Quality Assurance Specialist.

For our client, a pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist.
 

In this role you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.

General Information:
 

• Start Date: ASAP
• Duration: 6 months contract
• Extension: unlikely (maternity cover)
• Workload: 100%
• Workplace: Schachen, Luzern
• Home office: possible in exceptional cases upon discussion, but role mainly on-site based

Responsibilities include but are not limited to:
 

• Conduct quality review and approval of GMP documentation (e.g. calibration activity documentation, equipment periodic review, logbooks, training plans and records, SOPs)
• Support quality oversight activities under the responsibility of the Quality Operations and Compliance area (e.g. calibration, equipment periodic review, logbooks, management for training plans and training records, SOPs, quality on the floor)
• Assure and maintain compliance with GMP regulations in the defined scope of work
• Provide support to projects and source areas as Quality Assurance Representative 

Your profile:
 

• BA/BS or higher academic education
• At least 2 years of experience in a regulated industry (GMP), preferably in pharmaceuticals, biotechnology, or medical technology
• Proficient IT acumen
• Experience in conducting quality oversight activities
• Focus on quality and compliance
• Service- & customer-oriented mindset
• Ability to set priorities and meet deadlines
• Strong problem-solving skills
• Excellent communication skills and fluency in English
• Understanding of German language (intermediate+ level)
• Project Management experience (nice to have)
• 6sigma green-belt certifications (nice to have)