Quality Control Technician
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Noord-Holland Netherlands.
- Quality Control testing
• Accountable for day to day testing activities in according with Site manufacturing planning and agreed lead times.
• Handling failure investigations.
• Documentation
• Stability:
• Outsourcing
• Qualification
• cGXP
• Regulatory authority inspections:
• Represent the department from a quality perspective to customers and professional.
+ Good knowledge of HPLC and other instruments operation
+ Regulatory authority inspections
+ Knowledge of cGXPs
+ Knowledge of relevant regulatory guidance’s
+ Ability to understand and execute against the Department Quality Management System
+ Ability to promote continuous process improvement/ efficiency
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
The Company
One of the largest pharmaceutical companies in the world.Role Description
- Support the value stream organizational structure, take care of all non-routine Quality Control activities.- Quality Control testing
Responsibilities
• Accountable for day to day testing activities in according with cGMP guidelines, Global Standard and local GMP as well as EHS SOP’s.• Accountable for day to day testing activities in according with Site manufacturing planning and agreed lead times.
• Handling failure investigations.
• Documentation
• Stability:
• Outsourcing
• Qualification
• cGXP
• Regulatory authority inspections:
• Represent the department from a quality perspective to customers and professional.
Requirements
+ HBO / University level (Pharmacy / Analytical Chemistry)+ Good knowledge of HPLC and other instruments operation
+ Regulatory authority inspections
+ Knowledge of cGXPs
+ Knowledge of relevant regulatory guidance’s
+ Ability to understand and execute against the Department Quality Management System
+ Ability to promote continuous process improvement/ efficiency
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
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