Quality Assurance Manager Deputy QP
Location: SwitzerlandSIRE 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 Aargau Switzerland.
Our client is a Pharmaceutical company in Switzerland focused on finished products.
ROLE DESCRIPTION
Review, check and approve batch documentation and any associated deviations to ensure they are satisfactorily completed prior to batch certification by the QP
Support the shipment, quarantine and rejection procedures for materials received or manufactured at the site.
Support the QP in the execution of their legal and routine duties.
RESPONSIBILITIES
Liaise with external contractors and personnel regarding the release of finished product.
Prepare any required CAPA's related to the release of finished product.
Support for the artwork approval process.
Handle customer complaints, deviations, CAPA’s and change controls, assisting in root cause analysis, prompt responses/ resolution and ongoing data evaluation to ensure any emerging trends are acted on.
Support the recall procedure.
Prepare or assist in the generation, review and approval of SOPs.
Assist in the generation, review or approval of other technical documents i.e. batch documentation, specifications, material specifications, qualification documentation, validation documentation, technical agreements and technical memos.
Support customer enquiries and complaints procedure.
Ensure KPI's are prepared and trended for the monthly report, management review and annual product reviews
REQUIREMENTS
Life Science education of Master/Bachelor level
2-10 years of experience in QA
Experience as consultant/contractor of benefit
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
