QA Specialist

Gi Life Sciences Zürich recrute un(e) QA Specialist a Baar. Our client, headquartered in Baar, develops advanced diagnostics and therapies to improve patient outcomes. To support their growing team, we are looking for a versatile and motivated QA Specialist and Deputy RP (FvP/QP) to help shape a new and dynamic laboratory environment focused on
quality control of generics and nutritional supplements. In this role, you will play a key part in ensuring regulatory compliance and product quality across several Swiss legal entities. If you're passionate about software quality, regulatory compliance, and delivering impactful solutions in the life sciences industry, this could be the ideal opportunity for you. Quality Assurance Specialist (80%)
Your tasks

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Acting as Deputy QP (FvP), including batch disposition, recalls, and ensuring GDP-compliant distribution

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Leading and maintaining the local Quality Management System (QMS) in line with GMP/GDP standards

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Monitoring Out-of-Specification results, deviations, complaints etc. •
Management and scheduling of training

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Conducting management reviews, support with self-inspections, and review of



QUALIFICATIONS


and validation activities on behalf of the RP

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Reviewing analytical methods, specifications, method transfers, method validation, etc. on behalf of the RP

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Assisting and supporting the laboratory team in handling deviations, OOS-results, external complaints and investigations

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Assisting in the laboratory team in setting, changing and approval of product specifications

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Support the Responsible Person with the organization of customer audits and inspections by the authorities
Your



QUALIFICATIONS



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BSc or MSc in Pharmacy, Chemistry, Biotechnology, or a related field

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Knowledge of Swiss Therapeutic Product Acts and GMP/GDP guidelines

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Several years of experience in GMP/GDP and initial experience in quality assurance within a chemical / pharmaceutical environment

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Validation expertise particularly in the field of equipment



QUALIFICATIONS


, CSV and validation of analytical methods

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Structured and independent personality with a precise and reliable way of working

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Strong analytical mindset with the ability to manage risks, resolve issues, and drive continuous improvement

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Culturally sensitive, enjoy working in international teams and ability to work collaboratively in cross-functional teams

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Excellent communication skills, both written and verbal in English and German
Your application
Please apply online. For further information about the position, please contact your Gi Consultant, Ms. Marta Castellano
, MSc Biology (+41 76 342 57 90). Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton, BauTech and former Kelly Services. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 35 locations across Switzerland and over 250 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°. Gi Group SA Switzerland
Marta Castellano

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Profil recherché

and validation activities on behalf of the RP

• €¢
  
Reviewing analytical methods, specifications, method transfers, method validation, etc. on behalf of the RP

• €¢
  
Assisting and supporting the laboratory team in handling deviations, OOS-results, external complaints and investigations

• €¢
  
Assisting in the laboratory team in setting, changing and approval of product specifications

• €¢
  

Support the Responsible Person with the organization of customer audits and inspections by the authorities
Your