Quality Manager

ref: 23175


SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

The company

Our client is a professional Pharmaceutical organization, based in Luzern Switzerland.
Our client is a Pharmaceutical company in Switzerland

Role description

In this role you will be responsible person for Switzerland and deal with the Swiss Health Authorities

Responsibilities

Release commercial products independent from commercial functions
Processing complaints defects in quality
Processing quality defects, deciding on or possibly initiating measures necessary
Taking decisions concerning destruction of returns Forwarding requests for exceptional re-use of returns
Planning and monitoring of general GDP training of employees (initial training, GxP-awareness training).
Quality oversight / auditing for external service providers (e.g. external warehouse).
Contact person for Quality/Technical Agreements defining GXP responsibilities Decision making for all Quality issues.
Maintenance of metrics and support the quality
Regional Inspectorate, and the Cantonal Health Authority Meeting regularly with Swiss Logistic and Regulatory to assure alignment of activities
Close cooperation with Pharmacovigilance Country
Lead Participating in regular meetings with EMEA Regional Quality Operations

Requirements

Life Science Degree(e.g. Masters degree) in pharmacy, medicine, biology or a comparable discipline
Qualified or Responsible Person, preferably in Switzerland.
Eligible to be a Deputy Qualified Responsible Person in Switzerland 3 to 5 years of experience in Quality Assurance (GMP/GDP)
Fluency in German and English, preferably also French

Secondary benefits

  • Pension Plan
Country
Switzerland
Region
Luzern
Sector
Pharmaceuticals
Specialization
Quality, Regulatory Affairs, Continuous Improvement
Employment type
Freelance
Experience
3-5 Years
Education
Master
Location type
On location
Salary
Negotiable - Negotiable
Language
English, German