of regulatory requirements in pharmaceutical quality assurance and batch release processes
• Experience in GMP documentation review, batch record evaluation, or quality control in a regulated pharmaceutical environment
• Strong communication skills to effectively collaborate with production, quality control, and cross-functional teams on compliance matters
• Fluent English (written and spoken) is essential; proficiency in German is advantageous
• Organizational excellence with the ability to manage multiple priorities and meet critical deadlines in a fast-paced environment
• Basic understanding of drug development processes and investigational medicinal product manufacturing
• Completed GMP training or willingness to undergo comprehensive training before task assignment

What nemensis offers you

• Nemensis AG is your specialized personnel consultant in the Life Sciences sector with headquarters in Basel
• Comprehensive consultation and support throughout the entire application process by our experienced consultants
• Access to an extensive client network and exciting opportunities in Northwestern Switzerland
• Fast and uncomplicated entry through individual guidance and professional advice during the application process

Ready to elevate your quality career?

At nemensis ag, we've connected thousands of professionals with their dream jobs, giving them the opportunity to develop further or re-enter the job market. What can we do for you and your career today? Get in touch with us!

We're looking forward to hearing from you for the position as Quality Specialist GMP (m/f/d) in Basel. Apply now and become part of a team that sets the standard in pharmaceutical quality!

? Phill Rogers, Consultant, Write an email

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