- Junior
- Bureau à Porto
Career Opportunities: Quality Control Analyst (4316)Requisition ID 4316 - Posted - Portugal - Porto
The Position:
Ensures the execution of analytical (instrumental and physical and chemical) and documental work supporting Quality Control processes and activities.
Main Attributions and Responsibilities:
- Perform physical and chemical tests on raw materials, packaging materials, intermediates, bulk and finished products;
- Record all data, calculations and results and inform the responsible person of any out-of-specification or atypical result and collaborate in their investigation;
- Contribute to the proper maintenance of equipment and infrastructure and use it according to the established procedures and good practices in order to guarantee proper functioning and qualification status;
- Perform tasks under the scope of qualification and computerized system validation plans;
- Prepare and review technical documentation;
- Comply with GMP applicable to Quality Control activities;
- Comply with safety standards applicable to physicochemical and microbiology laboratories;
- Comply with the Policies, Standards and Procedures in place;
- Collaborate in all department activities as needed.
Preferential Requirements and Factors:
- Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar;
- Solid knowledge of instrumental analysis methods and wet chemistry;
- Solid knowledge of statistics applied to Quality Control (preferred);
- Strong computer and digital skills;
- Fluency in English;
- Team player.
“At Bial there is no such thing as "luck". There is commitment, dedication, and involvement with the Bial project and my team is part of this journey.”
Nuno Costa (Senior Manager Qualifications & Projects, Portugal)
JOIN US!
To know more about BIAL, visit us on www.bial.com. Follow us on LinkedIn and Facebook
The Position:
Ensures the execution of analytical (instrumental and physical and chemical) and documental work supporting Quality Control processes and activities.
Main Attributions and Responsibilities:
- Perform physical and chemical tests on raw materials, packaging materials, intermediates, bulk and finished products;
- Record all data, calculations and results and inform the responsible person of any out-of-specification or atypical result and collaborate in their investigation;
- Contribute to the proper maintenance of equipment and infrastructure and use it according to the established procedures and good practices in order to guarantee proper functioning and qualification status;
- Perform tasks under the scope of qualification and computerized system validation plans;
- Prepare and review technical documentation;
- Comply with GMP applicable to Quality Control activities;
- Comply with safety standards applicable to physicochemical and microbiology laboratories;
- Comply with the Policies, Standards and Procedures in place;
- Collaborate in all department activities as needed.
Preferential Requirements and Factors:
- Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar;
- Solid knowledge of instrumental analysis methods and wet chemistry;
- Solid knowledge of statistics applied to Quality Control (preferred);
- Strong computer and digital skills;
- Fluency in English;
- Team player.
“At Bial there is no such thing as "luck". There is commitment, dedication, and involvement with the Bial project and my team is part of this journey.”
Nuno Costa (Senior Manager Qualifications & Projects, Portugal)
JOIN US!
To know more about BIAL, visit us on www.bial.com. Follow us on LinkedIn and Facebook
The Position:
Ensures the execution of analytical (instrumental and physical and chemical) and documental work supporting Quality Control processes and activities.
Main Attributions and Responsibilities:
- Perform physical and chemical tests on raw materials, packaging materials, intermediates, bulk and finished products;
- Record all data, calculations and results and inform the responsible person of any out-of-specification or atypical result and collaborate in their investigation;
- Contribute to the proper maintenance of equipment and infrastructure and use it according to the established procedures and good practices in order to guarantee proper functioning and qualification status;
- Perform tasks under the scope of qualification and computerized system validation plans;
- Prepare and review technical documentation;
- Comply with GMP applicable to Quality Control activities;
- Comply with safety standards applicable to physicochemical and microbiology laboratories;
- Comply with the Policies, Standards and Procedures in place;
- Collaborate in all department activities as needed.
Preferential Requirements and Factors:
- Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar;
- Solid knowledge of instrumental analysis methods and wet chemistry;
- Solid knowledge of statistics applied to Quality Control (preferred);
- Strong computer and digital skills;
- Fluency in English;
- Team player.
“At Bial there is no such thing as "luck". There is commitment, dedication, and involvement with the Bial project and my team is part of this journey.”
Nuno Costa (Senior Manager Qualifications & Projects, Portugal)
JOIN US!
To know more about BIAL, visit us on www.bial.com. Follow us on LinkedIn and Facebook
The Position:
Ensures the execution of analytical (instrumental and physical and chemical) and documental work supporting Quality Control processes and activities.
Main Attributions and Responsibilities:
- Perform physical and chemical tests on raw materials, packaging materials, intermediates, bulk and finished products;
- Record all data, calculations and results and inform the responsible person of any out-of-specification or atypical result and collaborate in their investigation;
- Contribute to the proper maintenance of equipment and infrastructure and use it according to the established procedures and good practices in order to guarantee proper functioning and qualification status;
- Perform tasks under the scope of qualification and computerized system validation plans;
- Prepare and review technical documentation;
- Comply with GMP applicable to Quality Control activities;
- Comply with safety standards applicable to physicochemical and microbiology laboratories;
- Comply with the Policies, Standards and Procedures in place;
- Collaborate in all department activities as needed.
Preferential Requirements and Factors:
- Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar;
- Solid knowledge of instrumental analysis methods and wet chemistry;
- Solid knowledge of statistics applied to Quality Control (preferred);
- Strong computer and digital skills;
- Fluency in English;
- Team player.
“At Bial there is no such thing as "luck". There is commitment, dedication, and involvement with the Bial project and my team is part of this journey.”
Nuno Costa (Senior Manager Qualifications & Projects, Portugal)
JOIN US!
To know more about BIAL, visit us on www.bial.com. Follow us on LinkedIn and Facebook