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p>For our client, a pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist.
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p>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.
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General Information:
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Start Date: ASAPDuration: 6 months contractExtension: unlikely (maternity cover)Workload: 100%Workplace: Schachen, LuzernHome office: possible in exceptional cases upon discussion, but role mainly on-site based
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p>Responsibilities include but are not limited to:
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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 workProvide support to projects and source areas as Quality Assurance Representative
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p>Your profile:
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BA/BS or higher academic educationAt least 2 years of experience in a regulated industry (GMP), preferably in pharmaceuticals, biotechnology, or medical technologyProficient IT acumenExperience in conducting quality oversight activitiesFocus on quality and complianceService- & customer-oriented mindsetAbility to set priorities and meet deadlinesStrong problem-solving skillsExcellent communication skills and fluency in EnglishUnderstanding of German language (intermediate+ level)Project Management experience (nice to have)6sigma green-belt certifications (nice to have)