Ready to engineer precision in the data world? Join our client's cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow's breakthroughs.
Proclinical is seeking a detail-oriented and proactive individual to support the Manufacturing Science & Technology (MST) and Validation teams. In this role, you will contribute to data management, process improvement, documentation, and compliance activities to ensure efficient operations and adherence to quality and regulatory standards. This position offers an excellent opportunity to work in a dynamic environment and make meaningful contributions to critical projects.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
Ensure compliance with safety guidelines and regulations, including proper use of safety equipment and active participation in safety initiatives.
Contribute to the setup, maintenance, and validation of STATISTICA workspaces for automated data evaluation from systems such as LIMS and MES, ensuring data integrity and analysis accuracy.
Assist with document archiving activities, including preparation, organization, and transfer of documentation to the Scan Competence Center.
Support Validation and MST projects by performing data extraction, processing, analysis, reporting, and sample handling activities.
Update and maintain Standard Operating Procedures (SOPs), work instructions, forms, and other controlled documents within the MST and Validation departments.
Key Skills and Requirements:
A degree in pharmacy, pharmaceutical technology, biology, chemistry, or a related scientific field (Bachelor's, Master's, or PhD) OR equivalent industry experience.
Familiarity with Good Manufacturing Practices (GMP) is preferred.
Strong organizational skills and attention to detail.
Ability to manage and analyze data effectively.
Proficiency in maintaining and updating technical documentation.
A proactive approach to identifying and addressing safety risks.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.
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Proclinical is seeking a detail-oriented and proactive individual to support the Manufacturing Science & Technology (MST) and Validation teams. In this role, you will contribute to data management, process improvement, documentation, and compliance activities to ensure efficient operations and adherence to quality and regulatory standards. This position offers an excellent opportunity to work in a dynamic environment and make meaningful contributions to critical projects.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
Ensure compliance with safety guidelines and regulations, including proper use of safety equipment and active participation in safety initiatives.
Contribute to the setup, maintenance, and validation of STATISTICA workspaces for automated data evaluation from systems such as LIMS and MES, ensuring data integrity and analysis accuracy.
Assist with document archiving activities, including preparation, organization, and transfer of documentation to the Scan Competence Center.
Support Validation and MST projects by performing data extraction, processing, analysis, reporting, and sample handling activities.
Update and maintain Standard Operating Procedures (SOPs), work instructions, forms, and other controlled documents within the MST and Validation departments.
Key Skills and Requirements:
A degree in pharmacy, pharmaceutical technology, biology, chemistry, or a related scientific field (Bachelor's, Master's, or PhD) OR equivalent industry experience.
Familiarity with Good Manufacturing Practices (GMP) is preferred.
Strong organizational skills and attention to detail.
Ability to manage and analyze data effectively.
Proficiency in maintaining and updating technical documentation.
A proactive approach to identifying and addressing safety risks.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.
#J-18808-Ljbffr
Engineering Data Support Arbeitgeber: Proclinical Group
Proclinical ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, als Global Launch Manager in einer dynamischen und innovativen Umgebung in Zentraldeutschland zu arbeiten. Unsere Unternehmenskultur fördert Zusammenarbeit und Kreativität, während wir gleichzeitig auf individuelle Entwicklung und Wachstum unserer Mitarbeiter Wert legen. Genießen Sie attraktive Vorteile und die Chance, an globalen Strategien mitzuwirken, die den Erfolg unseres Unternehmens maßgeblich beeinflussen.
