QA Specialist / QA Specialistess

Shape the Future of Pharmaceutical Quality with Techfirm Engineering

Techfirm Engineering is seeking a QA Specialist / QMS Associate (m/w/d) to join our Industrial Services team in Switzerland. The selected consultant will take over responsibilities from a departing QA professional and will support the Quality function with a strong focus on GMP documentation review, quality approval, QMS activities, and audit support.

Responsibilities

• Review and approve quality and GMP documentation.
• Review and manage logbooks, GMP documents, GMP procedures, and deviations.
• Act as a Quality Approver for relevant documentation.
• Support QMS-related activities and quality processes.
• Prepare and maintain quality reports and documentation.
• Assist in audit activities by providing necessary documentation and follow-up.
• Support the vendor onboarding process, ensuring that quality and GMP requirements are adequately addressed.
• Participate in and support governance meetings.
• Collaborate with internal stakeholders and cross-functional teams to ensure compliance with applicable GMP requirements.

What We Are Looking For

Experience

• A minimum of one year of experience in a GMP-regulated pharmaceutical environment.
• At least one year of experience within Quality Assurance / Quality Management Systems (QMS).
• Experience with GMP documentation review and approval.

Personal Skills

• Strong attention to detail and a quality mindset.
• Structured and organized approach.
• Autonomous and proactive working style.
• Excellent communication and stakeholder management skills.
• Ability to work effectively in a regulated and collaborative pharmaceutical environment.

Languages

• Fluent English is required.
• German is an advantage.

Why Techfirm?

At Techfirm Engineering, you will:

• Join a Swiss-headquartered company with a multicultural and collaborative environment.
• Work on meaningful pharmaceutical and quality projects in Switzerland.
• Contribute to GMP-compliant quality activities within a leading life sciences environment.
• Collaborate with experienced quality and pharmaceutical professionals.
• Develop your expertise through challenging and meaningful assignments.
• Be part of a company culture focused on respect, professional growth, and employee well-being.

Ready to Join Us?

If you have experience in QA, QMS, and GMP documentation and are eager to take the next step in your career, we encourage you to apply online using the form below. Please note that only applications matching the job profile will be considered.

Please note: only candidates with valid Swiss/EU/EFTA work authorization can be considered.