QA Specialist/QMS associate; m/w/d
Listed on 2026-09-30
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Quality Engineering
Shape the Future of Pharmaceutical Quality with Techfirm Engineering
Techfirm Engineering is looking for a QA Specialist / QMS associate (m/w/d) to join our Industrial Services team in Switzerland.
The selected consultant will take over activities from a QA professional leaving the organization 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, Deviations - Act as a Quality Approver for relevant documentation.
- Support QMS-related activities and quality processes.
- Prepare and maintain quality reports and documentation.
- Support audit activities and provide the necessary documentation and follow-up.
- Support the vendor onboarding process, ensuring that quality and GMP requirements are appropriately addressed.
- Participate in and support governance meetings.
- Collaborate with internal stakeholders and cross-functional teams to ensure compliance with applicable GMP requirements.
Experience:
- A first previous experience in a GMP-regulated pharmaceutical environment.
- At least 1 year of experience within Quality Assurance / Quality Management Systems (QMS).
- Experience with GMP documentation review and approval.
Strong attention to detail and quality mindset.
Structured and organized approach.
Autonomous and proactive working style.
Good communication and stakeholder management skills.
Ability to work effectively in a regulated and collaborative pharmaceutical environment.
Fluent English required.
German is an advantage.
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.
PLEASE NOTE:
only candidates with valid Swiss/EU/EFTA work authorization can be considered.
- Work location 4001 Basel (BS)
- Workload 100%
- Employment start Immediately
- Employment duration Permanent
- Qualification skilled
- Work experience More than 1 year
- Education Master’s degree from a university of applied sciences or equivalent
- English Orally :
Very good knowledge Written :
Good knowledge
- By email m.georgler
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